Electroporation of A1 cells: Difference between revisions

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# Wash pellet with Steinberg's solution and resuspend in 300 µl of Steinberg's, keep on ice
# Wash pellet with Steinberg's solution and resuspend in 300 µl of Steinberg's, keep on ice
# Before electroporation, make sure to electroporate a cuvette with no cells to discharge device
# Before electroporation, make sure to electroporate a cuvette with no cells to discharge device
# Electroporate cells in following conditions and put back on ice:
# Electroporate cells in following conditions and put back on ice: Myoblasts: 100V, 35 msec, 5 pulses, Myotubes: 75 V, 35 msec, 5pulses
Myoblasts: 100V, 35 msec, 5 pulses
Myotubes 75 V, 35 msec, 5pulses
# Plate cells as normal
# Plate cells as normal



Revision as of 07:24, 5 September 2014

Materials:

  • Ice
  • 4 mM cuvettes, N+1 cuvettes
  • Steinberg's, at 4 C.
  • Square pulse electroporator (we use the BTX 830 Squarporator)
    1. Put cuvettes on ice, and cool down Steinberg's on ice
    2. Trypsinize cells as normal, stop reaction with high serum media and spin down at 1000 rpm, 3 minutes
    3. Wash pellet with Steinberg's solution and resuspend in 300 µl of Steinberg's, keep on ice
    4. Before electroporation, make sure to electroporate a cuvette with no cells to discharge device
    5. Electroporate cells in following conditions and put back on ice: Myoblasts: 100V, 35 msec, 5 pulses, Myotubes: 75 V, 35 msec, 5pulses
    6. Plate cells as normal

    Steinberg's

    1x FW (MW) 5x/500 ml 58 mM NaCl 58.44 8.47 g

    0.67 mM     KCl	74.56	1.68 ml (1M)
    0.44 mM   Ca(NO3)	236.20	1.1 ml (1M)
    1.3   mM     MgSO4	246.47	3.25 ml (1M)
    4.6   mM     Tris pH  7.8-8.0		5.75 ml (2M)