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<thead> | <thead> | ||
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<li class="level1"><div class="li"> Packaging Mastermix</div> | <li class="level1"><div class="li"> Packaging Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> PEI Mastermix</div> | <li class="level1"><div class="li"> PEI Mastermix</div> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit22" id="section070617">07.06.17</h2> | <h2 class="sectionedit22" id="section070617">07.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit23" id="amaxa_electroporation">Amaxa electroporation</h3> | <h3 class="sectionedit23" id="amaxa_electroporation">Amaxa electroporation</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit24" id="production_of_lentivirus1">Production of Lentivirus</h3> | <h3 class="sectionedit24" id="production_of_lentivirus1">Production of Lentivirus</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit25" id="biorad_electroporation1">BioRad electroporation</h3> | <h3 class="sectionedit25" id="biorad_electroporation1">BioRad electroporation</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit26" id="section080617">08.06.17</h2> | <h2 class="sectionedit26" id="section080617">08.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit27" id="production_of_lentivirus2">Production of Lentivirus</h3> | <h3 class="sectionedit27" id="production_of_lentivirus2">Production of Lentivirus</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit28" id="flow_cytometry">Flow Cytometry</h3> | <h3 class="sectionedit28" id="flow_cytometry">Flow Cytometry</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit29" id="section090617">09.06.17</h2> | <h2 class="sectionedit29" id="section090617">09.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit30" id="lentiviral_transduction">Lentiviral transduction</h3> | <h3 class="sectionedit30" id="lentiviral_transduction">Lentiviral transduction</h3> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<thead> | <thead> | ||
<tr class="row0"> | <tr class="row0"> | ||
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</tr> | </tr> | ||
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<thead> | <thead> | ||
<tr class="row0"> | <tr class="row0"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit34" id="section100617">10.06.17</h2> | <h2 class="sectionedit34" id="section100617">10.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit35" id="biorad_electroporation2">BioRad electroporation</h3> | <h3 class="sectionedit35" id="biorad_electroporation2">BioRad electroporation</h3> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<thead> | <thead> | ||
<tr class="row0"> | <tr class="row0"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit38" id="section120617">12.06.17</h2> | <h2 class="sectionedit38" id="section120617">12.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit39" id="lentiviral_transduction1">Lentiviral transduction</h3> | <h3 class="sectionedit39" id="lentiviral_transduction1">Lentiviral transduction</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit40" id="flow_cytometry_for_biorad_electroporation_on_june_10th">Flow Cytometry for BioRad electroporation on June 10th</h3> | <h3 class="sectionedit40" id="flow_cytometry_for_biorad_electroporation_on_june_10th">Flow Cytometry for BioRad electroporation on June 10th</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit41" id="section130617">13.06.17</h2> | <h2 class="sectionedit41" id="section130617">13.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit42" id="flow_cytometry_for_lentiviral_infected_cells">Flow Cytometry for lentiviral infected cells</h3> | <h3 class="sectionedit42" id="flow_cytometry_for_lentiviral_infected_cells">Flow Cytometry for lentiviral infected cells</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit43" id="biorad_electroporation3">BioRad Electroporation</h3> | <h3 class="sectionedit43" id="biorad_electroporation3">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit45" id="section140617">14.06.17</h2> | <h2 class="sectionedit45" id="section140617">14.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit46" id="amaxa_electroporation1">Amaxa electroporation</h3> | <h3 class="sectionedit46" id="amaxa_electroporation1">Amaxa electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit47" id="flow_cytometry_for_biorad_electroporated_jk_cells">Flow Cytometry for BioRad electroporated JK cells</h3> | <h3 class="sectionedit47" id="flow_cytometry_for_biorad_electroporated_jk_cells">Flow Cytometry for BioRad electroporated JK cells</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit48" id="section150617">15.06.17</h2> | <h2 class="sectionedit48" id="section150617">15.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit49" id="flow_cytometry_for_biorad_electroporated_hut78_cells_and_amaxa_electroporated_t_cells">Flow Cytometry for BioRad electroporated Hut78 cells and Amaxa electroporated T cells</h3> | <h3 class="sectionedit49" id="flow_cytometry_for_biorad_electroporated_hut78_cells_and_amaxa_electroporated_t_cells">Flow Cytometry for BioRad electroporated Hut78 cells and Amaxa electroporated T cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit50" id="section160617">16.06.17</h2> | <h2 class="sectionedit50" id="section160617">16.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit51" id="mycoplasma_test_lentiviral_transduced_jurkat_and_hut78">Mycoplasma test(lentiviral transduced Jurkat and Hut78)</h3> | <h3 class="sectionedit51" id="mycoplasma_test_lentiviral_transduced_jurkat_and_hut78">Mycoplasma test(lentiviral transduced Jurkat and Hut78)</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit52" id="section170617">17.06.17</h2> | <h2 class="sectionedit52" id="section170617">17.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit53" id="biorad_electroporation_with_jk_cells">BioRad Electroporation with JK cells</h3> | <h3 class="sectionedit53" id="biorad_electroporation_with_jk_cells">BioRad Electroporation with JK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit55" id="pei_transfection_with_hek_cells">PEI transfection with HEK cells</h3> | <h3 class="sectionedit55" id="pei_transfection_with_hek_cells">PEI transfection with HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit57" id="section190617">19.06.17</h2> | <h2 class="sectionedit57" id="section190617">19.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit58" id="hypoxia_test_cocl2">Hypoxia test (CoCl2)</h3> | <h3 class="sectionedit58" id="hypoxia_test_cocl2">Hypoxia test (CoCl2)</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit59" id="biorad_electroporation4">BioRad Electroporation</h3> | <h3 class="sectionedit59" id="biorad_electroporation4">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit61" id="section200617">20.06.17</h2> | <h2 class="sectionedit61" id="section200617">20.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit62" id="biorad_electroporation5">BioRad electroporation</h3> | <h3 class="sectionedit62" id="biorad_electroporation5">BioRad electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit64" id="section210617">21.06.17</h2> | <h2 class="sectionedit64" id="section210617">21.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit65" id="mycoplasma-test_stock_cultures">Mycoplasma-Test (Stock cultures)</h3> | <h3 class="sectionedit65" id="mycoplasma-test_stock_cultures">Mycoplasma-Test (Stock cultures)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit66" id="flow_cytometry_biorad_on_jun19th">Flow Cytometry (BioRad on Jun.19th)</h3> | <h3 class="sectionedit66" id="flow_cytometry_biorad_on_jun19th">Flow Cytometry (BioRad on Jun.19th)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit67" id="section240617">24.06.17</h2> | <h2 class="sectionedit67" id="section240617">24.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit68" id="pei_transfection_pig17_013_for_hypoxia_test">PEI transfection (pIG17_013) for hypoxia test</h3> | <h3 class="sectionedit68" id="pei_transfection_pig17_013_for_hypoxia_test">PEI transfection (pIG17_013) for hypoxia test</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit69" id="section250617">25.06.17</h2> | <h2 class="sectionedit69" id="section250617">25.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit70" id="hypoxia_test_cocl21">Hypoxia test (CoCl2)</h3> | <h3 class="sectionedit70" id="hypoxia_test_cocl21">Hypoxia test (CoCl2)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<p> | <p> | ||
* Cell observation under fluorescence microscopy every hour after CoCl2 treatment | * Cell observation under fluorescence microscopy every hour after CoCl2 treatment | ||
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</div> | </div> | ||
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<h3 class="sectionedit72" id="biorad_electroporation6">BioRad Electroporation</h3> | <h3 class="sectionedit72" id="biorad_electroporation6">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> Flow cytometry after 24h. </div> | <li class="level1"><div class="li"> Flow cytometry after 24h. </div> | ||
</li> | </li> | ||
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</div> | </div> | ||
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<h2 class="sectionedit74" id="section260617">26.06.17</h2> | <h2 class="sectionedit74" id="section260617">26.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit75" id="hypoxia_test_cocl22">Hypoxia test (CoCl2)</h3> | <h3 class="sectionedit75" id="hypoxia_test_cocl22">Hypoxia test (CoCl2)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<p> | <p> | ||
<strong>2.Plate</strong> | <strong>2.Plate</strong> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit78" id="flow_cytometry_hypoxia_test_biorad">Flow Cytometry (Hypoxia test & BioRad)</h3> | <h3 class="sectionedit78" id="flow_cytometry_hypoxia_test_biorad">Flow Cytometry (Hypoxia test & BioRad)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit79" id="section270617">27.06.17</h2> | <h2 class="sectionedit79" id="section270617">27.06.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit80" id="biorad_electroporation8">BioRad Electroporation</h3> | <h3 class="sectionedit80" id="biorad_electroporation8">BioRad Electroporation</h3> | ||
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</div> | </div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit83" id="section280617">28.06.17</h2> | <h2 class="sectionedit83" id="section280617">28.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit84" id="flow_cytometryelectroporation_on_june_27th">Flow Cytometry: electroporation on June 27th</h3> | <h3 class="sectionedit84" id="flow_cytometryelectroporation_on_june_27th">Flow Cytometry: electroporation on June 27th</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit85" id="section290617">29.06.17</h2> | <h2 class="sectionedit85" id="section290617">29.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit86" id="production_of_lentivirus3">Production of Lentivirus</h3> | <h3 class="sectionedit86" id="production_of_lentivirus3">Production of Lentivirus</h3> | ||
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<li class="level1"><div class="li"> Packaging Mastermix</div> | <li class="level1"><div class="li"> Packaging Mastermix</div> | ||
</li> | </li> | ||
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<li class="level1"><div class="li"> PEI Mastermix</div> | <li class="level1"><div class="li"> PEI Mastermix</div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit91" id="section300617">30.06.17</h2> | <h2 class="sectionedit91" id="section300617">30.06.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit92" id="production_of_lentivirus4">Production of Lentivirus</h3> | <h3 class="sectionedit92" id="production_of_lentivirus4">Production of Lentivirus</h3> | ||
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<h3 class="sectionedit94" id="production_of_lentivirus5">Production of Lentivirus</h3> | <h3 class="sectionedit94" id="production_of_lentivirus5">Production of Lentivirus</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit95" id="lentiviral_transduction2">Lentiviral transduction</h3> | <h3 class="sectionedit95" id="lentiviral_transduction2">Lentiviral transduction</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit97" id="pei_transfection_with_hek_for_hypoxia_test">PEI transfection with HEK for Hypoxia Test</h3> | <h3 class="sectionedit97" id="pei_transfection_with_hek_for_hypoxia_test">PEI transfection with HEK for Hypoxia Test</h3> | ||
