Haynes Lab:Notebook/HPK-CFP insertion into Gal4EED/Luc using CRISPR/2015/11/24: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Today's project is...</span>
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Latest revision as of 01:21, 27 September 2017

Today's project is... Main project page
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Overview

Waiting for new primers to arrive. In the meantime, attempted ligation of LCR product into pJET vector followed by transformation into DH5α-Turbo competent E. coli.

Method

Ligation

Used 3.5 µL of LCR product and 50 ng of pJET vector. Total ligation volume 10 µL.

Transformation

Two plates set up: sample containing cells transformed with ligation product, and negative control containing pJET only. Expect to see no colonies on pJET control due to kill gene.