Team:EPF-Lausanne/Last News
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*The second biobrick was coloned as well, but we wait for the results to confirm that the plasmid contain the right insert | *The second biobrick was coloned as well, but we wait for the results to confirm that the plasmid contain the right insert | ||
*Modeling part: Preliminar simulations were lauched, and their analysis were done, simulations will be lauched in few days. | *Modeling part: Preliminar simulations were lauched, and their analysis were done, simulations will be lauched in few days. | ||
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==''(12.07.09)''== | ==''(12.07.09)''== |
Revision as of 08:06, 1 August 2009
Keep track with what we did so far
(01.08.09)
- This fourth week of wetlab we have done the following things
- Our gene of interest (photoreceptor LOVTAP) was cloned in front of a terminator (iGEM part BBa_B0015). We created our first biobrick.
- The second biobrick was coloned as well, but we wait for the results to confirm that the plasmid contain the right insert
- Modeling part: Preliminar simulations were lauched, and their analysis were done, simulations will be lauched in few days.
(12.07.09)
- This first week of wetlab we have done the following things
- Transformed the plasmids with the LovTAP gene, generously sent by Dr. Sosnick's lab from Chicago universtiy, into competent E.Coli
- Designed the cloning strategy for cloning the LovTAP gene from its original vector to a iGEM vector+add an inducible promoter (LacI) (+RBS +term.)
- Ordered and received the primers needed for the PCR of LovTAP
- Designed the cloning strategy for inclusion of the LovTAP BioBrick with different reporting cassettes
- Transformed all the BioBricks that will be needed for the cloning strategies (c.f. notebook for more information about these parts) into competent E.Coli
- Fused the two BioBricks "LacI" and "RBS"
- Digested the LovTAP PCR products and RBS part