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</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit99" id="biorad_electroporationrepeat_pgfp_transfection">BioRad Electroporation: Repeat pGFP transfection</h3> | <h3 class="sectionedit99" id="biorad_electroporationrepeat_pgfp_transfection">BioRad Electroporation: Repeat pGFP transfection</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit101" id="section020717">02.07.17</h2> | <h2 class="sectionedit101" id="section020717">02.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit102" id="cocl2_treatment_with_jurkat_cells">CoCl2 treatment with Jurkat cells</h3> | <h3 class="sectionedit102" id="cocl2_treatment_with_jurkat_cells">CoCl2 treatment with Jurkat cells</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit103" id="repeat_hypoxia_test_24h_after_pei">Repeat Hypoxia test (24h after PEI)</h3> | <h3 class="sectionedit103" id="repeat_hypoxia_test_24h_after_pei">Repeat Hypoxia test (24h after PEI)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit104" id="section030717">03.07.17</h2> | <h2 class="sectionedit104" id="section030717">03.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit105" id="repeat_hypoxia_test_48h_after_pei">Repeat Hypoxia test (48h after PEI)</h3> | <h3 class="sectionedit105" id="repeat_hypoxia_test_48h_after_pei">Repeat Hypoxia test (48h after PEI)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit106" id="section040717">04.07.17</h2> | <h2 class="sectionedit106" id="section040717">04.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit107" id="lentiviral_transduction_plenti-crispr_from_ag_cathomen">Lentiviral transduction (pLenti-CRISPR from AG Cathomen)</h3> | <h3 class="sectionedit107" id="lentiviral_transduction_plenti-crispr_from_ag_cathomen">Lentiviral transduction (pLenti-CRISPR from AG Cathomen)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit108" id="biorad_electroporationrepeat_pgfp_transfection1">BioRad Electroporation: Repeat pGFP transfection</h3> | <h3 class="sectionedit108" id="biorad_electroporationrepeat_pgfp_transfection1">BioRad Electroporation: Repeat pGFP transfection</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit110" id="section050717">05.07.17</h2> | <h2 class="sectionedit110" id="section050717">05.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit111" id="pei_transfection_pig17_022_and_pig17_023_for_ctla-4_promoter_test">PEI transfection (pIG17_022 and pIG17_023) for CTLA-4 promoter test</h3> | <h3 class="sectionedit111" id="pei_transfection_pig17_022_and_pig17_023_for_ctla-4_promoter_test">PEI transfection (pIG17_022 and pIG17_023) for CTLA-4 promoter test</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit112" id="flow_cytometry1">Flow Cytometry</h3> | <h3 class="sectionedit112" id="flow_cytometry1">Flow Cytometry</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit113" id="section060717">06.07.17</h2> | <h2 class="sectionedit113" id="section060717">06.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit114" id="prepare_cells_for_lentivirus-production">Prepare cells for lentivirus-production</h3> | <h3 class="sectionedit114" id="prepare_cells_for_lentivirus-production">Prepare cells for lentivirus-production</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit115" id="vegf_induction_with_modeling_group">VEGF induction with Modeling group</h3> | <h3 class="sectionedit115" id="vegf_induction_with_modeling_group">VEGF induction with Modeling group</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit116" id="section070717">07.07.17</h2> | <h2 class="sectionedit116" id="section070717">07.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit117" id="lentivirus_pig17_119_production_in_hek_cells">Lentivirus(pIG17_119) production in HEK cells</h3> | <h3 class="sectionedit117" id="lentivirus_pig17_119_production_in_hek_cells">Lentivirus(pIG17_119) production in HEK cells</h3> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</tr> | </tr> | ||
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<li class="level1"><div class="li"> Packaging Mastermix</div> | <li class="level1"><div class="li"> Packaging Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> PEI Mastermix</div> | <li class="level1"><div class="li"> PEI Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit122" id="section080717">08.07.17</h2> | <h2 class="sectionedit122" id="section080717">08.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit123" id="lentivirus_pig17_119_production_in_hek_cells1">Lentivirus(pIG17_119) production in HEK cells</h3> | <h3 class="sectionedit123" id="lentivirus_pig17_119_production_in_hek_cells1">Lentivirus(pIG17_119) production in HEK cells</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit124" id="biorad_electroporation9">BioRad electroporation</h3> | <h3 class="sectionedit124" id="biorad_electroporation9">BioRad electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit125" id="section090717">09.07.17</h2> | <h2 class="sectionedit125" id="section090717">09.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit126" id="lentivirus_pig17_119_production_in_hek_cells2">Lentivirus(pIG17_119) production in HEK cells</h3> | <h3 class="sectionedit126" id="lentivirus_pig17_119_production_in_hek_cells2">Lentivirus(pIG17_119) production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit127" id="section100717">10.07.17</h2> | <h2 class="sectionedit127" id="section100717">10.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit128" id="lentivirus_pig17_119_production_in_hek_cells3">Lentivirus(pIG17_119) production in HEK cells</h3> | <h3 class="sectionedit128" id="lentivirus_pig17_119_production_in_hek_cells3">Lentivirus(pIG17_119) production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit129" id="section110717">11.07.17</h2> | <h2 class="sectionedit129" id="section110717">11.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit130" id="pei_transfection_ctla-4_test">PEI transfection (CTLA-4 Test)</h3> | <h3 class="sectionedit130" id="pei_transfection_ctla-4_test">PEI transfection (CTLA-4 Test)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit131" id="lentiviral_transduction_pig17_119_of_jurkat_cells">Lentiviral transduction (pIG17_119) of Jurkat cells</h3> | <h3 class="sectionedit131" id="lentiviral_transduction_pig17_119_of_jurkat_cells">Lentiviral transduction (pIG17_119) of Jurkat cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit132" id="section120717">12.07.17</h2> | <h2 class="sectionedit132" id="section120717">12.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit133" id="biorad_electroporation10">BioRad electroporation</h3> | <h3 class="sectionedit133" id="biorad_electroporation10">BioRad electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit135" id="section140717">14.07.17</h2> | <h2 class="sectionedit135" id="section140717">14.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit136" id="lentivirus_pig17_121_production_in_hek_cells">Lentivirus(pIG17_121) production in HEK cells</h3> | <h3 class="sectionedit136" id="lentivirus_pig17_121_production_in_hek_cells">Lentivirus(pIG17_121) production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<thead> | <thead> | ||
<tr class="row0"> | <tr class="row0"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> Packaging Mastermix</div> | <li class="level1"><div class="li"> Packaging Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> PEI Mastermix</div> | <li class="level1"><div class="li"> PEI Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
− | <div class='secedit editbutton_section editbutton_136' | + | <div class='secedit editbutton_section editbutton_136'></div> |
<h3 class="sectionedit141" id="biorad_electroporation11">BioRad electroporation</h3> | <h3 class="sectionedit141" id="biorad_electroporation11">BioRad electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit143" id="section150717">15.07.17</h2> | <h2 class="sectionedit143" id="section150717">15.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit144" id="collect_virus_pig17_121">collect virus (pIG17_121)</h3> | <h3 class="sectionedit144" id="collect_virus_pig17_121">collect virus (pIG17_121)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
</div> | </div> | ||
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<h3 class="sectionedit145" id="flow_cytometry_biorad_7_14">flow cytometry (BioRad 7/14)</h3> | <h3 class="sectionedit145" id="flow_cytometry_biorad_7_14">flow cytometry (BioRad 7/14)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
</div> | </div> | ||
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<h2 class="sectionedit146" id="section160717">16.07.17</h2> | <h2 class="sectionedit146" id="section160717">16.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit147" id="pei_transfection">PEI transfection</h3> | <h3 class="sectionedit147" id="pei_transfection">PEI transfection</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit148" id="biorad_electroporation12">BioRad electroporation</h3> | <h3 class="sectionedit148" id="biorad_electroporation12">BioRad electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit150" id="section170717">17.07.17</h2> | <h2 class="sectionedit150" id="section170717">17.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit151" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | <h3 class="sectionedit151" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit152" id="flow_cytometry2">Flow Cytometry</h3> | <h3 class="sectionedit152" id="flow_cytometry2">Flow Cytometry</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit153" id="section180717">18.07.17</h2> | <h2 class="sectionedit153" id="section180717">18.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit154" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen1">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | <h3 class="sectionedit154" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen1">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit155" id="lentiviral_transduction3">Lentiviral transduction</h3> | <h3 class="sectionedit155" id="lentiviral_transduction3">Lentiviral transduction</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit156" id="biorad_electroporation13">BioRad electroporation</h3> | <h3 class="sectionedit156" id="biorad_electroporation13">BioRad electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit158" id="pei_transfection_ctla-4_test1">PEI transfection (CTLA-4 Test)</h3> | <h3 class="sectionedit158" id="pei_transfection_ctla-4_test1">PEI transfection (CTLA-4 Test)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit159" id="pei_transfection_hypoxia_test_with_cocl2">PEI transfection (hypoxia test with CoCl2)</h3> | <h3 class="sectionedit159" id="pei_transfection_hypoxia_test_with_cocl2">PEI transfection (hypoxia test with CoCl2)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit160" id="section190717">19.07.17</h2> | <h2 class="sectionedit160" id="section190717">19.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit161" id="concentrate_the_viruses_pig17_119_and_pig17_121">Concentrate the viruses (pIG17_119 and pIG17_121)</h3> | <h3 class="sectionedit161" id="concentrate_the_viruses_pig17_119_and_pig17_121">Concentrate the viruses (pIG17_119 and pIG17_121)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit162" id="lentiviral_transduction4">Lentiviral transduction</h3> | <h3 class="sectionedit162" id="lentiviral_transduction4">Lentiviral transduction</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit163" id="cocl2_treatment_24h_after_pei">CoCl2 treatment (24h after PEI)</h3> | <h3 class="sectionedit163" id="cocl2_treatment_24h_after_pei">CoCl2 treatment (24h after PEI)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit164" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen2">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | <h3 class="sectionedit164" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen2">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit165" id="flow_cytometry_biorad_on_july_20th">Flow Cytometry (BioRad on July 20th)</h3> | <h3 class="sectionedit165" id="flow_cytometry_biorad_on_july_20th">Flow Cytometry (BioRad on July 20th)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit166" id="section200717">20.07.17</h2> | <h2 class="sectionedit166" id="section200717">20.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit167" id="cocl2_treatment_48h_after_pei">CoCl2 treatment (48h after PEI)</h3> | <h3 class="sectionedit167" id="cocl2_treatment_48h_after_pei">CoCl2 treatment (48h after PEI)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit168" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen3">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | <h3 class="sectionedit168" id="hypoxia_test_in_hypoxia_incubator_ag_cathomen3">Hypoxia Test in hypoxia incubator (AG Cathomen)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit169" id="section210717">21.07.17</h2> | <h2 class="sectionedit169" id="section210717">21.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit170" id="biorad_electroporation_knock-out_plasmids">BioRad Electroporation (Knock-Out plasmids)</h3> | <h3 class="sectionedit170" id="biorad_electroporation_knock-out_plasmids">BioRad Electroporation (Knock-Out plasmids)</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit172" id="section220717">22.07.17</h2> | <h2 class="sectionedit172" id="section220717">22.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit173" id="lentivirus_pig17_119_and_pig17_121_production_in_hek_cells">Lentivirus(pIG17_119 and pIG17_121) production in HEK cells</h3> | <h3 class="sectionedit173" id="lentivirus_pig17_119_and_pig17_121_production_in_hek_cells">Lentivirus(pIG17_119 and pIG17_121) production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<thead> | <thead> | ||
<tr class="row0"> | <tr class="row0"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> Packaging Mastermix</div> | <li class="level1"><div class="li"> Packaging Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> PEI Mastermix</div> | <li class="level1"><div class="li"> PEI Mastermix</div> | ||
</li> | </li> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit178" id="section2207171">22.07.17</h2> | <h2 class="sectionedit178" id="section2207171">22.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit179" id="flow_cytometrybiorad_electroporation_7_21">Flow Cytometry: BioRad Electroporation 7/21</h3> | <h3 class="sectionedit179" id="flow_cytometrybiorad_electroporation_7_21">Flow Cytometry: BioRad Electroporation 7/21</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit180" id="lentivirus_pig17_119_and_pig17_121_production_in_hek_cells1">Lentivirus(pIG17_119 and pIG17_121) production in HEK cells</h3> | <h3 class="sectionedit180" id="lentivirus_pig17_119_and_pig17_121_production_in_hek_cells1">Lentivirus(pIG17_119 and pIG17_121) production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit181" id="section230717">23.07.17</h2> | <h2 class="sectionedit181" id="section230717">23.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit182" id="lentivirus_pig17_119_and_pig17_121_production_in_hek_cells2">Lentivirus(pIG17_119 and pIG17_121) production in HEK cells</h3> | <h3 class="sectionedit182" id="lentivirus_pig17_119_and_pig17_121_production_in_hek_cells2">Lentivirus(pIG17_119 and pIG17_121) production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit183" id="section240717">24.07.17</h2> | <h2 class="sectionedit183" id="section240717">24.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit184" id="mycoplamsa_test">Mycoplamsa Test</h3> | <h3 class="sectionedit184" id="mycoplamsa_test">Mycoplamsa Test</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit185" id="section250717">25.07.17</h2> | <h2 class="sectionedit185" id="section250717">25.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit186" id="pei_transfection_of_cho_cellshypoxia_tet_system">PEI transfection of CHO cells: Hypoxia & Tet system</h3> | <h3 class="sectionedit186" id="pei_transfection_of_cho_cellshypoxia_tet_system">PEI transfection of CHO cells: Hypoxia & Tet system</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit188" id="tetracycline_induction_of_cho">Tetracycline induction of CHO</h3> | <h3 class="sectionedit188" id="tetracycline_induction_of_cho">Tetracycline induction of CHO</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit189" id="pei_transfection_of_hek_cellshypoxia">PEI transfection of HEK cells: Hypoxia</h3> | <h3 class="sectionedit189" id="pei_transfection_of_hek_cellshypoxia">PEI transfection of HEK cells: Hypoxia</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit191" id="section260717">26.07.17</h2> | <h2 class="sectionedit191" id="section260717">26.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit192" id="cocl2_treatment">CoCl2 treatment</h3> | <h3 class="sectionedit192" id="cocl2_treatment">CoCl2 treatment</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit194" id="section270717">27.07.17</h2> | <h2 class="sectionedit194" id="section270717">27.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit195" id="seap_assay_with_hek_cells">SEAP assay with HEK cells</h3> | <h3 class="sectionedit195" id="seap_assay_with_hek_cells">SEAP assay with HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit196" id="replace_stock_cultures_with_new_culture_from_toolbox">Replace Stock cultures with new culture from Toolbox</h3> | <h3 class="sectionedit196" id="replace_stock_cultures_with_new_culture_from_toolbox">Replace Stock cultures with new culture from Toolbox</h3> | ||
