Haynes Lab:Notebook/CRISPR Editing/2015/05/27: Difference between revisions
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==05/27/2015== | ==05/27/2015== | ||
Redo qPCR with the right control primers<br> | Redo qPCR with the right control primers, TBP<br> | ||
Dilutions for 2ng gDNA per well: | Dilutions for 2ng gDNA per well: | ||
{| {{table}} | {| {{table}} |
Revision as of 17:23, 27 May 2015
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05/27/2015Redo qPCR with the right control primers, TBP
Make these mixes for each primer pair, add 36.75 to each triplicate tube, then pipette 15ul into 3 well of the plate. |