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− | === | + | ====Low Fidelity Dreamtaq PCR of transformed DH5α with pPS16_002==== |
+ | ''By Mathilde'' | ||
+ | |||
+ | A DreamTaq PCR was made with [[Team:Paris_Saclay/Notebook/July/19#Visualization|transformed]] cultures pPS16_002 following the usual [[Team:Paris_Saclay/Experiments#Polymerase_chain_reaction|protocol]] with Tm at 57°c and 5min for the initial denaturation. | ||
+ | |||
+ | We divided up the PCR mix in 6 PCR tubes and added in each one a different clone from the transformed culture. | ||
+ | The picked colonies were re-plated on a petri dish medium LB + Ampicillin (50µg/mL) + xGal/IPTG (1/1000). | ||
+ | |||
+ | Results : | ||
+ | PCR products expected were : | ||
+ | {| class="wikitable" | ||
+ | |- | ||
+ | !'''Plasmid''' | ||
+ | !pPS16_002 | ||
+ | |- | ||
+ | !'''Bande Size pb''' | ||
+ | |960 | ||
+ | |} | ||
+ | |||
+ | |||
+ | The electropheresis on agarose gel showed absolutely no PCR products. From this day, transformed culture from the 22/07/2016 will be used for the PCR experiments instead of those from the 19/07/2016. | ||
+ | |||
+ | |||
Revision as of 13:28, 22 July 2016