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<div class="wrap-content"> | <div class="wrap-content"> | ||
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<h4 class="subtitle">Introduction</h4> | <h4 class="subtitle">Introduction</h4> | ||
<p class="text"> | <p class="text"> | ||
− | + | Several protocols for specific procedures have been followed while working in the wet lab. These include protocols for PCR, purifications, digestions, assemblies as well as working with Saccharomyces cerevisiae and Escherichia coli. See the exact procedures in the <a href="https://2017.igem.org/Team:Chalmers-Gothenburg/Notebook">lab journal</a>. | |
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− | + | ||
</p> | </p> | ||
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− | |||
<h4 class="sidetitle">Protocols</h4> | <h4 class="sidetitle">Protocols</h4> | ||
<h2> | <h2> | ||
− | + | Protocols for PCR | |
</h2> | </h2> | ||
+ | <div style="padding-left: 25px"> | ||
<p class="text"> | <p class="text"> | ||
− | <a href=""> | + | <a href="https://static.igem.org/mediawiki/2016/e/e9/T--Chalmers_Gothenburg--Protocols_DreamTaq_PCR.pdf">Thermo Scientific DreamTaq DNA Polymerase</a><br> |
− | <a href=""> | + | <a href="https://static.igem.org/mediawiki/2016/c/c9/T--Chalmers_Gothenburg--Protocols_Phusion_PCR.pdf">Thermo Scientific Phusion High-Fidelity DNA Polymerase</a><br> |
+ | <a href="https://static.igem.org/mediawiki/2016/a/a3/T--Chalmers_Gothenburg--Protocols_PrimeStar_PCR.pdf">PrimeSTAR HS DNA Polymerase</a><br> | ||
+ | <a href="">Fusion PCR</a> | ||
</p> | </p> | ||
− | + | </div> | |
<h2> | <h2> | ||
− | + | Protocols for purification | |
</h2> | </h2> | ||
+ | <div style="padding-left: 25px"> | ||
<p class="text"> | <p class="text"> | ||
− | <a href=""> | + | <a href="">Thermo Scientific GeneJET PCR Purification Kit</a><br> |
− | <a href=""> | + | <a href="">Thermo Scientific GeneJET Gel Extraction Kit</a> |
</p> | </p> | ||
+ | </div> | ||
<h2> | <h2> | ||
− | + | Protocols for digestion and assembly | |
</h2> | </h2> | ||
+ | <div style="padding-left: 25px"> | ||
<p class="text"> | <p class="text"> | ||
− | <a href=""> | + | <a href="">FastDigest Restriction Enzymes</a><br> |
− | <a href=""> | + | <a href="https://static.igem.org/mediawiki/2016/9/9d/T--Chalmers_Gothenburg--Protocols_gibson_assembly.pdf">Gibson Assembly Master Mix</a><br> |
+ | <a href="https://static.igem.org/mediawiki/2016/1/1d/T--Chalmers_Gothenburg--Protocols_general_DNA_insert_ligation.pdf">DNA Insert Ligation into Vector DNA</a> | ||
</p> | </p> | ||
+ | </div> | ||
− | + | <h2> | |
− | + | Protocols for <i>Saccharomyces cerevisiae</i> | |
− | + | </h2> | |
+ | <div style="padding-left: 25px"> | ||
+ | <p class="text"> | ||
+ | <a href="">Transformation (Chemical)</a><br> | ||
+ | <a href="https://static.igem.org/mediawiki/2016/d/de/T--Chalmers_Gothenburg--Protocols_S_cerevisiae_yeast_electroporation.pdf">Transformation (Electroporation)</a><br> | ||
+ | <a href="https://static.igem.org/mediawiki/2016/e/e2/T--Chalmers_Gothenburg--Protocols_S_cerevisiae_quick_genomic_extraction.pdf">Transformation (Quick version)</a><br> | ||
+ | <a href="https://static.igem.org/mediawiki/2016/9/98/T--Chalmers_Gothenburg--Protocols_S_cerevisiae_DNA_isolation_yeast.pdf">Isolation of genomic DNA</a> | ||
+ | </p> | ||
+ | </div> | ||
+ | |||
+ | <h2> | ||
+ | Protocols for <i>Escherichia coli</i> | ||
+ | </h2> | ||
+ | <div style="padding-left: 25px"> | ||
+ | <p class="text"> | ||
+ | <a href="https://static.igem.org/mediawiki/2016/f/f6/T--Chalmers_Gothenburg--Protocols_E_coli_transformation.pdf">Transformation (Heat shock)</a><br> | ||
+ | <a href="">Thermo Scientific GeneJET Plasmid Miniprep Kit</a> | ||
+ | </p> | ||
+ | </div> | ||
+ | |||
+ | <h2> | ||
+ | Protocols for Biobricks | ||
+ | </h2> | ||
+ | <div style="padding-left: 25px"> | ||
+ | <p class="text"> | ||
+ | <a href="https://static.igem.org/mediawiki/2016/c/c1/T--Chalmers_Gothenburg--Protocols_biobrick_assembly.pdf">BioBricks Assembly Protocol</a> | ||
+ | </p> | ||
+ | </div> | ||
+ | |||
+ | <h2> | ||
+ | Protocols for Interlab study | ||
+ | </h2> | ||
+ | <div style="padding-left: 25px"> | ||
+ | <p class="text"> | ||
+ | <a href="">Interlab study</a> | ||
+ | </p> | ||
+ | </div> | ||
+ | |||
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Revision as of 11:11, 17 October 2017
Notebook
Protocols
Introduction
Several protocols for specific procedures have been followed while working in the wet lab. These include protocols for PCR, purifications, digestions, assemblies as well as working with Saccharomyces cerevisiae and Escherichia coli. See the exact procedures in the lab journal.
Protocols
Protocols for PCR
Thermo Scientific DreamTaq DNA Polymerase
Thermo Scientific Phusion High-Fidelity DNA Polymerase
PrimeSTAR HS DNA Polymerase
Fusion PCR
Protocols for purification
Protocols for digestion and assembly
Protocols for Saccharomyces cerevisiae
Transformation (Chemical)
Transformation (Electroporation)
Transformation (Quick version)
Isolation of genomic DNA