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Team:TUDelft/24 August 2009
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| + | Prepare IPTG 1M for further induction. I tried to do an experiment with 1A which is GFP under control of PLacI however the culture glows even though there is no IPTG induction. | ||
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| + | We got the oligo for the two locks and keys I designed. | ||
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Revision as of 16:47, 29 August 2009
Lab Notebook
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24 August 2009
Transformaltion of friday 21-08-2009 looked good. On each plate there were 80-90 kolonies
Daniel
Digestion of assemblies in order to do the second round of assembly. Gel 1% (left) for Calin´s PCR and 2% (right) for my digestions and Calin´s PCR
Right Gel (2%)
| Well | Assembly | Expected Plasmid Size | Status |
| 1 | [http://www.eurogentec.com/EGT/Images/RESALES/Electrophoresis/Regular%20DNA%20Ladder/7-SmartLadder.jpg DNA Ladder] | ✔ | |
| 2 | 4A | 824 | ? |
| 3 | 5A | 1040 | ✔ |
| 4 | 2A | 214 | ? |
| 5 | 3A | 183 | ? |
| 6 | 1A | 1076 | ? |
| 7 | PCR 1 | ||
| 8 | PCR 2 | ||
| 9 | PCR 3 | ||
| 10 | PCR 4 | ||
| 11 | PCR 5 | ||
| 12 | PCR 6 |
Prepare IPTG 1M for further induction. I tried to do an experiment with 1A which is GFP under control of PLacI however the culture glows even though there is no IPTG induction.
We got the oligo for the two locks and keys I designed.
