Hi, I am planning to sort animal cells (after perfusion) and fix them. Generally, I am collecting sorted cells in a buffer, centrifuge them and fix them using 70% ice-cold ethanol. I was wondering can I directly use paraformaldehyde for collecting FACS sorted cells. It saves my steps involved.

Please let me know if there is some protocol for that or someone has standardised this in their lab.

Best regards,

Ankur

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