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EPF-Lausanne/14 October 2009
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[[Image:141009_dh5_ro2dt_2h30.jpg|center|thumb|upright=4|RO2 double-transformants in DH5-alpha]] | [[Image:141009_dh5_ro2dt_2h30.jpg|center|thumb|upright=4|RO2 double-transformants in DH5-alpha]] | ||
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| + | '''RO1.1 + BB1 JRG1046 cells''' | ||
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| + | Did an experiment on the new double-transformants for RO1 in the TrpR-mutated strains: 0.5 mL of overnight culture in 3.5 mL of fresh LB. Since we had 4 different clones, for 3 of them we did only the +light+IPTG and -light+IPTG conditions, and for the 4th one we added the -light-IPTG+/-Trp conditions. The cells were exposed to conditions during about 2h before we took the measurements of OD and fluorescence with the plate reader. | ||
==People in the lab== | ==People in the lab== | ||
Revision as of 10:50, 17 October 2009
Contents |
Wet Lab
Transformation of LOVTAP in iGEM plasmid worked --> Check if the insert is correct with Colony PCR & agarose gel
Also: our negative control worked (no clones grew)
Dh5-alpha RO2.4+BB1 n°3
We redid the initial experiment with these cells: incubated them for about 2h30 in 4 different conditions:
- +light+IPTG-Trp
- -light+IPTG-Trp
- -light-IPTG+Trp
- -light-IPTG-Trp
The results are the following:
RO1.1 + BB1 JRG1046 cells
Did an experiment on the new double-transformants for RO1 in the TrpR-mutated strains: 0.5 mL of overnight culture in 3.5 mL of fresh LB. Since we had 4 different clones, for 3 of them we did only the +light+IPTG and -light+IPTG conditions, and for the 4th one we added the -light-IPTG+/-Trp conditions. The cells were exposed to conditions during about 2h before we took the measurements of OD and fluorescence with the plate reader.
People in the lab
Gabriela, Tú
