Electroporation of A1 cells: Difference between revisions

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==Materials:==
== Material ==
<li> Ice
* Ice
<li> 4 mM cuvettes,  N+1 cuvettes
* 4 mM cuvettes,  N+1 cuvettes
<li> Steinberg's, at 4 C.
* Steinberg's, at 4 C.
<li> Square pulse electroporator (we use the BTX 830 Squarporator)
* Square pulse electroporator (we use the BTX 830 Squarporator)


''Steinberg's''
{| class="wikitable"
!style="width: 150px" | 1x
!style="width: 100px" | FW (MW)
!style="width: 100px" | 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)
|}
== Procedure ==
# Put cuvettes on ice, and cool down Steinberg's on ice
# Put cuvettes on ice, and cool down Steinberg's on ice
# Trypsinize cells as normal, stop reaction with high serum media and spin down at 1000 rpm, 3 minutes  
# Trypsinize cells as normal, stop reaction with high serum media and spin down at 1000 rpm, 3 minutes  
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# Electroporate cells in following conditions and put back on ice: Myoblasts: 100V, 35 msec, 5 pulses, Myotubes: 75 V, 35 msec, 5pulses
# Electroporate cells in following conditions and put back on ice: Myoblasts: 100V, 35 msec, 5 pulses, Myotubes: 75 V, 35 msec, 5pulses
# Plate cells as normal
# Plate cells as normal
==Steinberg's==
{| class="wikitable"
!style="width: 300px" | 1x
!style="width: 200px" | FW (MW)
!style="width: 200px" | 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)

Latest revision as of 14:25, 8 June 2015

Material

  • Ice
  • 4 mM cuvettes, N+1 cuvettes
  • Steinberg's, at 4 C.
  • Square pulse electroporator (we use the BTX 830 Squarporator)


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)


Procedure

  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