Electroporation of nec: Difference between revisions
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== | == Material == | ||
Culture media: | |||
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!style="width: 300px" | Name | !style="width: 300px" | Name | ||
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|For lower passages only | |For lower passages only | ||
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== Procedure == | |||
# Incubate NSC 60-90min with 1mM DPBS/EDTA | |||
# Prepare 1.5ml tubes with DNA mix (max. 3µg/µl, 0.75-1µg/µl per plasmid). Max. 3µl DNA mixture | |||
# Prepare 12well plate with gelatine | |||
# Prepare Culture Media | |||
# Centrifuge cells for 3min at 700g | |||
# Resuspend one flask (75cm2) with cells after centrifugation in 160µl Steinberg solution | |||
# Add 12µl each of the cell suspension to every DNA mix | |||
# Electroporation conditions are: 500V, 50ms, 5 pulses | |||
# Add cells to the plate and check after 1 day | |||
Revision as of 09:21, 25 March 2015
Material
Culture media:
| Name | Quantity | Remarks |
|---|---|---|
| Glutamax | DMEM:F12 | |
| Glutamin | 10µl/ml | |
| Pen/Strep | 10µl/ml | |
| B27 (50x) | 20µl/ml | |
| FGF2 (20µg/ml) | 20ng/ml | |
| Shh (Curis) | 100ng/ml | For lower passages only |
Procedure
- Incubate NSC 60-90min with 1mM DPBS/EDTA
- Prepare 1.5ml tubes with DNA mix (max. 3µg/µl, 0.75-1µg/µl per plasmid). Max. 3µl DNA mixture
- Prepare 12well plate with gelatine
- Prepare Culture Media
- Centrifuge cells for 3min at 700g
- Resuspend one flask (75cm2) with cells after centrifugation in 160µl Steinberg solution
- Add 12µl each of the cell suspension to every DNA mix
- Electroporation conditions are: 500V, 50ms, 5 pulses
- Add cells to the plate and check after 1 day