Isolation of Mouse Embryonic Fibroblasts (MEFs): Difference between revisions
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copied in protocol from sergey's paper |
updated with more details |
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Line 1: | Line 1: | ||
From Zolov et al (under review) | From Zolov et al (under review) | ||
==Materials== | |||
* Collagenase, type II (LS004204, Worthington, US) | |||
* Clean surgical blades | |||
* DMEM/PSG/10% FBS | |||
==Generation of Mouse Primary Fibroblast Cells== | ==Generation of Mouse Primary Fibroblast Cells== | ||
# MEFs were prepared from tails and legs of P0 pups. | |||
# Disect out all four limbs plus the tail. Place one small piece into PCR tube/plate for genotyping | |||
# Using a clean surgical blade, chop into tiny pieces. | |||
# Place into 5 mL of collagenase in DMEM/PSG/10% Serum (500U/mL) in a 15 mL falcon tube | |||
# Incubate in incubator for 12 hours at 37°C. | |||
# After incubation, cells were harvested at 200 g for 5 min | |||
# Wash cells once with warm media, then resuspend in DMEM. | |||
# Plate into 2-3 100 mm dishes and change media afer 1d | |||
# Split when confluent |
Latest revision as of 15:50, 5 September 2012
From Zolov et al (under review)
Materials
- Collagenase, type II (LS004204, Worthington, US)
- Clean surgical blades
- DMEM/PSG/10% FBS
Generation of Mouse Primary Fibroblast Cells
- MEFs were prepared from tails and legs of P0 pups.
- Disect out all four limbs plus the tail. Place one small piece into PCR tube/plate for genotyping
- Using a clean surgical blade, chop into tiny pieces.
- Place into 5 mL of collagenase in DMEM/PSG/10% Serum (500U/mL) in a 15 mL falcon tube
- Incubate in incubator for 12 hours at 37°C.
- After incubation, cells were harvested at 200 g for 5 min
- Wash cells once with warm media, then resuspend in DMEM.
- Plate into 2-3 100 mm dishes and change media afer 1d
- Split when confluent