I just tried fluo4/fura red for the first time and I saw a lot of crossover of the the fluo4 into the fura red channel. About a 10X increase over unstained cells. As all FACSCalibur users know, there is no way to directly compensate FL3-FL1, so what now? Is this just a matter of them adding way too much fluo4? I'm open for suggestions. David McFarland Howard Hughes Medical Institute Flow Cytometry Facility Vanderbilt University Medical Center
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