Team:Groningen/4 July 2013

From 2013.igem.org

(Difference between revisions)
Line 36: Line 36:
</table>
</table>
1. = duplo of sample 1
1. = duplo of sample 1
 +
 +
Ran the same gel again for 22 min on 100 volt to get a better picture

Revision as of 19:36, 4 July 2013

Sander and Inne


For the silk it is decided to try a PCR with an annealing temperature of 85 and 90 degrees Celsius. we followed the usual protocol aside from the standard diluted template DNA but also tried undiluted template DNA 1, (ul in 50 ul mix for both of then) .
1 2 3 4 5 6
98 98 85/90 72 72 4
20:00 0:30 0:25 0:27 10:00 forever

Ran a gel with the 8 PCR products and the purified promoter from yesterday (as a check).

Well 1 2 3 4 5 6 7 8 9 10
promoter Marker 1 1. 2 2. 3 3. 4 4.

1. = duplo of sample 1

Ran the same gel again for 22 min on 100 volt to get a better picture