User:Karmella Haynes/Notebook/PcTF Genomics/2013/06/11: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Pc-TF Genomics</span>
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Pc-TF Genomics</span>
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==06/11/13==
==06/11/13==
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* Gal4-EED/luc HEK +dox cytology: fix and stain cells with primary ab
* Gal4-EED/luc HEK +dox cytology: fix and permeabilize cells
 


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* Use David Dreher's protocol, except dilute dry paraformaldehyde to make fresh fixing buffer.
* Use David Dreher's protocol, except dilute dry paraformaldehyde to make fresh fixing buffer.
* Process all 24 wells


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Latest revision as of 22:45, 26 September 2017

Pc-TF Genomics Main project page
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06/11/13

  • Gal4-EED/luc HEK +dox cytology: fix and permeabilize cells



Gal4-EED/luc HEK +dox cytology
> Use 24-well plate from 6/10/13

  • Use David Dreher's protocol, except dilute dry paraformaldehyde to make fresh fixing buffer.
  • Process all 24 wells