"
Copenhagen/7 July 2011
From 2011.igem.org
(Difference between revisions)
| Line 5: | Line 5: | ||
| - | === | + | ===Lab Work=== |
* PCR purification of A1 | * PCR purification of A1 | ||
| Line 14: | Line 14: | ||
| - | ===Other | + | ===Other Work=== |
*We have answered many e-mails from danish companies associated with the biotech industry. Some supported us morally and a few economically. We a looking forward to recieve positive answers from the rest of the companies. | *We have answered many e-mails from danish companies associated with the biotech industry. Some supported us morally and a few economically. We a looking forward to recieve positive answers from the rest of the companies. | ||
Latest revision as of 12:34, 7 July 2011
Thursday
The transformation of Cyp79B1 went well, we have a lot of colonies. The sequentation of A1 showed that it was not mutated.
Lab Work
- PCR purification of A1
- Mutation and transformation of A1 and A2 with an other amount of template (from 10/50 ng to 25 ng)
- Overnight culture of B1 (2 of each template concentration).
Other Work
- We have answered many e-mails from danish companies associated with the biotech industry. Some supported us morally and a few economically. We a looking forward to recieve positive answers from the rest of the companies.
Back to notebook
