I am trying to use BODIPY on cultured B cells and then analyze using flow cytometry. However, I will have close to 80 samples in a 96 well plate and am afraid that the fluorescence shift will be significantly different as a function of when the samples are run (i.e. more shift in the later wells). I have been looking for ways to slow or halt the reaction since BODIPY is not fixable, but have not found much. Any advice from those familiar with BODIPY protocols? Thanks!

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