Team:Trieste/notebook10

From 2012.igem.org

Revision as of 17:47, 24 September 2012 by Samarisara (Talk | contribs)

Week 10

More

Suicide System

We transformed also the double terminator (BBa_B0015) as Bglbrick. We amplified by PCR the BBa_B0015 miniprep with the appropriate PCR protocol. We loaded the gel with the amplified and the eluted was ligated in the pGEM vector.

The plasmid was amplified with the primers SP6 and T7 and then cut BglII/XhoI.

For the final construct -holin LL 37- : the LL 37 (BBa_K875009) was cloned downstream the T5CumateOperator (BBa_K875001), heat inactivated and dephosphorylated at the extremities.

Antibody

We developed an E.L.I.S.A. test to check out if LPP-OmpA-scFv is displayed on bacterial surface. We tried to immobilize the bacteria expressing our antibody on E.L.I.S.A. plates. This experiment had no success probably because it was not optimized enough.

Chassis

Lorem ipsum dolor sit amet, consectetur adipisicing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.
Team iGEM 2012

Contact us

For other information, write to:

igem2012@gmail.com
Università degli studi di Trieste ICGEB Illy Fondazione Cassa di Risparmio
iGEM 2012 iGEM 2012 iGEM 2012 iGEM 2012 iGEM 2012 iGEM 2012
HTML Hit Counter