Team:Calgary/1 July 2009
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I replied back to company emails and tried my best to answer their questions about our project. I researched a few old companies who had declined our proposals and searched new contacts in different departs. I will call them tomorrow. | I replied back to company emails and tried my best to answer their questions about our project. I researched a few old companies who had declined our proposals and searched new contacts in different departs. I will call them tomorrow. | ||
+ | |||
+ | '''In the lab''' | ||
+ | Shadowed Vicky with Colony PCR of J13002 + JuxOD47A BBk + B0015 on pSB1AK3 | ||
+ | Purpose: The bacterial culture growth is prolific. This will verify if the proper gene constructs are included within. | ||
+ | |||
+ | Materials an methods: | ||
+ | |||
+ | * Primers: BBk forward and reverse construction primers | ||
+ | * Master mix: Use pTaq DNA polymerase. The contents will suffice for 15 tubes, and were prepared in the same fashion as on June 26. | ||
+ | * PCR conditions: These are also the same as they were on June 26 | ||
+ | |||
+ | Tubes 1/6 were colony 1 | ||
+ | |||
+ | tubes 2/7 were col 2 | ||
+ | |||
+ | tubes 3/8 were col 3 | ||
+ | |||
+ | tubes 4/9 were col 4 | ||
+ | |||
+ | tubes 5/10 were col 5 | ||
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Revision as of 08:16, 21 August 2009
UNIVERSITY OF CALGARY