<div class="level3"> | <div class="level3"> | ||
</div> | </div> | ||
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<h2 class="sectionedit197" id="section310717">31.07.17</h2> | <h2 class="sectionedit197" id="section310717">31.07.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit198" id="mycoplasma_testnew_hek_stock">Mycoplasma Test: New HEK stock</h3> | <h3 class="sectionedit198" id="mycoplasma_testnew_hek_stock">Mycoplasma Test: New HEK stock</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit199" id="section010817">01.08.17</h2> | <h2 class="sectionedit199" id="section010817">01.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit200" id="biorad_electroporation14">BioRad Electroporation</h3> | <h3 class="sectionedit200" id="biorad_electroporation14">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit202" id="pei_transfectionhypoxia_-_seap_assay_in_hek_cells">PEI transfection: Hypoxia - SEAP assay in HEK cells</h3> | <h3 class="sectionedit202" id="pei_transfectionhypoxia_-_seap_assay_in_hek_cells">PEI transfection: Hypoxia - SEAP assay in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<p> | <p> | ||
Due to the concentrations and volumes in the tubes for each approach two were used. | Due to the concentrations and volumes in the tubes for each approach two were used. | ||
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<h2 class="sectionedit204" id="section020817">02.08.17</h2> | <h2 class="sectionedit204" id="section020817">02.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit205" id="flow_cytometry_of_biorad_electroporation_8_1ko_plasmids">Flow Cytometry of BioRad Electroporation (8/1): KO plasmids</h3> | <h3 class="sectionedit205" id="flow_cytometry_of_biorad_electroporation_8_1ko_plasmids">Flow Cytometry of BioRad Electroporation (8/1): KO plasmids</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit206" id="addition_of_cocl2hypoxia_-_seap_assay_in_hek_cells">Addition of CoCl2: Hypoxia - SEAP assay in HEK cells</h3> | <h3 class="sectionedit206" id="addition_of_cocl2hypoxia_-_seap_assay_in_hek_cells">Addition of CoCl2: Hypoxia - SEAP assay in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit208" id="lentivirus_production_in_hek_cellsmock_knock-down_plasmid_114_115_116_pig17_119_pig17_121">Lentivirus production in HEK cells: Mock, Knock-down plasmid (114,115,116), pIG17_119, pIG17_121</h3> | <h3 class="sectionedit208" id="lentivirus_production_in_hek_cellsmock_knock-down_plasmid_114_115_116_pig17_119_pig17_121">Lentivirus production in HEK cells: Mock, Knock-down plasmid (114,115,116), pIG17_119, pIG17_121</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</table></div> | </table></div> | ||
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<thead> | <thead> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> Packaging Mastermix</div> | <li class="level1"><div class="li"> Packaging Mastermix</div> | ||
</li> | </li> | ||
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</table></div> | </table></div> | ||
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<p> | <p> | ||
<strong>Follow our protocol of PEI transfection</strong> | <strong>Follow our protocol of PEI transfection</strong> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit213" id="section030817">03.08.17</h2> | <h2 class="sectionedit213" id="section030817">03.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit214" id="hypoxia_-_seap_assay_in_hek_cells">Hypoxia - SEAP assay in HEK cells</h3> | <h3 class="sectionedit214" id="hypoxia_-_seap_assay_in_hek_cells">Hypoxia - SEAP assay in HEK cells</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit215" id="section050817">05.08.17</h2> | <h2 class="sectionedit215" id="section050817">05.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit216" id="lentiviral_transduction5">Lentiviral Transduction</h3> | <h3 class="sectionedit216" id="lentiviral_transduction5">Lentiviral Transduction</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit217" id="puromycin_killing_curve">Puromycin killing curve</h3> | <h3 class="sectionedit217" id="puromycin_killing_curve">Puromycin killing curve</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit219" id="section060817">06.08.17</h2> | <h2 class="sectionedit219" id="section060817">06.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit220" id="pei_for_hre-seap_and_cmv-seaprepetition_of_the_seap_assay">PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay</h3> | <h3 class="sectionedit220" id="pei_for_hre-seap_and_cmv-seaprepetition_of_the_seap_assay">PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<thead> | <thead> | ||
<tr class="row0"> | <tr class="row0"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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<li class="level1"><div class="li"> Per Approach: 9µg DNA, 2 mio JK cells</div> | <li class="level1"><div class="li"> Per Approach: 9µg DNA, 2 mio JK cells</div> | ||
</li> | </li> | ||
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</div> | </div> | ||
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<h3 class="sectionedit223" id="biorad_electroporation15">BioRad Electroporation</h3> | <h3 class="sectionedit223" id="biorad_electroporation15">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit225" id="section070817">07.08.17</h2> | <h2 class="sectionedit225" id="section070817">07.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit226" id="pei_for_hre-seap_and_cmv-seaprepetition_of_the_seap_assay1">PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay</h3> | <h3 class="sectionedit226" id="pei_for_hre-seap_and_cmv-seaprepetition_of_the_seap_assay1">PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit228" id="section080817">08.08.17</h2> | <h2 class="sectionedit228" id="section080817">08.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit229" id="lentivirus_production_in_hek_cellsmock_pig17_133_pig17_119_pig17_121">Lentivirus production in HEK cells: Mock, pIG17_133, pIG17_119, pIG17_121</h3> | <h3 class="sectionedit229" id="lentivirus_production_in_hek_cellsmock_pig17_133_pig17_119_pig17_121">Lentivirus production in HEK cells: Mock, pIG17_133, pIG17_119, pIG17_121</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit230" id="pei_for_hre-seap_and_cmv-seaprepetition_of_the_seap_assay2">PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay</h3> | <h3 class="sectionedit230" id="pei_for_hre-seap_and_cmv-seaprepetition_of_the_seap_assay2">PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit231" id="section100817">10.08.17</h2> | <h2 class="sectionedit231" id="section100817">10.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit232" id="lentiviral_transduction6">Lentiviral transduction</h3> | <h3 class="sectionedit232" id="lentiviral_transduction6">Lentiviral transduction</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit233" id="cell_sortingko-plasmid_transfected_cells">Cell Sorting: KO-plasmid transfected cells</h3> | <h3 class="sectionedit233" id="cell_sortingko-plasmid_transfected_cells">Cell Sorting: KO-plasmid transfected cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit234" id="section110817">11.08.17</h2> | <h2 class="sectionedit234" id="section110817">11.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit235" id="biorad_electroporation16">BioRad Electroporation</h3> | <h3 class="sectionedit235" id="biorad_electroporation16">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit237" id="puromycin_killing_curve1">Puromycin killing curve</h3> | <h3 class="sectionedit237" id="puromycin_killing_curve1">Puromycin killing curve</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit238" id="puromycin_addition_to_the_electroplated_ko_kit_cells">Puromycin addition to the electroplated KO Kit cells</h3> | <h3 class="sectionedit238" id="puromycin_addition_to_the_electroplated_ko_kit_cells">Puromycin addition to the electroplated KO Kit cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit239" id="section120817">12.08.17</h2> | <h2 class="sectionedit239" id="section120817">12.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit240" id="puromycinelectroplated_ko_kit_cells">Puromycin: electroplated KO Kit cells</h3> | <h3 class="sectionedit240" id="puromycinelectroplated_ko_kit_cells">Puromycin: electroplated KO Kit cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit241" id="section140817">14.08.17</h2> | <h2 class="sectionedit241" id="section140817">14.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit242" id="peihre-seap_pww56">PEI: HRE-SEAP, pWW56</h3> | <h3 class="sectionedit242" id="peihre-seap_pww56">PEI: HRE-SEAP, pWW56</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h2 class="sectionedit244" id="section150817">15.08.17</h2> | <h2 class="sectionedit244" id="section150817">15.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit245" id="seap">SEAP</h3> | <h3 class="sectionedit245" id="seap">SEAP</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit247" id="electroporated_ko_kit_cells">Electroporated KO Kit cells</h3> | <h3 class="sectionedit247" id="electroporated_ko_kit_cells">Electroporated KO Kit cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h3 class="sectionedit248" id="biorad_electroporation17">BioRad Electroporation</h3> | <h3 class="sectionedit248" id="biorad_electroporation17">BioRad Electroporation</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</tr> | </tr> | ||
</table></div> | </table></div> | ||
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</div> | </div> | ||
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<h3 class="sectionedit250" id="lentivirus_production_in_hek_cells">Lentivirus Production in HEK cells</h3> | <h3 class="sectionedit250" id="lentivirus_production_in_hek_cells">Lentivirus Production in HEK cells</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit251" id="section160817">16.08.17</h2> | <h2 class="sectionedit251" id="section160817">16.08.17</h2> | ||
<div class="level2"> | <div class="level2"> | ||
</div> | </div> | ||
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<h3 class="sectionedit252" id="seap1">SEAP</h3> | <h3 class="sectionedit252" id="seap1">SEAP</h3> | ||
<div class="level3"> | <div class="level3"> | ||
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</div> | </div> | ||
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<h2 class="sectionedit253" id="section170817">17.08.17</h2> | <h2 class="sectionedit253" id="section170817">17.08.17</h2> | ||
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<h3 class="sectionedit254" id="lentiviral_transduction_with_virus-medium">Lentiviral Transduction with virus-medium</h3> | <h3 class="sectionedit254" id="lentiviral_transduction_with_virus-medium">Lentiviral Transduction with virus-medium</h3> | ||
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<h2 class="sectionedit255" id="section230817">23.08.17</h2> | <h2 class="sectionedit255" id="section230817">23.08.17</h2> | ||
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<h3 class="sectionedit256" id="pei_transfection_of_hek_cells_for_lentivirus_production">PEI transfection of HEK cells for lentivirus production</h3> | <h3 class="sectionedit256" id="pei_transfection_of_hek_cells_for_lentivirus_production">PEI transfection of HEK cells for lentivirus production</h3> | ||
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<h2 class="sectionedit257" id="section250817">25.08.17</h2> | <h2 class="sectionedit257" id="section250817">25.08.17</h2> | ||
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<h3 class="sectionedit258" id="concentrate_virus_pig17_130">Concentrate virus (pIG17_130)</h3> | <h3 class="sectionedit258" id="concentrate_virus_pig17_130">Concentrate virus (pIG17_130)</h3> | ||
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<h2 class="sectionedit259" id="section260817">26.08.17</h2> | <h2 class="sectionedit259" id="section260817">26.08.17</h2> | ||
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<h3 class="sectionedit260" id="lentiviral_transduction_pig17_130">Lentiviral Transduction (pIG17_130)</h3> | <h3 class="sectionedit260" id="lentiviral_transduction_pig17_130">Lentiviral Transduction (pIG17_130)</h3> | ||
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<h2 class="sectionedit261" id="section300817">30.08.17</h2> | <h2 class="sectionedit261" id="section300817">30.08.17</h2> | ||
