Difference between revisions of "User:Karmella Haynes/Notebook/PcTF Genomics/2013/06/03"

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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>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
|style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
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Latest revision as of 22:45, 26 September 2017

Owwnotebook icon.pngPc-TF Genomics Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png


  • Flow cytometry of PcTF+ U2OS cells

Flow cytometry at Biodesign


  1. 2.0 μg plasmid/ 1x106 cells
  2. 1.0 μg
  3. 0.5 μg
  4. 0.2 μg
  5. 0.1 μg
  6. blank (no transfection)


  • Detached cells w/ 0.5 mL trypsin medium
  • Pelleted in ab-free medium
  • Washed once with 1xPBS buffer. Resuspended in 0.5 mL 1xPBS

Flow cytometry:

  • Took cells over the BDI on ice. Strained cells once through cell strainer caps (purchased 10 from Tong Xu); forced cells through cap with pipette (did not centrifuge)
  • Ran samples 6 (blank), 1, 2, and 3 and recorded SS, FS, and mCherry
  • Very modest mCh over background (blank). Tong noted that the mCherry laser was not optimal for this fluorophore.
    • ~1% RFP+ over background (with gating)

Flow cytometry - Wang Lab's Accuri C6

  • Diluted samples 3x to get reads per sec. down to 240
  • Signal over background looked pretty good for mCherry
  • Drawback is that voltage/ sensitivity cannot be adjusted, so blank signal is in the 103 range.
  • Do further tests to see if Accuri GFP settings can detect CFP (AmCyan).