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EPF-Lausanne/21 July 2009
From 2009.igem.org
(New page: ===Wet Lab=== The transformation of the Term plasmids worked, so we did glycerol stocks of the 4 new Term and the death cassette. Then miniprep of the 5 transformation products. Digestio...) |
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The restriction site used were: | The restriction site used were: | ||
| - | <br>EcoRI | + | <br>EcoRI {{pad|4em}} GAATTC |
<br>XbaI TCTAGA | <br>XbaI TCTAGA | ||
<br>SpeI ACTAGT | <br>SpeI ACTAGT | ||
Revision as of 15:52, 27 July 2009
Wet Lab
The transformation of the Term plasmids worked, so we did glycerol stocks of the 4 new Term and the death cassette.
Then miniprep of the 5 transformation products.
Digestion following the iGEM protocol : we cut with X and P Term, E and P the backbone and we take a LovTAP that was digested Friday with E and S.
Running of a gel to check the digestion products. Actually it seems the digestion didn't work. We did a second gel, by loading more product, and we clearly got the same result.
As the ligation this way seems not to work (either the enzymes for the digestion aren't working, either there is another problem in the ligation), we decided to try another way to do it : by doing a 2 step PCR. We designed and ordered the primers, now we just have to wait for them to go on in our cloning of LovTAP. Have a look at the cloning strategy to see how we designed the primers.
The idea of 2 step PCR : Media:2step pcr.pdf
Cloning Strategy
One useful website to know the restriction sites of enzymes:
http://www.genscript.com/cgi-bin/products/enzyme.cgi?op=all_ez
The restriction site used were:
EcoRI Template:Pad GAATTC
XbaI TCTAGA
SpeI ACTAGT
PsiI TTATAA
Design the primers for the 2 step-PCR: the first step introduces the LacI promoter and the RBS upstream the LovTAP gene with the Forward primer, whereas the Reverse introduces the Term downstream. In the second step we only introduce the E-X restriction sites upstream and the SP downstream.
