All, I am working with a transformed endothelial cell line. I have to culture them to confluency before checking their fluorescence by FACS. When I use trypsin/EDTA the cells come off nicely, but they remain in large "sheets" that do not come apart with pipetting as many cells will. Does anyone have any suggestions as to how to disaggragate these sheets of cells? Thanks, Mike -- _____________________________________________________ / Michael J. Herron, U of MN, Dept. of Entomology / / herro001@umn.edu / / 612-624-3212 (lab) St. Paul, MN 55108 / /____________________________________________________/
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