Notebook
August 16, 2010
- We started the cloning procedure.
- We digested some of the parts and then gel purified them. All but two worked.
- We incubated some of the glycerol stock of the two that did not work.
Image 1: There is a 2-log DNA ladder, then there is not a correct band for Pu, then there is a band for PyeaR
Image 2: There is a 2-log DNA ladder, then Pr+XylR correct, then Terminator incorrect, then Red correct, then GFP correct, then Orange correct, then mRFP1 correct, and then a 1 kb DNA ladder