EPF-Lausanne/12 October 2009
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==Wet Lab== | ==Wet Lab== | ||
Digestion assay (with Pst1 and SpeI) in order to check the double transformant -KO strand JRG1046. | Digestion assay (with Pst1 and SpeI) in order to check the double transformant -KO strand JRG1046. | ||
- | We | + | |
+ | 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 | N.B: RO1.1+BB1 clone #1 culture wasn't pink at all | ||
- | |||
- | RO1.1+BB1 #3 and 6 are double | + | |
+ | Took image of agarose gel: | ||
+ | [[Image:121009gel_DTjrg1046.JPG|200px|thumb|center]] | ||
+ | <br><br> | ||
+ | |||
+ | RO1.1+BB1 #3 and 6 are double transformants: | ||
+ | |||
( cut RO1 --> band of ~900bp, plasmid-900bp | ( cut RO1 --> band of ~900bp, plasmid-900bp | ||
+ | |||
RO2 --> band of 1.8 kb, plasmid - 1.8 kb | RO2 --> band of 1.8 kb, plasmid - 1.8 kb | ||
+ | |||
BB --> band of ~ 200bp, 400bp, plasmid - 600bp ) | 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== | ==People in the lab== |
Latest 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