Line 128: | Line 128: | ||
<ul><li>Christina</li></ul> | <ul><li>Christina</li></ul> | ||
</ul> | </ul> | ||
+ | </div> | ||
+ | |||
+ | <div id="date-7-10"> | ||
+ | <h1>Monday, July 10th.</h1> | ||
+ | <ul> | ||
+ | <li>InterLab Study:</li> | ||
+ | <ul> | ||
+ | <li>Christina, Felicia</li> | ||
+ | </ul> | ||
+ | <li>Dilution of several primers 1:10 (AD-RO Water µL45 , Primer µL5)</li> | ||
+ | <ul>Magdalena | ||
+ | </ul> | ||
+ | <li>PCR Gel Preparation</li> | ||
+ | <ul>Mathias | ||
+ | </ul> | ||
+ | </ul> | ||
+ | |||
+ | <div id="date-7-11"> | ||
+ | <h1>Tuesday, July 11th.</h1> | ||
+ | <ul> | ||
+ | <li>Planning & Fundraising</li> | ||
+ | <li>Golden Gate Assembly:</li> | ||
+ | <ul>Flpe (BB1), GFP (BB2) → Transformation (according to protocol) → Plating onto Agar (After Transformation): Selection with Ampicillin (bb1), Selection with Kanamycin(bb2), stored at 37°C over night | ||
+ | </ul> | ||
+ | <li>Dilution of several primer</li> | ||
+ | <ul><table class="table"> | ||
+ | <thead> | ||
+ | <tr> | ||
+ | <th>Abbreviation</th> | ||
+ | <th>Primer</th> | ||
+ | </tr> | ||
+ | </thead> | ||
+ | <tbody> | ||
+ | <tr> | ||
+ | <td>1_fw</td> | ||
+ | <td>pBAD_fw_FS_1</td> | ||
+ | |||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>2_fw</td> | ||
+ | <td>RT_fw_FS2_BpiI</td> | ||
+ | |||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>2_rev</td> | ||
+ | <td>RT_rev_RBS_FS_C_BpiI</td> | ||
+ | |||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>3_fw</td> | ||
+ | <td>FLPe_fw_FS_C_BpiI</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>3_rev</td> | ||
+ | <td>FLPe_rev_FS_3_BpiI</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>4_fw</td> | ||
+ | <td>RepA101ts_fw_FS_23_BsaI</td> | ||
+ | |||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>4_rev</td> | ||
+ | <td>RepA101ts_rev_FS_3_BsaI</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>5_fw</td> | ||
+ | <td>AmpR_Intron_Fw_ohne_FRT_FS_2_BsaI</td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td>5_rev</td> | ||
+ | <td>AmpR_Intron_rev_ohne_FRT_FS_3_BsaI</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>6_fw</td> | ||
+ | <td>KanR_CripsR_fw_FS_B_BsaI</td> | ||
+ | |||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>6_rev</td> | ||
+ | <td>KanR_CrispR_rev_Fs_E_BsaI</td> | ||
+ | </tr> | ||
+ | </tbody> | ||
+ | </table> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | |||
</div> | </div> | ||
</body> | </body> | ||
</html> | </html> |
Revision as of 11:52, 24 July 2017
Monday, July 3rd.
- Team discussion and overview:
- Christina, Felicia, Josef, Lisa, Magdalena, Mathias, Melanie, Michael, Mina, Rebecca, Valentin, Julian
- Planning of the procedures including primer design
- Preparing the growth media and autoclaving
- LB medium preparation (4L): Mina, Michael
- Autoclaving: Mina, Rebecca
Tuesday, July 4th.
- Planning and fundraising:
- Christina, Felicia, Josef, Lisa, Martin, Mathias, Melanie, Michael, Mina, Rebecca, Valentin, Julian
- Preparation of growth media:
- 20 plates LB medium + chloramphenicol: Mina, Lisa, Mathias
- 2 flasks LB agar: Mina, Lisa, Mathias
- Making cells from straind DH10B chemically competent as a control for the InterLab Study
Wednesday, July 5th.
- Planning and fundraising:
- Christina, Felicia, Josef, Lisa, Magdalena, Martin, Mathias, Melanie, Michael, Mina, Rebecca, Julian
- Aliquoting 1mL LB into Eppendorf tubes
- Lisa, Josef
- Transferring Backbones onto agar plates:
- Julian
- Interlab challenge - transformation: According to protocol:
- 8 transformations - from Kit Plate 6 InterLab
- 8 plasmids plated onto agar medium: Positive control (50µL, 200µL), Negative Control (50µL, 200µL), Transformant (20µL, 100µL, 200µL), Test device 1-6 (50µL, 200µL)
- stored at 35°C
- Lisa, Mathias, Michael, Mina, Rebecca
Thursday, July 6th.
- Team discussion, planning and fundraising
- Counting colonies of Transformants for the Interlab Challenge:
- Colonies 200µL: 77, 20µL: 26, 100µL: 43
- Miniprep of 8 plasmids for Golden Gate Standard - according to protocol
- Magdalena (1), Melanie (2), Valentin (3), Rebeccca (4), Christina (5), Martin (6), Mina (7), Lisa (8)
- Dilution of plasmids for Golden Gate: Lisa
Dilution sheet for Golden Gate Assembly
Sample | Volume of AD - RO Water [µL] | Volume of plasmid/fragment [µL] |
---|---|---|
BB1-C-23-Spy-Cas9(NLS)-49 | 71,6 | 28,4 |
BB1-T-34-sce-cyc-50 | 83,0 | 17,0 |
BB1-P-12-syr-pNS-J23101-25 | 85,1 | 14,9 |
BB1-P-12-sce-tdh3-45 | 82,7 | 17,3 |
BB1-T-34-eco-B1001-29 | 80,4 | 19,6 |
BB1-P-12-syn-pm-J23105-23 | 83,9 | 16,1 |
BB1-C-23-syn-GFP-30 | 82,9 | 17,1 |
BB1-P-12-sce-tef1-46 | 78,0 | 22,0 |
Friday, July 7th.
- Team discussion, Planning and Fundraising
- Interlab Challenge: Fluorescein fluorescence standard curve
- Christina
Monday, July 10th.
- InterLab Study:
- Christina, Felicia
- Dilution of several primers 1:10 (AD-RO Water µL45 , Primer µL5)
- PCR Gel Preparation
- Magdalena
- Mathias
Tuesday, July 11th.
- Planning & Fundraising
- Golden Gate Assembly:
- Dilution of several primer
- Flpe (BB1), GFP (BB2) → Transformation (according to protocol) → Plating onto Agar (After Transformation): Selection with Ampicillin (bb1), Selection with Kanamycin(bb2), stored at 37°C over night
Abbreviation | Primer |
---|---|
1_fw | pBAD_fw_FS_1 |
2_fw | RT_fw_FS2_BpiI |
2_rev | RT_rev_RBS_FS_C_BpiI |
3_fw | FLPe_fw_FS_C_BpiI |
3_rev | FLPe_rev_FS_3_BpiI |
4_fw | RepA101ts_fw_FS_23_BsaI |
4_rev | RepA101ts_rev_FS_3_BsaI |
5_fw | AmpR_Intron_Fw_ohne_FRT_FS_2_BsaI |
5_rev | AmpR_Intron_rev_ohne_FRT_FS_3_BsaI |
6_fw | KanR_CripsR_fw_FS_B_BsaI |
6_rev | KanR_CrispR_rev_Fs_E_BsaI |