I am doing differentiation studies with hES cells. I have a whole experiment on one plate (no coverslips) but different time points to fix cells in certain wells for immunofluorescence staining. Is it possible to fix the cells with 4% PFA or 95% methanol and keep it in PBS while time course running for other cells in 37 degrees in incubator ?

Many Thanks for your response in advance, Reena

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