Team:Paris Liliane Bettencourt/Notebook/2011/08/27/
From 2011.igem.org
Danyel
pT7+RBS+GFP+Ter
Camille
Transformation seemed to work. To verify the construct was really in my strains I decided to do a PCR colony for five clones. I used for that the primers VF2 and VR. I also digested minipreps from Danyel of the strains containing the tRNA one strain with a terminator behind the second one without. In order to clon the pHyperspank before the tRNA. I did a gel, extracted the bands. I obtained good [DNA], 12.8ng/µL fr the tRNA + terminator strain and 17.9ng/µL for the other one.
I launched the ligation overnight.
The PCR colony resulted in the selection of two over the five clones that looked good. I launched them for an overnight liquid culture.