EPF-Lausanne/12 October 2009
From 2009.igem.org
(Difference between revisions)
(→Wet Lab) |
(→Wet Lab) |
||
Line 36: | Line 36: | ||
Took image of agarose gel: | Took image of agarose gel: | ||
[[Image:121009gel_DTjrg1046.JPG|200px|thumb|left]] | [[Image:121009gel_DTjrg1046.JPG|200px|thumb|left]] | ||
+ | <br><br> | ||
RO1.1+BB1 #3 and 6 are double transformants: | RO1.1+BB1 #3 and 6 are double transformants: |
Revision as of 08:50, 18 October 2009
Contents |
Wet Lab
Digestion assay (with Pst1 and SpeI) in order to check the double transformant -KO strand JRG1046.
We checked 3 clones of each double transformant: RO1.1+BB1 and RO2.4+BB1.
N.B: RO1.1+BB1 clone #1 culture wasn't pink at all
Took image of agarose gel:
RO1.1+BB1 #3 and 6 are double transformants:
( cut RO1 --> band of ~900bp, plasmid-900bp
RO2 --> band of 1.8 kb, plasmid - 1.8 kb
BB --> band of ~ 200bp, 400bp, plasmid - 600bp )
Started protocol to clone the "simple" LovTap into an iGEM plasmid: did the PCR on LovTap with primers that contained the iGEM prefix and suffix
People in the lab
Tú, Heidi