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<h3 class="sectionedit262" id="pei_transfection_of_hek_cells_for_lentivirus_production_133_134">PEI transfection of HEK cells for lentivirus production (133&134)</h3> | <h3 class="sectionedit262" id="pei_transfection_of_hek_cells_for_lentivirus_production_133_134">PEI transfection of HEK cells for lentivirus production (133&134)</h3> | ||
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<h2 class="sectionedit263" id="section020917">02.09.17</h2> | <h2 class="sectionedit263" id="section020917">02.09.17</h2> | ||
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<h3 class="sectionedit264" id="pei_transfection_of_hek_cells_for_lentivirus_production_132">PEI transfection of HEK cells for lentivirus production (132)</h3> | <h3 class="sectionedit264" id="pei_transfection_of_hek_cells_for_lentivirus_production_132">PEI transfection of HEK cells for lentivirus production (132)</h3> | ||
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<h2 class="sectionedit265" id="section040917">04.09.17</h2> | <h2 class="sectionedit265" id="section040917">04.09.17</h2> | ||
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<h3 class="sectionedit266" id="biorad_electroporation18">BioRad Electroporation</h3> | <h3 class="sectionedit266" id="biorad_electroporation18">BioRad Electroporation</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit268" id="section050917">05.09.17</h2> | <h2 class="sectionedit268" id="section050917">05.09.17</h2> | ||
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<h2 class="sectionedit269" id="section060917">06.09.17</h2> | <h2 class="sectionedit269" id="section060917">06.09.17</h2> | ||
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<h2 class="sectionedit270" id="section070917">07.09.17</h2> | <h2 class="sectionedit270" id="section070917">07.09.17</h2> | ||
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<h3 class="sectionedit271" id="set-up_for_pig17_031_-_hypoxia">Set-up for pIG17_031 - hypoxia</h3> | <h3 class="sectionedit271" id="set-up_for_pig17_031_-_hypoxia">Set-up for pIG17_031 - hypoxia</h3> | ||
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<p> | <p> | ||
. | . | ||
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<h3 class="sectionedit273" id="set-up_for_pig17_034_-_ph">Set-up for pIG17_034 - pH</h3> | <h3 class="sectionedit273" id="set-up_for_pig17_034_-_ph">Set-up for pIG17_034 - pH</h3> | ||
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<li class="level1"><div class="li"> 6 well plate with 3ml RPMI and the same concentration of lactate or NaOH as in the 96 well plate but without cells</div> | <li class="level1"><div class="li"> 6 well plate with 3ml RPMI and the same concentration of lactate or NaOH as in the 96 well plate but without cells</div> | ||
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<h3 class="sectionedit275" id="set-up_for_pig17_037_-_vegf">Set-up for pIG17_037 - VEGF</h3> | <h3 class="sectionedit275" id="set-up_for_pig17_037_-_vegf">Set-up for pIG17_037 - VEGF</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit277" id="section270817070917">27.08.17 - 07.09.17</h2> | <h2 class="sectionedit277" id="section270817070917">27.08.17 - 07.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit278" id="neomycin_killing_curve_of_jurkat_cells">Neomycin killing curve of Jurkat cells</h3> | <h3 class="sectionedit278" id="neomycin_killing_curve_of_jurkat_cells">Neomycin killing curve of Jurkat cells</h3> | ||
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<h2 class="sectionedit279" id="section110917">11.09.17</h2> | <h2 class="sectionedit279" id="section110917">11.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit280" id="pei_transfection_of_hek_cells_for_lenvirus_production">PEI transfection of HEK cells for lenvirus production</h3> | <h3 class="sectionedit280" id="pei_transfection_of_hek_cells_for_lenvirus_production">PEI transfection of HEK cells for lenvirus production</h3> | ||
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<h3 class="sectionedit281" id="viafect_-_new_testing">Viafect - new testing</h3> | <h3 class="sectionedit281" id="viafect_-_new_testing">Viafect - new testing</h3> | ||
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<h2 class="sectionedit282" id="section150917">15.09.17</h2> | <h2 class="sectionedit282" id="section150917">15.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit283" id="pei_transfection_of_hek_cells_for_lenvirus_production1">PEI transfection of HEK cells for lenvirus production</h3> | <h3 class="sectionedit283" id="pei_transfection_of_hek_cells_for_lenvirus_production1">PEI transfection of HEK cells for lenvirus production</h3> | ||
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<h2 class="sectionedit284" id="section200917">20.09.17</h2> | <h2 class="sectionedit284" id="section200917">20.09.17</h2> | ||
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<h3 class="sectionedit285" id="pei_transfection_of_hek_cells_for_lenvirus_production2">PEI transfection of HEK cells for lenvirus production</h3> | <h3 class="sectionedit285" id="pei_transfection_of_hek_cells_for_lenvirus_production2">PEI transfection of HEK cells for lenvirus production</h3> | ||
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<h2 class="sectionedit286" id="section210917">21.09.17</h2> | <h2 class="sectionedit286" id="section210917">21.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit287" id="pei_transfection_of_hek_cells_for_seap_assay">PEI transfection of HEK cells for SEAP assay</h3> | <h3 class="sectionedit287" id="pei_transfection_of_hek_cells_for_seap_assay">PEI transfection of HEK cells for SEAP assay</h3> | ||
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<h2 class="sectionedit288" id="section220917">22.09.17</h2> | <h2 class="sectionedit288" id="section220917">22.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit289" id="seap_assay">SEAP assay</h3> | <h3 class="sectionedit289" id="seap_assay">SEAP assay</h3> | ||
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<h2 class="sectionedit290" id="section230917">23.09.17</h2> | <h2 class="sectionedit290" id="section230917">23.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit291" id="seap_assay1">SEAP assay</h3> | <h3 class="sectionedit291" id="seap_assay1">SEAP assay</h3> | ||
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<h2 class="sectionedit292" id="section240917">24.09.17</h2> | <h2 class="sectionedit292" id="section240917">24.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit293" id="pei_transfection_of_hek_cells_for_lenvirus_production3">PEI transfection of HEK cells for lenvirus production</h3> | <h3 class="sectionedit293" id="pei_transfection_of_hek_cells_for_lenvirus_production3">PEI transfection of HEK cells for lenvirus production</h3> | ||
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<h2 class="sectionedit294" id="section2409171">24.09.17</h2> | <h2 class="sectionedit294" id="section2409171">24.09.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit295" id="hre_testing_with_stable_hek_cell_lines">HRE testing with stable HEK cell lines</h3> | <h3 class="sectionedit295" id="hre_testing_with_stable_hek_cell_lines">HRE testing with stable HEK cell lines</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit296" id="section041017">04.10.17</h2> | <h2 class="sectionedit296" id="section041017">04.10.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit297" id="pei_transfection_of_hek_cells_for_lenvirus_production4">PEI transfection of HEK cells for lenvirus production</h3> | <h3 class="sectionedit297" id="pei_transfection_of_hek_cells_for_lenvirus_production4">PEI transfection of HEK cells for lenvirus production</h3> | ||
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<h2 class="sectionedit298" id="section091017">09.10.17</h2> | <h2 class="sectionedit298" id="section091017">09.10.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit299" id="cfp_test">CFP test</h3> | <h3 class="sectionedit299" id="cfp_test">CFP test</h3> | ||
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<h3 class="sectionedit300" id="cre_test_in_jurkat_cells">CRE Test in Jurkat cells</h3> | <h3 class="sectionedit300" id="cre_test_in_jurkat_cells">CRE Test in Jurkat cells</h3> | ||
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<h2 class="sectionedit301" id="section101017">10.10.17</h2> | <h2 class="sectionedit301" id="section101017">10.10.17</h2> | ||
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</div> | </div> | ||
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<h3 class="sectionedit302" id="hre_test_in_jurkat_cells">HRE Test in Jurkat cells</h3> | <h3 class="sectionedit302" id="hre_test_in_jurkat_cells">HRE Test in Jurkat cells</h3> | ||
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</div> | </div> | ||
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<h3 class="sectionedit303" id="hre_test_in_hek_cells">HRE Test in HEK cells</h3> | <h3 class="sectionedit303" id="hre_test_in_hek_cells">HRE Test in HEK cells</h3> | ||
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</div> | </div> | ||
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<h2 class="sectionedit304" id="section121017">12.10.17</h2> | <h2 class="sectionedit304" id="section121017">12.10.17</h2> | ||
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<h3 class="sectionedit305" id="cre_test_in_hek_cells">CRE Test in HEK cells</h3> | <h3 class="sectionedit305" id="cre_test_in_hek_cells">CRE Test in HEK cells</h3> | ||
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<h3 class="sectionedit306" id="cre_test_in_jurkat_cells1">CRE Test in Jurkat cells</h3> | <h3 class="sectionedit306" id="cre_test_in_jurkat_cells1">CRE Test in Jurkat cells</h3> | ||
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<h3 class="sectionedit307" id="vegf_test_in_hek_cells">VEGF Test in HEK cells</h3> | <h3 class="sectionedit307" id="vegf_test_in_hek_cells">VEGF Test in HEK cells</h3> | ||
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Revision as of 12:20, 19 October 2017
Lab Notebook Cell Culture
PEI transfection of HEK cells
- Split the cells 1:5 into 10 cm plate (on 21.04.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 1 ml serum free DMEM (2.5µg from each plasmid)
- Add 15 µl PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add the mix to the culture
13.05.17
PEI transfection of HEK, Jurkat, HPB-ALL and HUT78 cells
- Split cells 1:5 to a 6-well plate: 100 µl/well (on 12.05.17)
- For each sample: 3 µg plasmid DNA + 200 µl serum free DMEM
- Establish Mastermix
- Add 9 µg PEI to each mix while vortexing (PEI:DNA=3:1)
- 15 min incubation
- Add the Mix to the cells: 275.25 µl GFP-Mix or 215.5 µl to corresponding samples
- After 48h: Fluorescence Microscopy
Plasmid number | component | concentration[ng/µL] | volume[µL] for 12 µg |
---|---|---|---|
pIG17_008 | CMV_mCherry-delta-PstI_pA | 471.5 | 25 |
pIG17_009 | CMV_EGFP_pA | 368.4 | 30 |
23.05.17
PEI transfection of HEK, Jurkat, HPB-ALL and HUT78 cells
Plasmid number | component |
---|---|
pIG17_008 | CMV_mCherry-delta-PstI_pA |
pIG17_009 | CMV_EGFP_pA |
- Split cells 1:5 to a 6-well plate: 330 µl (from 10 cm plate)/well (22.05.17)
- For each sample: 3 µg plasmid DNA + 200 µl serum free DMEM
- Establish Mastermix
- Add PEI to each mix while vortexing (PEI:DNA=3:1)
- 15 min incubation
- Add the Mix to the cells
- After 48h: Fluorescence Microscopy & Flow Cytometry
Lipotransfection of Jurkat, HPB-ALL and HUT78 cells
Plasmid number | component |
---|---|
pIG17_009 | CMV_EGFP_pA |
- pGFP: 2.5 µg/well
- Mix I: 150 µl serum free DMEM and 6 µl LTX reagent
- Mix II: 700 µl SERUM FREE DMEM + 2.5 µg pGFP + 14 µl PLUS reagent
- Mix 150 µl Mix I with 150 µl Mix II
- 5 min incubation at RT
- Add 300 µl to cells
30.05.17
BioRad electroporation
Cell lines: HPB-ALL, HUT78 and Jurkat Plasmid: pIG17_009 (GFP plasmid)
- Count the cells
- Transfer 1 mio. cells into falcons and centrifuge with 100g for 3 min
- Resuspend the cell pellet with 100 µl P3 Buffer
- Add 3 µg pIG17_009
- Transfer the mixture into cuvette
- BioRad setting: 250 V, 960 µF, 35 sec.
- Add 500 µl RPMI medium to the cells immediately after electroporation
- Plate the cells into 12-well plate with 2 ml Medium
- Over night culturing
- Wash the cuvettes for reusing
preparation for lentiviral transduction
Plate 4 mio. Hek cells in 10 cm plate. (Will be around 7-8 mio cell the next day)
(optional: 5-6 mio. Hek cells in 15 cm plate)
06.06.17
Production of Lentivirus
Transfection of HEK cells for virus production.
Lentiviral packaging cells | Hek293T cells |
Plate size | 10 cm |
Total DNA/plate | 12.87 µg |
Transfer: gag/pol: env ratio | 2:1:1 |
Construct | 6.43 µg |
pCMV∆R8.74 | 3.22 µg |
pMD2G | 3.22 µg |
N/P ration | 15 |
Plasmid number | component | concentration[ng/µL] | volume [µL] |
---|---|---|---|
pIG17_082 | Transfer plasmid with GFP p526 | 253 | 25.4 |
pIG17_003 | Envelope plasmid pMD2G | 105 | 30.7 |
pIG17_004 | Packaging Plasmid pCMV∆R8.74 | 150 | 21.5 |
- Packaging Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
pIG17_003 | 30.63 | 45.03 |
pIG17_004 | 21.44 | 64.33 |
150mM NaCl | 441.49 | 927.12 |
total | 493.56 | 1036.476 |
- PEI Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
23.2mM (1 µg/µl)PEI | 24.94 | 52.41 |
150mM NaCl | 475.04 | 997.59 |
total | 499.98 | 1050 |
07.06.17
Amaxa electroporation
Cell lines: HUT78 and Jurkat Plasmid: pIG17_008 (mCherry plasmid)
- Count the cells
- Transfer 1 mio. cells into falcons and centrifuge with 100g for 3 min
- Resuspend the cell pellet with 100 µl P3 Buffer
- Add 3 µg pIG17_008
- Transfer the mixture into cuvette
- Amaxa Programm: X-005
- Add 500 µl RPMI medium to the cells immediately after electroporation
- Plate the cells into 12-well plate with 2 ml Medium
- Over night culturing
- Wash the cuvettes for reusing
Production of Lentivirus
- Collect the medium (containing virus supernatant) and add new medium after 24h
BioRad electroporation
Cell lines: HUT78 and Jurkat Plasmid: pIG17_009 (GFP plasmid)
- Count the cells
- Transfer 1 mio. cells into falcons and centrifuge with 100g for 3 min
- Resuspend the cell pellet with 100 µl P3 Buffer
- Add 3 µg pIG17_009
- Transfer the mixture into cuvette
- BioRad setting: 250 V, 960 µF, 35 sec.
