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You are here:Home » Culture Media » Media-Cell Culture » Endothelial Progenitor Outgrowth Cells, Mouse, Freezing Medium

Endothelial Progenitor Outgrowth Cells, Mouse, Freezing Medium

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Specifications

Catalog #E3010-72F
DescriptionMouse EPOC freezing medium was optimized for cryopreservation of our Mouse endothelium progenitor Outgrowth cells (mEPOC).
This product contains fetal bovine serum. Each lot is tested for sterility.
Procedure for Freezing mEPOC1. Freeze mouse EPOC cells when they reach > 95% confluence.
2. Warm Dulbecco’s PBS (without Ca2+ bath. Thaw EPC freezing medium at room temperature. and Mg2+) and 0.05% trypspin/EDTA in a 37°C water.
3. Remove EPOC growth medium, rinse mEPOC with Dulbecco’s PBS, and incubate the cells with trypsin/EDTA solution until approximately 90% of the cells begin to detach. Monitor the cells under a microscope to avoid over-trypsinization.
4. Add fetal bovine serum equal to 1/10 volume of the trypsin/EDTA solution to neutralize trypsin. Gently shake the culture vessel to mix.
5. Transfer the cell suspension into a 15ml conical tube. Take a small aliquot of the suspension to count cells. Centrifuge the cell suspension 250 x g for 5 minutes at room temperature.
6. Carefully remove the supernatant. Add a volume of EPOC freezing medium and resuspend cells to 1x10e6 per ml. Dispense 1ml into each cryovial.
7. Place cryovials in a freezing container to slowly lower the temperature in a -80°C freezer. Transfer the vials to liquid nitrogen the next day for long term storage.
Storage and StabilityStore at -20°C. Stable for 1 year from the date of receipt under proper storage condition.
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.


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