Team:EPF Lausanne/Calendar/29 July 2013

From 2013.igem.org

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'''Cell Surface Display'''
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''PCR optimisation:'' the previour PCR we did to amplify ''pINP_construct'' was not optimal. We thus did another gradient PCR of the same plasmid with 5% DMSO at 74, 76 and 78°C.
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A 0.8% Electrophoresis gel was performed to verify the reation's products.
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Revision as of 14:55, 1 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Cell Surface Display

PCR optimisation: the previour PCR we did to amplify pINP_construct was not optimal. We thus did another gradient PCR of the same plasmid with 5% DMSO at 74, 76 and 78°C. A 0.8% Electrophoresis gel was performed to verify the reation's products.