- Add 500 µl RPMI medium to the cells immediately after electroporation
- Plate the cells into 12-well plate with 2 ml Medium
- Over night culturing
- Wash the cuvettes for reusing
08.06.17
Production of Lentivirus
- Collect the medium (containing virus supernatant) and add new medium after 48h
- Mix with medium collected after 24h
Flow Cytometry
- negative controls: Hut78 and Jurkat cells.
- positive control: GFP_Jurkat(p526)
- Amaxa Samples: Hut78 (mCherry and GFP) and Jurkat (mCherry)
- BioRad Samples: Hut78 (GFP) and Jurkat (GFP)
- Count the cells
- resuspend cell pellet (about 1 mio.) with FACS Buffer (PBS with 1%FCS)
09.06.17
Lentiviral transduction
- Plate about 200000 cells for each wells.
- Incubate the plates over weekend in incubator.
Jurkat sample | Medium [ml] | Virus [ml] |
---|---|---|
1 | 1 | 1 |
2 | 0 | 2 |
Hut78 sample | Medium [ml] | Virus [ml] |
---|---|---|
1 | 2 | 0 |
2 | 1.5 | 0.5 |
3 | 1 | 1 |
4 | 0 | 2 |
HEK sample | Medium [ml] | Virus [ml] |
---|---|---|
1 | 2 | 0 |
2 | 1.5 | 0.5 |
3 | 1 | 1 |
4 | 0 | 2 |
10.06.17
BioRad electroporation
- Cell lines: Hut78
- Plasmid: pIG17_008 (mCherry plasmid)
Component | Amount |
---|---|
Hut cells | 3 mio. cells |
pIG17_008 | 5 µg |
Setting | Capacitance[µF] | Voltage | Cuvette size[cm] | Time Constance [msec] |
---|---|---|---|---|
Setting 1 | 250 | 150 | 0.2 | 4.0 |
Setting 2 | 500 | 120 | 0.2 | 10.1 |
12.06.17
Lentiviral transduction
- After 72h → Change the medium of the plates (for suspension cells: first centrifuge and then resuspend cell pellet with new medium)
- Incubation over night for FACS
Flow Cytometry for BioRad electroporation on June 10th
no positive population
13.06.17
Flow Cytometry for lentiviral infected cells
with ration of 1:1 (Medium vs. Virus medium) cells were most frequently infected and viable.
BioRad Electroporation
- Cell lines: Jurkat & Hut78
- Plasmid: pIG17_009
- Cell count: 1 mio. (Jurkat) 4 mio. (Hut78)
- Settings:
Cell type | Setting | Capacitance[µF] | Voltage | resistence | Time Constance [msec] |
---|---|---|---|---|---|
Jurkat | Setting 1 | 300 | 250 | ∞ | 35 |
Jurkat | Setting 2 | 350 | 200 | 1000Ω | 35 |
Hut78 | Setting 1 | 250 | 150 | ∞ | 50 |
Hut78 | Setting 2 | 500 | 120 | ∞ | 50 |
14.06.17
Amaxa electroporation
- Cell lines: Jurkat & Hut78
- Plasmid: pIG17_009
- Cell count: 1 mio.
- Program: X-005
- Flow cytometry after 24h.
Flow Cytometry for BioRad electroporated JK cells
No positive cell population.
15.06.17
Flow Cytometry for BioRad electroporated Hut78 cells and Amaxa electroporated T cells
no positive cell population.
16.06.17
Mycoplasma test(lentiviral transduced Jurkat and Hut78)
- Jurkat(p526): mycoplasma positive
- Hut78(p526):mycoplasma positive
- HEK(p526): mycoplasma negative
No cell sorting, stock cultures should be sent for test.
17.06.17
BioRad Electroporation with JK cells
- Cell lines: Jurkat
- Plasmid: pIG17_009
- Cell count: 2 mio./ approach
- 4 approaches:
Approach | Capacitance[µF] | Voltage | Cuvette size[cm] | Time Constance [msec] |
---|---|---|---|---|
1:negative control | 960 | 250 | 0.2 | 35 |
2:condition 1 | 960 | 250 | 0.2 | 35 |
3:condition 2 | 960 | 250 | 0.2 | 35 |
4:condition 3 | 960 | 250 | 0.2 | 40 |
PEI transfection with HEK cells
4 approaches:
- 1 transfection with pIG17_009
- 2 transfections with pIG17_013
- 1 untransfected as control
- Split cells 1:5 to a 6-well plate: 100 µl/well (on 16.06.17)
- For each sample: 3 µg plasmid DNA + 200 µl serum free DMEM
- Establish Mastermix
- Add 9 µg PEI to each mix while vortexing (PEI:DNA=3:1)
- 15 min incubation
- Add the Mix to the cells
- After 48h: Fluorescence Microscopy & Flow cytometry
Plasmid number | component |
---|---|
pIG17_013 | pHRE_Ptal_EGFP_pA |
19.06.17
Hypoxia test (CoCl2)
- Cell: via PEI transfected HEK cells.
- CoCl2 stock: 1M
- End concentration of CoCl2: 100µM
- Cell observation under fluorescence microscopy after 2h:
-By adding CoCl2, the HRE-GFP transfected cells showed less fluorescence signal than without CoCl2…
- Flow cytometry: no expected signal
BioRad Electroporation
- Cell lines: Jurkat
- Plasmid: pIG17_009
- Cell count: 2 mio./ approach
- Setting: 96 well plates, well set 1(ABCD1)
- 4 approaches:
Approach | Capacitance[µF] | Voltage | Cuvette size[cm] | Time Constance [msec] |
---|---|---|---|---|
1:negative control | 960 | 250 | 0.2 | 35 |
2:condition1 | 960 | 250 | 0.2 | 35 |
3:condition2 | 960 | 250 | 0.2 | 30 |
4:condition3 | 960 | 250 | 0.2 | 40 |
20.06.17
BioRad electroporation
- Cell lines: Jurkat
- Plasmid: pIG17_009
- Cell count: 2 mio./ approach
- Setting: 96 well plates, well set 1(ABCD1), Expotential
- 4 approaches:
Approach | Capacitance[µF] | Voltage | Cuvette size[cm] | Resistance |
---|---|---|---|---|
1:negative control | 950 | 250 | 0.2 | 1000Ω |
2:condition1 | 350 | 250 | 0.2 | ∞ |
3:condition2 | 300 | 300 | 0.2 | 1000Ω |
4:condition3 | 300 | 250 | 0.2 | 1000Ω |
21.06.17
Mycoplasma-Test (Stock cultures)
- HEK293T: mycoplasma negative
- Jurkat: mycoplasma negative
- Hut78: mycoplasma positive → abort culturing of Hut78!
Flow Cytometry (BioRad on Jun.19th)
- Not successful
24.06.17
PEI transfection (pIG17_013) for hypoxia test
- In total: 3*6 wells
- Transfection with pIG17_009 as positive control: 1 well/plate
- Transfection with pIG17_013: 4 well/plate
- Split the cells 1:5 into 10 cm plate (on 23.06.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 1 ml serum free DMEM (3µg from each plasmid)
- Add 15 µl PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add 200µl mix to wells
25.06.17
Hypoxia test (CoCl2)
- Cell: 1 plate of via PEI transfected HEK cells. (from 24.06)
- CoCl2 stock: 1M
- End concentration of CoCl2: 100µM
Well | End concentration of CoCl2[µM] | Volume of Stock CoCl2[µl] |
---|---|---|
1: untransfected | 100 | 200 |
2:pIG17_009 transfected | - | - |
3:pIG17_013 transfected | - | - |
4:pIG17_013 transfected | 50 | 100 |
5:pIG17_013 transfected | 100 | 200 |
6:pIG17_013 transfected | 200 | 400 |
* Cell observation under fluorescence microscopy every hour after CoCl2 treatment
- Flow cytometry after 8 hours
BioRad Electroporation
- Cell lines: Jurkat
- Plasmid: pIG17_009
- Cell count: 2 mio./ approach
- Setting: 12 well plates, well set 1
- 3 approaches:
Approach | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|
1:3 µg plasmid | 960 | 250 | ∞ | 20 |
2:6 µg plasmid | 960 | 250 | ∞ | 20 |
3:9 µg plasmid | 960 | 250 | ∞ | 20 |
- Flow cytometry after 24h.
26.06.17
Hypoxia test (CoCl2)
1.Plate
Duration of Treatment | Well | End concentration of CoCl2[µM] | Volume of Stock CoCl2[µl] |
---|---|---|---|
6h | 1: untransfected | 100 | 200 |
6h | 2:pIG17_009 transfected | - | - |
6h | 3:pIG17_013 transfected | - | - |
6h | 4:pIG17_013 transfected | 50 | 100 |
6h | 5:pIG17_013 transfected | 100 | 200 |
6h | 6:pIG17_013 transfected | 200 | 400 |
2.Plate
Duration of Treatment | Well | End concentration of CoCl2[µM] | Volume of Stock CoCl2[µl] |
---|---|---|---|
24h | 1: untransfected | 100 | 200 |
24h | 2:pIG17_009 transfected | - | - |
24h | 3:pIG17_013 transfected | - | - |
24h | 4:pIG17_013 transfected | 50 | 100 |
24h | 5:pIG17_013 transfected | 100 | 200 |
24h | 6:pIG17_013 transfected | 200 | 400 |
Flow Cytometry (Hypoxia test & BioRad)
Hypoxia test
No induction of GFP expression under hypoxia condition Problems:
- Cells stayed attached to the ground of plates even after treating with trypsin
- Cells clumps instead of single cell were detected
BioRad Electroporation
By increasing the amount of plasmid DNA, some cells were potentially transfected!!!
27.06.17
BioRad Electroporation
9µg for each approach
- Setting: 12 well plate, 1 well set, 1 pulse
GFP Plasmid: pIG17_009
Approach | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|
1 | 950 | 250 | ∞ | 20 |
2 | 950 | 250 | 1000Ω | 20 |
3 | 950 | 250 | 1500Ω | 20 |
Knock out
Approach | Plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | 203 (Cas9) + 104 (gRNA) | 950 | 250 | ∞ | 20 |
2 | 203 (Cas9)+ scramble | 950 | 250 | ∞ | 20 |
3 | sgRNA3 (gRNA_GFP) | 950 | 250 | ∞ | 20 |
4 | sgRNA3 (gRNA_GFP) | 950 | 250 | ∞ | 20 |
28.06.17
Flow Cytometry: electroporation on June 27th
29.06.17
Production of Lentivirus
Transfection of HEK cells for virus production.
Lentiviral packaging cells | Hek293T cells |
Plate size | 10 cm |
Total DNA/plate | 12.87 µg |
Transfer: gag/pol: env ratio | 2:1:1 |
Construct | 6.43 µg |
pCMV∆R8.74 | 3.22 µg |
pMD2G | 3.22 µg |
N/P ration | 15 |
Plasmid number | component | concentration[ng/µL] | volume [µL] |
---|---|---|---|
pIG17_? | LentiCRISPR(AG Cathomen) | 1100 | 5.85 |
pIG17_003 | Envelope plasmid pMD2G | 68 | 47.4 |
pIG17_004 | Packaging Plasmid pCMV∆R8.74 | 209 | 15.4 |
- Packaging Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
pIG17_003 | 47.4 | 99.54 |
pIG17_004 | 15.4 | 32.34 |
150mM NaCl | 441.49 | 927.12 |
total | 504.3 | 1059 |
- PEI Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
23.2mM (1µg/µl)PEI | 24.94 | 52.41 |
150mM NaCl | 475.04 | 997.59 |
total | 499.98 | 1050 |
30.06.17
Production of Lentivirus
- Collect the medium (containing virus supernatant) and add new medium after 24h
01.07.17
Production of Lentivirus
- Collect the medium (containing virus supernatant) and add new medium after 24h
- Mix the virus medium (24h + 48h)
Lentiviral transduction
- Plate about 200000 cells for each wells.
- Incubate the plates over weekend in incubator.
