I am wondering if I should fix and permeabilize my cells with a 50:50 mixture of ice cold methanol and acetone when I perform transwell migration assays. I have seen most methods mention using just cold methanol. I am wondering what the difference is. Also what is the optimum amount/volume of matrigel to use for invasion assays? I work with HCT116 and SW620 colorectal cancer cells.

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