"
Copenhagen/7 July 2011
From 2011.igem.org
(Difference between revisions)
(Blanked the page) |
|||
| Line 1: | Line 1: | ||
| + | ==Thursday== | ||
| + | The transformation of Cyp79B1 went well, we have a lot of colonies. | ||
| + | The sequentation of A1 showed that it was not mutated. | ||
| + | |||
| + | |||
| + | ===Labwork=== | ||
| + | |||
| + | * PCR purification of A1 | ||
| + | |||
| + | * [[Team:Copenhagen/Protocol#Mutations|Mutation]] and [[Team:Copenhagen/Protocol#Transformations|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. | ||
Revision as of 12:26, 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.
Labwork
- 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.
