"
Team:University of Ottawa/23 July 2008
From 2008.igem.org
Revision as of 20:41, 23 July 2008 by Djedrysiak (Talk | contribs)
Contents |
Today in the lab
Dan
- PCR amplification of T123
- I wanted to do PCR amplification of 0A and 0B, however PCR blocks were full, I will do this tomorrow
- 6 tubes of PCR reaction were prepared for T123, hopefuly this will give me the amount of DNA that I need for a successful ligation.
- Transformation of p2S and p2D
- p2S and p2D were transformed in E. coli