Jurkat sample | Medium [ml] | Virus [ml] |
---|---|---|
1 | 2 | 0 |
2 | 1.5 | 0.5 |
3 | 1 | 1 |
4 | 0.5 | 1.5 |
5 | 0 | 2 |
PEI transfection with HEK for Hypoxia Test
- Prepare 2*6-well Plates of HEK cells
- Transfect cells via PEI:
well | plasmid |
---|---|
1 | - |
2 | pIG17_009 |
3 | pIG17_013 |
4 | pIG17_013 |
5 | pIG17_013 |
6 | pIG17_013 |
BioRad Electroporation: Repeat pGFP transfection
9µg for each approach
- Setting: 12 well plate, 1 well set, 1 pulse
Approach | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|
1: no plasmid | 950 | 250 | ∞ | 20 |
2: Mock plasmid | 950 | 250 | ∞ | 20 |
3: pIG17_009 | 950 | 250 | ∞ | 20 |
4: pIG17_009 | 950 | 250 | 1000Ω | 20 |
5: pIG17_009 | 950 | 250 | 1500Ω | 20 |
02.07.17
CoCl2 treatment with Jurkat cells
- Cells treated with CoCl2 built clumps, which depends on the incubation time and CoCl2 concentrations.
Repeat Hypoxia test (24h after PEI)
No induction of GFP expression under hypoxia condition
- Add different concentrations of CoCl2 (50µM, 100µM and 200 µM)
- Observe the cells under fluorescence microscope 3h, 6h, 8h, 16h, 18h and 24h after CoCl2 treatment
- No detectable induction of gene expression for every approach
Flow Cytometry (BioRad on July 1st)
- Both negative and positive controls showed abnormal populations → need to repeat the experiments.
03.07.17
Repeat Hypoxia test (48h after PEI)
No induction of GFP expression under hypoxia condition
- Add different concentrations of CoCl2 (50µM, 100µM and 200 µM)
- Observe the cells under fluorescence microscope 3h, 6h, 8h, 16h, 18h and 24h after CoCl2 treatment
- No detectable induction of gene expression for every approach
04.07.17
Lentiviral transduction (pLenti-CRISPR from AG Cathomen)
- Change the medium and add puromycin for selection
BioRad Electroporation: Repeat pGFP transfection
9µg for each approach
- Setting: 12 well plate, 1 well set, 1 pulse
Approach | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|
1: no plasmid | 950 | 250 | ∞ | 20 |
2: Mock plasmid | 950 | 250 | ∞ | 20 |
3: pIG17_009 | 950 | 250 | ∞ | 20 |
4: pIG17_009 | 950 | 250 | 500Ω | 20 |
5: pIG17_082 (p526) | 950 | 250 | ∞ | 20 |
05.07.17
PEI transfection (pIG17_022 and pIG17_023) for CTLA-4 promoter test
- In total: 3*6 wells
- Transfection with pIG17_009 as positive control: 1 well
- Transfection with pIG17_022: 4 wellS
- Transfection with pIG17_023: 4 wellS
- Per Approach: 3µg DNA, 200µl serum free DMEM and 9µg PEI
- Split the cells 1:5 into 10 cm plate (on 03.07.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 200µl serum free DMEM (3µg from each plasmid)
- Add PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add 200µl mix to wells
Flow Cytometry
- Cells transfected with pIG17_082 showed high transfection efficiency
- Cells transfected with our stock pIG17_009 showed low efficiency and low survival rate
06.07.17
Prepare cells for lentivirus-production
- Plate about 4 mio. cells, make replicate
VEGF induction with Modeling group
- No significant induction
07.07.17
Lentivirus(pIG17_119) production in HEK cells
Transfection of HEK cells for virus production.
Lentiviral packaging cells | Hek293T cells |
Plate size | 10 cm |
Total DNA/plate | 12.87 µg |
Transfer: gag/pol: env ratio | 2:1:1 |
Construct | 6.43 µg |
pCMV∆R8.74 | 3.22 µg |
pMD2G | 3.22 µg |
N/P ration | 15 |
Plasmid number | component | concentration[ng/µL] | volume [µL] |
---|---|---|---|
pIG17_119 | pCRE_GFP_CMV_mCherry | 167 | 38.5 |
pIG17_003 | Envelope plasmid pMD2G | 243.4 | 13.3 |
pIG17_004 | Packaging Plasmid pCMV∆R8.74 | 819 | 4 |
- Packaging Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
pIG17_003 | 13.3 | 28 |
pIG17_004 | 4 | 8.4 |
150mM NaCl | 441.49 | 927.12 |
total | 458.8 | 963.52 |
- PEI Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
23.2mM (1µg/µl)PEI | 24.94 | 52.41 |
150mM NaCl | 475.04 | 997.59 |
total | 499.98 | 1050 |
08.07.17
Lentivirus(pIG17_119) production in HEK cells
- Change the medium
BioRad electroporation
4 Approaches (9µg/Approach) Setting: 12 well plate, 1 well set, 1 Pulse, ∞ Resistance
- Electroporated without plasmid
- CMV-GFP from Nicole (700 ng/µl)
- CMV-GFP (Yael, 06.06.17, 140.4 ng/µl)
- CMV-GFP (Dennis, 27.06.17, Dennis, 86.8 ng/µl)
09.07.17
Lentivirus(pIG17_119) production in HEK cells
- Collect virus medium
- Add new medium
10.07.17
Lentivirus(pIG17_119) production in HEK cells
- Collect virus medium
- Add new medium
11.07.17
PEI transfection (CTLA-4 Test)
- In total: 3*6 wells
- Transfection with pIG17_009 as positive control: 1 well (plasmid from Nicole); 1 well (Culture from Nicole, from us preped using promega miniprep)
- Transfection with pIG17_022: 5 wellS
- Transfection with pIG17_023: 5 wellS
- Per Approach: 3µg DNA, 200µl serum free DMEM and 9µg PEI
- Split the cells 1:5 into 10 cm plate (on 03.07.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 200µl serum free DMEM (3µg from each plasmid)
- Add PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add 200µl mix to wells
Lentiviral transduction (pIG17_119) of Jurkat cells
- Use 6-well plate
- plate 200000 cells/well
- Make Titer test with virus medium
The cells were not successfully infected.
12.07.17
BioRad electroporation
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | no plasmid | 950 | 250 | ∞ | 20 |
2 | CMV-GFP (Nicole) | 950 | 250 | ∞ | 20 |
3 | CMV-GFP (Culture from Nicole, promega mini) | 950 | 250 | ∞ | 20 |
4 | pIG17_104: Cas9-GFP-gRNA3 | 950 | 250 | ∞ | 20 |
14.07.17
Lentivirus(pIG17_121) production in HEK cells
Transfection of HEK cells for virus production.
Lentiviral packaging cells | Hek293T cells |
Plate size | 10 cm |
Total DNA/plate | 12.87 µg |
Transfer: gag/pol: env ratio | 2:1:1 |
Construct | 6.43 µg |
pCMV∆R8.74 | 3.22 µg |
pMD2G | 3.22 µg |
N/P ration | 15 |
Plasmid number | component | concentration[ng/µL] | volume [µL] |
---|---|---|---|
pIG17_121 | pCTLA4(380)_GFP_CMV_mCherry | 1682 | 3.82 |
pIG17_003 | Envelope plasmid pMD2G | 321.9 | 10 |
pIG17_004 | Packaging Plasmid pCMV∆R8.74 | 819 | 4 |
- Packaging Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
pIG17_003 | 10 | 21 |
pIG17_004 | 4 | 8.4 |
150mM NaCl | 441.49 | 927.12 |
pIG17_121 | 3.82 | 8 |
total | 504.95 | 1060 |
- PEI Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
23.2mM (1µg/µl)PEI | 24.94 | 52.41 |
150mM NaCl | 475.04 | 997.59 |
total | 499.98 | 1050 |
BioRad electroporation
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | no plasmid | 950 | 250 | ∞ | 20 |
2 | 6µg Cas9-GFP-gRNA3 | 950 | 250 | ∞ | 20 |
3 | 9µg Cas9-GFP-gRNA3 | 950 | 250 | ∞ | 20 |
4 | 12µg Cas9-GFP-gRNA3 | 950 | 250 | ∞ | 20 |
15.07.17
collect virus (pIG17_121)
flow cytometry (BioRad 7/14)
16.07.17
PEI transfection
- In total: 3*6 wells
- One well with non-transfected cells
- Transfection with CMV-GFP as positive control: 1 well (JetStar); 1 well (Promega Mini)
- Transfection with pIG17_013: 4 wellS
- Per Approach: 3µg DNA, 200µl serum free DMEM and 9µg PEI
- Split the cells 1:5 into 6-well plate (on 15.07.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 200µl serum free DMEM (3µg from each plasmid)
- Add PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add 200µl mix to wells
BioRad electroporation
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | no plasmid | 950 | 250 | ∞ | 20 |
2 | CMV-GFP JetStar | 950 | 250 | ∞ | 20 |
3 | CMV-GFP promega mini | 950 | 250 | ∞ | 20 |
4 | CMV-mCherry (Nicole) | 950 | 250 | ∞ | 20 |
5 | pIG17_008 (Jana) | 950 | 250 | ∞ | 20 |
17.07.17
Hypoxia Test in hypoxia incubator (AG Cathomen)
- with 1%O2
Flow Cytometry
- BioRad didn't work
18.07.17
Hypoxia Test in hypoxia incubator (AG Cathomen)
- Fluorescence microscopy
- After 24h incubation: cells showed normal morphology and there was no autofluorescence.
Lentiviral transduction
- wash the virus-transducted cells (pIG17_119)
BioRad electroporation
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | pIG17_119 | 950 | 250 | ∞ | 20 |
2 | pIG17_121 | 950 | 250 | ∞ | 20 |
3 | pIG17_031 | 950 | 250 | ∞ | 20 |
4 | pIG17_034 | 950 | 250 | ∞ | 20 |
5 | pIG17_037 | 950 | 250 | ∞ | 20 |
5 | pIG17_086 | 950 | 250 | ∞ | 20 |
PEI transfection (CTLA-4 Test)
- In total: 2*12 wells
- One well with non-transfected cells
- One well: Transfection with CMV-GFP as positive control
- Transfection with pIG17_022: 5 wellS
- Transfection with pIG17_023: 5 wellS
- Transfection with pIG17_037: 5 wellS
- Transfection with pIG17_086: 5 wellS
- Per Approach: 1.5µg DNA, 100µl serum free DMEM and 4.5µg PEI
- Split the cells 1:10 into 12-well plate (on 17.07.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 100µl serum free DMEM (3µg from each plasmid)
- Add PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add 100 µl mix to wells
PEI transfection (hypoxia test with CoCl2)
- In total: 4*6-well plates
- One well in each plate: with non-transfected cells
- One well in each plate: Transfection with CMV-GFP as positive control
- Transfection with pIG17_013: 8 wellS
- Transfection with pIG17_031: 8 wellS
- Split the cells 1:10 into 6-well plate (on 17.07.17)
- Thaw PEI reagent at RT
- Dilute plasmid in 100µl serum free DMEM (3µg from each plasmid)
- Add PEI(1µg/µl) to the mix while vortexing (PEI:DNA=3:1)
- incubate 15 min at RT
- Add 200 µl mix to wells
19.07.17
Concentrate the viruses (pIG17_119 and pIG17_121)
- for 20 ml virus medium, use 5ml 20% sucrose
- carefully add virus medium to sucrose (very tricky)
- centrifuge at 4000 rpm over night
- After centrifugation: remove the medium, put the falcon tube upside down and air dry.
- slowly add 100 µl PBS (20-30x, also very tricky)
- Incubate the pellet for 30-60 min
- resuspend the cells 2x
- aliquot the virus
- store in -80°C freezer
Lentiviral transduction
- plate 200000 Jurkat cells/ well in one 6-well plate
- add the concentrated virus (pIG17_119 and pIG17_121) (30µl and 50µl)
CoCl2 treatment (24h after PEI)
- Treatment with 2*6 well plate: 1 with pIG17_013 and 1 with pIG17_031
- Make new 2M CoCl2 stock
- add CoCl2 to the cells, end-concentration: 0, 300µM, 500µM and 100µM
- Incubation for 24h and track the induction of cell expression
Hypoxia Test in hypoxia incubator (AG Cathomen)
- Fluorescence microscopy
- After 48h incubation: cells were mostly dead showing autofluorescence.
Flow Cytometry (BioRad on July 20th)
- For mCherry excitation: FL3!!!
20.07.17
CoCl2 treatment (48h after PEI)
- Treatment with 2*6 well plate: 1 with pIG17_013 and 1 with pIG17_031
- Make new 2M CoCl2 stock
- add CoCl2 to the cells, end-concentration: 0, 300µM, 500µM and 100µM
- Incubation for 24h and track the induction of cell expression
Hypoxia Test in hypoxia incubator (AG Cathomen)
- Fluorescence microscopy
- After 72h incubation: cells were mostly dead showing autofluorescence.
