Hello everyone, I need help to understand how I can "co-cultivate" human platelets (derived from whole blood) with cancer cells. I have specific questions:

-How can I avoid platelets from clumping?

-How can I avoid platelets from stick to the bottom of the transwell plates I am using fot this co-culture system?

-Have someone worked already with apheresis platelets?

Thank you for your help!!

Giulia

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