Haynes Lab:Notebook/RNA-seq of PcTF Transfected U2OS & SK-N-SH cell lines/2015/05/27: Difference between revisions

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Treat samples in duplicate, for 12 samples in total.
Treat samples in duplicate, for 12 samples in total.
==Notes==
Culture density: 240,000 cells/mL * 5 mL culture = 1.2E6 cells total
To make 1E7 cells/mL concentration, spin down and resuspend in 120 µL Resuspension Buffer R.


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Revision as of 15:11, 27 May 2015

Neon transfection of K562 cell line <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
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Overview

Trying transfection of K562 again, this time using the Neon transfection system.

Protocol

  1. Set up a 12 well plate with 1 mL of antibiotic-free medium in each well. Place in the incubator.
  2. Spin down 5 mL of K562 culture and wash with PBS. Check density using hemocytometer. Spin down again, resuspend in approximate volume of Resuspension Buffer R to get 1E7 cells/mL using Resuspension Buffer R. Check density again using hemocytometer.
  3. Follow the instructions on page 2 of the Neon Transfection System reference card to proceed.

Samples:

  1. pMax GFP, 1000 v, 50 ms, 1 pulse
  2. pMax GFP, 1350 v, 10 ms, 4 pulses
  3. pMax GFP, 1450 v, 10 ms, 3 pulses
  4. KAH126-MV2, 1000 v, 50 ms, 1 pulse
  5. KAH126-MV2, 1350 v, 10 ms, 4 pulses
  6. KAH126-MV2, 1450 v, 10 ms, 3 pulses

Treat samples in duplicate, for 12 samples in total.

Notes

Culture density: 240,000 cells/mL * 5 mL culture = 1.2E6 cells total

To make 1E7 cells/mL concentration, spin down and resuspend in 120 µL Resuspension Buffer R.



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