21.07.17
BioRad Electroporation (Knock-Out plasmids)
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | - | 950 | 250 | ∞ | 20 |
2 | CMV-GFP (#503 from Nicole) | 950 | 250 | ∞ | 20 |
3 | pIG17_082 (p526) | 950 | 250 | ∞ | 20 |
4 | Cas9-GFP-gRNA5 | 950 | 250 | ∞ | 20 |
5 | Cas9-GFP-scramble | 950 | 250 | ∞ | 20 |
22.07.17
Lentivirus(pIG17_119 and pIG17_121) production in HEK cells
PEI Transfection of HEK cells for virus production.
Lentiviral packaging cells | Hek293T cells |
Plate size | 10 cm |
Total DNA/plate | 12.87 µg |
Transfer: gag/pol: env ratio | 2:1:1 |
Construct | 6.43 µg |
pCMV∆R8.74 | 3.22 µg |
pMD2G | 3.22 µg |
N/P ration | 15 |
Plasmid number | component | concentration[ng/µL] | volume [µL] |
---|---|---|---|
pIG17_119 | pCRE_GFP_CMV_mCherry | 167 | 38 |
pIG17_121 | pCTLA4(380)_GFP_CMV_mCherry | 1682 | 3.82 |
pIG17_003 | Envelope plasmid pMD2G | 105 | 30.7 |
pIG17_004 | Packaging Plasmid pCMV∆R8.74 | 208 | 15.5 |
- Packaging Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
pIG17_003 | 30.7 | 64.5 |
pIG17_004 | 15.5 | 32.6 |
150mM NaCl | 441.49 | 927.12 |
- PEI Mastermix
Component | 1x [µL] | 2.1x [µL] |
---|---|---|
23.2mM (1µg/µl)PEI | 24.94 | 52.41 |
150mM NaCl | 475.04 | 997.59 |
total | 499.98 | 1050 |
22.07.17
Flow Cytometry: BioRad Electroporation 7/21
there was GFP positive signals during flow cytometry measurement but the cells were mycoplasma positive
Lentivirus(pIG17_119 and pIG17_121) production in HEK cells
- Collect virus
23.07.17
Lentivirus(pIG17_119 and pIG17_121) production in HEK cells
- Collect virus
24.07.17
Mycoplamsa Test
- Both Cas9-GFP-gRNA5 and Cas9-GFP-scramble transfected cells were mycoplasma positive
25.07.17
PEI transfection of CHO cells: Hypoxia & Tet system
- Split the cells 1:2 in 12-well plate (on 24.07.17)
- Per Approach: 1µg DNA + 8µg PEI and fill up to 100 µl with serum free DMEM
- Thaw PEI reagent at RT
- Add PEI(1µg/µl) to the mix while vortexing
- incubate 15 min at RT
- Add the mix to cells
Plasmid | Approach | DNA Concentration[ng/µl] | DNA volume | Volume of DMEM[µl] |
---|---|---|---|---|
CMV-GFP (#503 from Nicole) | 1 | 25.5 | 40 | 52 |
CMV-mCherry (AG Hiltbrunner) | 1 | 1200 | 1 | 91 |
pIG17_012 | 6 | 253 | 24 | 528 |
pIG17_013 | 6 | 583.3 | 10.3 | 541.7 |
pIG17_031 | 6 | 746.9 | 8 | 544 |
Tet-GFP (Shima) | 2 (protocol from Shima) | 520 | 3.8 | 180.2 |
Tet-GFP (Shima) | 2 (our protocol) | 520 | 5.8 | 200 |
Tetracycline induction of CHO
- 3h after PEI transfection: remove media, add tetracycline to new media (1:1000 dilution)
- Tetracycline Stock: 2mg/ml (End: 1µg per well of 12-well plate)
- 3h after adding tetracycline: no induction
- incubation till the next day: microscopic observation
- Gene expression was induced by tetracycline compared to the tetracycline-untreated cells
PEI transfection of HEK cells: Hypoxia
- Split the cells 1:5 in 12-well plate (on 24.07.17)
- Per Approach: 1.5µg DNA + 4.5µg PEI and 100 µl serum free DMEM
- Thaw PEI reagent at RT
- Add PEI(1µg/µl) to the mix while vortexing
- incubate 15 min at RT
- Add the mix to cells
Plasmid | Approach | DNA Concentration[ng/µl] | DNA volume |
---|---|---|---|
CMV-GFP (#503 from Nicole) | 1 | 25.5 | 59 |
CMV-mCherry (AG Hiltbrunner) | 1 | 1200 | 1.25 |
pIG17_012 | 6 | 131.4 | 12 |
pIG17_013 | 6 | 583.3 | 15.5 |
pIG17_031 | 6 | 746.9 | 12 |
26.07.17
CoCl2 treatment
- Add corresponding concentration of CoCl2 to (hypoxic plasmid) transfected cells (CHO and HEK)
- CoCl2 stock: 2M
Endconcentration of CoCl2[µM] | Volume from Stock[µl] |
---|---|
0 | 0 |
100 | 0.1 |
200 | 0.2 |
300 | 0.3 |
500 | 0.5 |
1000 | 1 |
27.07.17
SEAP assay with HEK cells
- gather 200 µl of cell supernatant
- incubate cell supernatant at 65°C for 30min
- centrifuge cell supernatant for 1 min at 1250g
- add 150 µl supernatant into a cuvette
- add 500 µl 2x SEAP buffer
- add 100 µl pNPP and remove bubbles carefully
- measure in a nano drop every 5min for 2h
Replace Stock cultures with new culture from Toolbox
31.07.17
Mycoplasma Test: New HEK stock
- New HEK cells were mycoplasma negative
01.08.17
BioRad Electroporation
- Per Approach: 9µg DNA, 2 mio.JK cells
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | pIG17_009 (06.06 Yael) | 950 | 250 | ∞ | 20 |
2 | Cas9-GFP-gRNA5 | 950 | 250 | ∞ | 20 |
3 | Cas9-GFP-scramble | 950 | 250 | ∞ | 20 |
4 | KO-Kit: 203+101 | 950 | 250 | ∞ | 20 |
5 | KO-Kit: 203+104 | 950 | 250 | ∞ | 20 |
6 | KO-Kit scramble | 950 | 250 | ∞ | 20 |
PEI transfection: Hypoxia - SEAP assay in HEK cells
- Per Approach: 1.5µg DNA, 4.5µg PEI, 100µl DMEM
Plasmid number | component | concentrations of the used tubes[ng/µL] | volumes from the used tubes[µL] for 36µg |
---|---|---|---|
pIG17_013 | HRE-SEAP | 583.3 and 88.1 | 55.7 and 40 |
pIG17_002 | CMV-SEAP | 92.0 and 91.4 | 350 and 41.6 |
Due to the concentrations and volumes in the tubes for each approach two were used. Per construct 24 wells were used. Each well will have different CoCl2 concentrations. For each approach triplicates will be analysed.
02.08.17
Flow Cytometry of BioRad Electroporation (8/1): KO plasmids
For the knockout Kit we could see the most living GFP positive cells (26.2%) for the cotransfection of 203 and 104. The Cas9 GFP guide RNA5 had 5.21% GFP positive cells under the gated living cells.
Addition of CoCl2: Hypoxia - SEAP assay in HEK cells
1:10 dilution of a 2M CoCl2 stock with PBS. CoCl2 was added to HRE-SEAP approaches in order to induce the promoter, as well as to CMV-SEAP approaches
Approaches: For each approach triplicates were done.
CoCL2 concentration[µM] | volume[µL] of 200mM CoCl2 |
---|---|
0 | 0 |
100 | 0.55 |
150 | 0.825 |
200 | 1.1 |
250 | 1.375 |
300 | 1.65 |
500 | 2.75 |
1000 | 5.5 |
Lentivirus production in HEK cells: Mock, Knock-down plasmid (114,115,116), pIG17_119, pIG17_121
Follow the protocol from Frederike (AG Schamel) PEI Transfection of HEK cells for virus production.
- Prepare packaging and PEI mix separately and incubate for 10 min
- Mix packaging mix with transferplasmid
- Add PEI mix to DNA mix and incubate for 15 min
- Add the PEI+DNA mix to cells
Lentiviral packaging cells | Hek293T cells |
Plate size | 10 cm |
Total DNA/plate | 12.87 µg |
Transfer: gag/pol: env ratio | 2:1:1 |
Construct | 6.43 µg |
pCMV∆R8.74 | 3.22 µg |
pMD2G | 3.22 µg |
N/P ration | 15 |
Plasmid number | component | No. of Approaches | concentration[ng/µL] | volume [µL] |
---|---|---|---|---|
pIG17_082 | Mock(p526):EF1-GFP | 2 | 68 | 189.1 |
pIG17_114 | Knock-down plasmid | 2 | 350; 432 | 18.4; 15 |
pIG17_115 | Knock-down plasmid | 1 | - | all two tubes |
pIG17_116 | Knock-down plasmid | 2 | 492; 356 | 20; 8.5 |
pIG17_003 | Envelope plasmid pMD2G | 7 | 150;68.7;63.7 | 30;180;80 |
pIG17_004 | Packaging Plasmid pCMV∆R8.74 | 7 | 926.6 | 24.3 |
- Packaging Mastermix
Component | 7x [µL] |
---|---|
pIG17_003 | 290 |
pIG17_004 | 24.3 |
150mM NaCl | 3090.43 |
Follow our protocol of PEI transfection
- DNA:PEI ratio = 1:8
- Mix DNA with 1 ml serum free DMEM
- Add PEI while vortexing
- 15 min incubation
Component | Mass/approach[µg] |
---|---|
pIG17_003 | 3.2 |
pIG17_004 | 3.2 |
pIG17_119 | 6.4 |
pIG17_121 | 6.4 |
03.08.17
Hypoxia - SEAP assay in HEK cells
- gather 200 µl of cell supernatant
- incubate cell supernatant at 65°C for 30min
- centrifuge cell supernatant for 1 min at 1250g
- add 80 µl supernatant into a 96 well plate
- add 100 µl 2x SEAP buffer
- add 20 µl pNPP and remove bubbles carefully
- measure in the plate reader every 30s for 2h
–> Experiment failed and will be repeated
05.08.17
Lentiviral Transduction
- Plate 200000 Jurkat cells/well in 6-well plate
- Titer Test of virus
- Incubation during weekend
Puromycin killing curve
- testing of untransfected JK cells and the scramble JK cells that have been transfected with the KO Kit (for each 5 conditions will be tested)
- dilution of the Puro stock (10 mg/ml) 1:100 –> 100 µg/ml
- cells will be distributed in a 12 well plate with 1 ml of media
concentration of Puro | volume from 100 µg/ml [µl] |
---|---|
0 | 0 |
0.125 | 1.25 |
0.2 | 2 |
0.25 | 2.5 |
0.5 | 5 |
06.08.17
PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay
- cells will be distributed in a 12 well plate on the next day
- one master mix for PEI
- 1 ml DMEM, 30 µl PEI, 10 µg DNA per each approach
- cotransfection of CMV-SEAP (95%) and HRE-SEAP (95%) with CMV-GFP (5%)
construct | concentration [ng/µl] | volume added for 9.5 µg [µl] |
---|---|---|
HRE-SEAP | 248.2 | 38.3 |
CMV-SEAP | 415.2 | 22.9 |
construct | concentration [ng/µl] | volume added for 0.5 µg [µl] |
---|---|---|
CMV-GFP | 303.1 | 1.6 |
- Per Approach: 9µg DNA, 2 mio JK cells
BioRad Electroporation
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | no Plasmid | 950 | 250 | ∞ | 20 |
2 | CMV-GFP | 950 | 250 | ∞ | 20 |
3 | CMV-GFP | 950 | 250 | ∞ | 20 |
4 | Ca construct | 950 | 250 | ∞ | 20 |
5 | Ca construct | 950 | 250 | ∞ | 20 |
6 | Ca construct | 950 | 250 | ∞ | 20 |
7 | Cas9-GFP-gRNA1 | 950 | 250 | ∞ | 20 |
8 | Cas9-GFP-gRNA1 | 950 | 250 | ∞ | 20 |
9 | Cas9-GFP-gRNA4 | 950 | 250 | ∞ | 20 |
10 | Cas9-GFP-gRNA4 | 950 | 250 | ∞ | 20 |
11 | Cas9-GFP-gRNA5 | 950 | 250 | ∞ | 20 |
12 | Cas9-GFP-gRNA5 | 950 | 250 | ∞ | 20 |
13 | Cas9-GFP-scramble | 950 | 250 | ∞ | 20 |
14 | Cas9-GFP-scramble | 950 | 250 | ∞ | 20 |
07.08.17
PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay
- GFP was observed under the microscope
- the cells were evenly distributed onto 12 well plates
- induction with CoCl2 after the cells recovered from the transfer
- 8 conditions per approach, everything done in triplicates
concentration of CoCl2 [µM] | volume added [µl] |
---|---|
0 | 0 |
100 | 0,5 |
150 | 0,75 |
200 | 1 |
250 | 1,25 |
300 | 1,5 |
500 | 2,5 |
1000 | 5 |
08.08.17
Lentivirus production in HEK cells: Mock, pIG17_133, pIG17_119, pIG17_121
PEI for HRE-SEAP and CMV-SEAP; repetition of the SEAP assay
The SEAP assay was negative. No changes in the OD for either CMV-SEAP or HRE-SEAP could be observed. Due to these troubles the next test will be postponed till all constructs have undergone another test digestion and sequencing.
