Team:UT-Dallas/Notebook/8-19
From 2014.igem.org
Tuesday, August 19, 2014
Today is a short day. Yesterday, we picked 2 colonies from each failed clone plates and inoculate them; today, we minipreped and test digested them. We are sending the gRNA from the third batch and some other reporter vectors for sequencing. Yesterday, we digested more RBS-Carb; today, we ran it on gel and gel purified it. The concentration at the end was good. Our clones on the plates transformed yesterday were good: many colonies on the plates and none on the negative.
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