From: Mario Roederer (ROEDERER@Beadle.Stanford.EDU)
Date: Thu Mar 24 1994 - 16:08:56 EST
We have approached the problem of autofluorescence from a different tack for a number of different applications: compensation. The fluorescence in a PE channel for unstained cells is reasonably well correlated with that in the FITC channel, especially for highly autofluorescent cells. Thus, by using the PE fluorescence to compensate FITC, one can essentially remove a majority of autofluorescence from the FITC channel. This improves sensitivity considerably (10x?) for measuring FITC fluorescences. References for doing this real-time (Alberti, Parks, and Herzenberg) and in software (Roederer and Murphy) can be found in Cytometry in 1986. mr
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