Team:UT-Dallas/Notebook/8-19
From 2014.igem.org
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- | 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. </p> | + | 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. They failed the test digest so we inoculate the rest of the colonies on the plates.</p> |
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We are sending the gRNA from the third batch and some other reporter vectors for sequencing.</p> | We are sending the gRNA from the third batch and some other reporter vectors for sequencing.</p> | ||
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<LI> Purified RBS (digested overnight yesterday). | <LI> Purified RBS (digested overnight yesterday). | ||
<LI> Transformed of overnight ligation yesterday (third batch, reporter vectors with promoters under Chlora). | <LI> Transformed of overnight ligation yesterday (third batch, reporter vectors with promoters under Chlora). | ||
+ | <LI> Inoculate more colonies from ctxA, ctxB plates. | ||
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Revision as of 19:17, 19 August 2014
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. They failed the test digest so we inoculate the rest of the colonies on the plates. 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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Today's tasks: | |
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Updating the wiki notebook from the slowest computer in the building because currently we can't log into any other computer. Rishika is gel-ing the ctx-s. |