I am working on dormant myeloma cells, so I am using dormant cells markers (antibodies) titration, I've prepared different dilutions 1:1, 1:2, 1:4, 1:8, then I stained myeloma cells with the markers, and tested by Aurora (flow cytometry). so I got an excel sheet with data including mean fluorescence intensity (MFI) for each marker

how do I calculate MFI to find the best dilution for my cells?

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