From: tony_ward@bdis.com
Date: Tue Jun 06 1995 - 12:32:12 EST
Regarding the uppersize limit of a scan: The cuvette is 180 x 80 micron. I wouldn't try anything bigger than 70 micron, it's asking for trouble. Note this is especially true for beads - cells obviously are more flexible and might actually go higher than 80 micron. You might try running your mixture of bead / cells through a known pore size filter/mesh prior to analysis and go from there. The fluorescence is indepedent. Regards Tony Ward Assoc Product Manager BDIS
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