10.08.17
Lentiviral transduction
- Virus: pIG17_082, pIG17_119, pIG17_121 and pIG17_133
- Plate 200000 virus for infection
- As control: HEK with 1:1 infection
Cell Sorting: KO-plasmid transfected cells
11.08.17
BioRad Electroporation
- 9µg DNA and 2 mio. cells/ approach
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | no Plasmid | 950 | 250 | ∞ | 20 |
2 | KO Kit 203+101 | 950 | 250 | ∞ | 20 |
3 | KO Kit 203+104 | 950 | 250 | ∞ | 20 |
4 | Lenti-Cas9-Puro | 950 | 250 | ∞ | 20 |
Puromycin killing curve
Day 6 after addition of puromycin: due to low cell numbers, the cells were spun down, resuspended in 100 µl and then counted.
Results for untransfected Jurkat cells and Jurkat cells transfected with the scramble:
Puromycin addition to the electroplated KO Kit cells
Approaches:
- 1x scramble no treatment
- 1x scramble 0.2 µg/ml
- 2x KO Kit 203+101 0.2 µg
- 2x KO Kit 203+104 0.2 µg
Transfer to a 6 well plate
12.08.17
Puromycin: electroplated KO Kit cells
Due to low cell counts the duplicates were pooled together and the cells transferred to a 12 well plate.
14.08.17
PEI: HRE-SEAP, pWW56
in 10cm plates:
- 10 µg DNA
- 1ml DMEM
- 30 µl PEI
approaches:
- HRE-SEAP
- pWW56 as a positive SEAP control
- untransfected control
construct | concentration [ng/µl] | volume used for 10 µg DNA |
---|---|---|
HRE-SEAP | 420,5 | 23,78 |
pWW56 | 555,5 | 18,00 |
15.08.17
SEAP
- the cells were evenly distributed onto 12 well plates
- induction with CoCl2 after the cells recovered from the transfer
- 8 conditions per approach, everything done in triplicates
concentration of CoCl2 [µM] | volume added [µl] |
---|---|
0 | 0 |
100 | 0,5 |
150 | 0,75 |
200 | 1 |
250 | 1,25 |
300 | 1,5 |
500 | 2,5 |
1000 | 5 |
Electroporated KO Kit cells
Due to low cell counts the samples were transferred to a conical 96-well plate
BioRad Electroporation
Approach | plasmid | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|
1 | no Plasmid | 950 | 250 | ∞ | 20 |
2 | CMV-GFP + CMV-mCherry | 950 | 250 | ∞ | 20 |
3 | pIG17_086 | 950 | 250 | ∞ | 20 |
4 | pIG17_086 | 950 | 250 | ∞ | 20 |
Lentivirus Production in HEK cells
- Approached by Frederike (AG Schamel)
- 2 Approaches (pIG17_119 & pIG17_121) with our HEK cells, envelope & packaging plasmid,PEI
- 1 Approach (pIG17_119) with material from AG Schamel: HEK, envelope & packaging plasmid, PEI
16.08.17
SEAP
The SEAP assay was performed as mentioned before, however, there was a 1:5 dilution included of the HRE-SEAP samples.
For the analysis of the SEAP assay, the averages of the triplicates were calculated and the respective wild-type control subtracted from the HRE-SEAP samples.
For the undiluted HRE-SEAP construct the following graph was obtained:
For the 1:5 dilution the following graph was obtained:
For the 1:5 dilution absorbance values are missing at the start because they were negative and therefore regarded as 0.
The positive control did not work due to the promoter of this construct which was dependent on an input that wasn't given.
Furthermore, the samples did not show what we expected, considering that the uninduced control showed a steeper slope than most of the samples. Due to this reason the experiment was repeated.
17.08.17
Lentiviral Transduction with virus-medium
- Approaches for Titer test: both normal transduction and spin-infection.
- On 8/20: After washing the cells, there was no signal from reporter gene expression.
23.08.17
PEI transfection of HEK cells for lentivirus production
- Transferplasmid: pIG17_130 (duplicate)
25.08.17
Concentrate virus (pIG17_130)
- Add 8 ml 20% Sucrose (in PBS + 1Mm EDTA) in 50 ml Falcon Tube
- Add virus media slowly over sucrose (Use 25ml pippet)
- Centrifuge over night at 4000 rpm, 4°C
26.08.17
Lentiviral Transduction (pIG17_130)
- Plate 200000 cells/well (HEK & Jurkat) into 6 well plate
- Titer of virus: 0, 15 µl, 30 µl
As shown in the picture the transduction of HEK cells showed high efficiency. The cells were also mycoplasma-negative, so that the cells can be sorted at Bioss.
The efficiency of transduction was quite low. The positive signal showed above may come from dead cells. New transduction was done on 8/30 with higher virus titer (45µl and 60µl).
Lentiviral transduction of Jurkat cells with higher virus titer showed higher efficiency than previous try. These cells are sent for microplasma-test and for cell sorting.
30.08.17
PEI transfection of HEK cells for lentivirus production (133&134)
02.09.17
PEI transfection of HEK cells for lentivirus production (132)
04.09.17
BioRad Electroporation
9µg for each approach
- Setting: 12 well plate, 1 well set, 1 pulse
Number of approaches | Plasmid | Concentration [ng/µl] | Volume for 9ng [µl] | Capacitance[µF] | Voltage | Resistance | Time Constance [msec] |
---|---|---|---|---|---|---|---|
1 | no DNA | 0 | 0 | 950 | 250 | ∞ | 20 |
1 | CMV GFP, CMV mCherry | 327.1, 1200 | 1376, 3.75 | 950 | 250 | ∞ | 20 |
2 | pIG17_031 | 746.9 | 12.05 | 950 | 250 | ∞ | 20 |
2 | pIG17_034 | 1210.9 | 7.43 | 950 | 250 | ∞ | 20 |
2 | pIG17_037 | 851.9 | 10.56 | 950 | 250 | ∞ | 20 |
05.09.17
Washing of the electroporated cells
06.09.17
Sorting of the electroporated cells Gating after:
- living cells
- single cells
- mCherry positive cells
Sorting strategy:
Control igem_gfp_mcherry_jurkat_elektro_tube_001_06092017102918.pdf
pIG17_031 igem_gfp_mcherry_jurkat_31_tube_001_06092017103019.pdf
pIG17_034 igem_gfp_mcherry_jurkat_34_tube_001_06092017110102.pdf
pIG17_037 igem_gfp_mcherry_jurkat_37_tube_001_06092017112901.pdf
Sorting reports:
130 Jurkat: sort_report_06092017122940.pdf
pIG17_034 sort_report_06092017112206.pdf
pIG17_037 sort_report_06092017120252.pdf
07.09.17
Induction of the promoters
Set-up for pIG17_031 - hypoxia
- in a 96 well plate with 200 µl volume:
- used concentration of CoCl2: 20 mM
- approximately 15000 cells per approach
CoCl2 concentration [µM] | Number of approaches | Volume added [µl] |
---|---|---|
0 | 1 | 0 |
50 | 2 | 0.5 |
100 | 2 | 1 |
200 | 2 | 2 |
400 | 2 | 4 |
800 | 2 | 8 |
.
Set-up for pIG17_034 - pH
- in a 96 well plate with 200 µl volume:
- used concentration of NaOH: 1 M
- used concentration of lactate: 0.6 M
- used concentration of Forskolin: 10 mM
- approximately 15000 cells per approach
Lactate (L), NaOH (N) or Forskolin (F) concentration or pH | Number of approaches | Volume added [µl] |
---|---|---|
100 µM (F) | 1 | 2 |
8.17 pH (N) | 2 | 0.4 |
7.85 pH | 2 | 0 |
6.54 pH (L) | 2 | 8 |
6.19 pH (L) | 2 | 10.67 |
- 6 well plate with 3ml RPMI and the same concentration of lactate or NaOH as in the 96 well plate but without cells
- used in order to measure the pH
- amount of cells will be neglected as it is rather low
Set-up for pIG17_037 - VEGF
- in a 96 well plate with 200 µl volume:
- used concentration of VEGF: 1 µg/ml
- approximately 15000 cells per approach
VEGF concentration [ng/ml] | Number of approaches | Volume added [µl] |
---|---|---|
0 | 1 | 0 |
2.5 | 2 | 0.5 |
5 | 2 | 1 |
10 | 2 | 2 |
20 | 2 | 4 |
40 | 2 | 8 |
27.08.17 - 07.09.17
Neomycin killing curve of Jurkat cells
11.09.17
PEI transfection of HEK cells for lenvirus production
Viafect - new testing
Jurkat cells with CMV-GFP; transfection mix:
- 12 well plate
- 2 mio cells per well in 500 µl medium
- 0.5 µg DNA per well
- Viafect/DNA = 2:1 and 3:1
- 50 µl total volume per approach (filled up with serum free DMEM)
- removal of the medium from pelleted cells
- resuspending of pelleted cells in the transfection mix
- addition of 500 µl RPMI 1649 with FCS after
- 0 seconds
- 4 seconds
- 8 seconds
- 16 seconds
- 32 seconds
- transfer of the cell suspension to a 24 well plate
Analysis in the fluorescence microscope showed that this method did not work again
15.09.17
PEI transfection of HEK cells for lenvirus production
Constructs used: pIG17_130, CRE 4x
transfection_pei.pdf
20.09.17
PEI transfection of HEK cells for lenvirus production
Constructs used: NFAT 4x, HRE 4x
transfection_pei_20.9..pdf
The concentrated viruses were stored in -80°C freezer as backup.
21.09.17
PEI transfection of HEK cells for SEAP assay
The set up for the SEAP assay was the same as before, however there wild-type controls with the same amount of CoCl2 included.
All samples were done in triplicates
22.09.17
SEAP assay
Induction with CoCl2, the used concentrations of CoCl2 were: 0, 20, 40, 80, 160, 320 and 640 µM.
23.09.17
SEAP assay
The SEAP assay was performed as before, this time we included a cell count of each pooled triplicate.
For the analysis first the averages of the triplicates were calculated and then divided by the cell count. Afterwards, the corresponding wild-type control was subtracted from the samples and all negative values were set to 0.
We could see that only 20, 40 and 80 µM CoCl2 showed a steeper slope in our samples than the 0 µM control.
24.09.17
PEI transfection of HEK cells for lenvirus production
Constructs used: pIG17_134, CRE 4x
transfection_pei_lentivirus_24.9.17.xlsx
24.09.17
HRE testing with stable HEK cell lines
04.10.17
PEI transfection of HEK cells for lenvirus production
Constructs used: pIG17_133, Suiside plasmid transfection_pei_4.10.17.xlsx
09.10.17
CFP test
Due to the problems with our GFP readout we performed a search in BLAST and found out that our eGFP was wrongly annotate and is a eCFP. We also could see that in the FACS. For this we tested our Jurkat knockdown 130 cells, that stably express CFP then. On the left these cells are measured in the CFP channel and on the right in the GFP channel. The depicted cells are gated for living and single cells:
There is a clear shift and our cells are really CFP positive and not GFP positive
CRE Test in Jurkat cells
With Forskolin and IBMX, the cAMP pathway in the cell is activated.
- Cell lines: WT Jurkat, stable CRE4X Jurkat
- Conditions: untreated, induction with 100 µM Forskolin, induction with 100 µM IBMX, induction with 100 µM Forskolin and 100 µM IBMX.
FACS:
Cells were gated for living, single, mCherry positive cells and then the amount of CFP positive cells was measured:
10.10.17
HRE Test in Jurkat cells
HRE Test in HEK cells
12.10.17
CRE Test in HEK cells
- On 11th of Oct.: PEI transfection with CMV-TDAG8 plasmid.