User:Karmella Haynes/Notebook/PcTF Genomics/2013/06/03

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(06/03/13)
Current revision (17:48, 11 June 2013) (view source)
(06/03/13)
 
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* Ran samples 6 (blank), 1, 2, and 3 and recorded SS, FS, and mCherry
* 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.
* Very modest mCh over background (blank). Tong noted that the mCherry laser was not optimal for this fluorophore.
 +
** ~1% RFP+ over background (with gating)

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06/03/13

  • Flow cytometry of PcTF+ U2OS cells

Flow cytometry at Biodesign

Samples:

  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)

Harvesting:

  • 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).



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