Team:Calgary/22 July 2010
From 2010.igem.org
Notebook
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||
Thursday July 22, 2010
Himika
Today I miniprepped 10 colonies from the I0500-B0034 construction using Sigma-Aldrich kit. I also did a plasmid switch of I0500-B0034 from pSB1A3 to pSB1AC3.
Jeremy
Today I did a colony PCR of K23900+I13507, K239000+I13504, K135000+I13507, K135000+I13504 and prepared an overnight of several colonies. I also re-ligated and transformed I0500+B0034 in pSB1AC3 plasmid.
Chris
Today, I calculated the values of the enzymes we received from New England Biolabs. As well, I redid the gel of the colony PCR of the CpxP promoter with a 1.0% gel. This time, the DNA actually moved and the picture of the gel can be seen on the right. However, the bands were very non-specific. To optimize, I set up one gradient PCR with temperature of annealing step ranging from 53-58°C.
No notebook page exists for this date. Sorry!