Team:UT-Dallas/Notebook/8-04

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Monday, August 4th, 2014

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Today we did a gel purification of our overnight digested promoter, inoculated any color colonies from chromoproteins,transformed ligation's for reporter vectors, and prepared gRNA vectors for sequencing

Tentative plan for tomorrow

Today's tasks:

Ligation. (over-night)

Digest more promoters.

Gel & gel purify reporter vectors.
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Colonies!!!!

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