Team:Groningen/Labwork/27 September 2013
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<h2>Claudio</h2> | <h2>Claudio</h2> | ||
- | Starch assay was performed on the 6 colonies which were inoculated yesterday. | + | Starch assay was performed on the 6 colonies which were inoculated yesterday (<b>Sander</b>). |
<br><img src="https://static.igem.org/mediawiki/2013/1/1d/Starch_assay_BB18_BB22.jpg" width="50%"> | <br><img src="https://static.igem.org/mediawiki/2013/1/1d/Starch_assay_BB18_BB22.jpg" width="50%"> | ||
<br> | <br> | ||
- | <br>Colony PCR was also performed on the same 6 colonies. The pair of primers used was F-hy_spank-NheI and HM14 (annealing temperature 70°C). | + | <br>Colony PCR was also performed on the same 6 colonies. The pair of primers used was F-hy_spank-NheI and HM14 (annealing temperature 70°C) (<b>Sander</b>). |
- | <br>The samples were checked on agarose gel 0.8%. | + | <br>The samples were checked on agarose gel 0.8% (<b>Inne</b>). |
<br><img src="https://static.igem.org/mediawiki/2013/3/34/ColonyPCR_Bs_BB18_BB22_26-09-2013.jpg" width="50%"> | <br><img src="https://static.igem.org/mediawiki/2013/3/34/ColonyPCR_Bs_BB18_BB22_26-09-2013.jpg" width="50%"> | ||
<br>The samples showed to be all positive candidates (expected product size ~2400bps). | <br>The samples showed to be all positive candidates (expected product size ~2400bps). | ||
<br> | <br> | ||
- | <br>Colony 1 from each transformation didn't show any amylase activity and show positive results from the Colony PCR screening, therefore 100µl of O/N liquid culture were inoculated in | + | <br>Colony 1 from each transformation didn't show any amylase activity and show positive results from the Colony PCR screening, therefore 100 µl of O/N liquid culture were inoculated in 50 mL LB. |
- | <br>The cultures were induced when the OD<sub>600</sub> was 0.5 with | + | <br>The cultures were induced when the OD<sub>600</sub> was 0.5 with 1 mM IPTG. |
<br>Samples were taken every hour after induction and without any induction. | <br>Samples were taken every hour after induction and without any induction. | ||
+ | <p> | ||
<h2>Mirjam</h2> | <h2>Mirjam</h2> | ||
A colony PCR is done for EstA-S3 and EstA-S9. This showed correct clones for both of the ligation reactions. So an inoculation is done for these samples. | A colony PCR is done for EstA-S3 and EstA-S9. This showed correct clones for both of the ligation reactions. So an inoculation is done for these samples. | ||
<br><img src="https://static.igem.org/mediawiki/2013/f/f6/EstA_%2B_S3-S9.jpg" width="50%"> | <br><img src="https://static.igem.org/mediawiki/2013/f/f6/EstA_%2B_S3-S9.jpg" width="50%"> | ||
+ | <br> | ||
+ | <br>Did a restriction analysis on Pdes-CheY to check if the transformation is performed correctly. The same restriction digestion is done for biobrick BBa_K823823. The restriction digest went well, so gel purification can be done. | ||
+ | <br><img src="https://static.igem.org/mediawiki/2013/b/bb/Pdes-CheY%2C_BBa_k823823%2C_restriction_digest_with_E-P.png" width="50%"> | ||
+ | <br> | ||
+ | <br>Did a new transformation of CheC into the ΔCheYΔDes knock out strain. | ||
+ | <br>Started further purification of the ΔCheY and ΔCheYΔDes strains on plate. | ||
+ | </p> | ||
</div> | </div> |
Latest revision as of 19:50, 27 September 2013
Claudio
Starch assay was performed on the 6 colonies which were inoculated yesterday (Sander).Colony PCR was also performed on the same 6 colonies. The pair of primers used was F-hy_spank-NheI and HM14 (annealing temperature 70°C) (Sander).
The samples were checked on agarose gel 0.8% (Inne).
The samples showed to be all positive candidates (expected product size ~2400bps).
Colony 1 from each transformation didn't show any amylase activity and show positive results from the Colony PCR screening, therefore 100 µl of O/N liquid culture were inoculated in 50 mL LB.
The cultures were induced when the OD600 was 0.5 with 1 mM IPTG.
Samples were taken every hour after induction and without any induction.
Mirjam
A colony PCR is done for EstA-S3 and EstA-S9. This showed correct clones for both of the ligation reactions. So an inoculation is done for these samples.Did a restriction analysis on Pdes-CheY to check if the transformation is performed correctly. The same restriction digestion is done for biobrick BBa_K823823. The restriction digest went well, so gel purification can be done.
Did a new transformation of CheC into the ΔCheYΔDes knock out strain.
Started further purification of the ΔCheY and ΔCheYΔDes strains on plate.