Since we're talking buffers , I was wondering what experience
folks have had using commercial buffers in sorters. I'm interested
in cell viability, growth characteristics after sorting,etc. We've
always used sterile PBS - any other inexpensive alternatives?
Peter
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Peter A. Lopez (617)632-3179 (voice)
Dana Farber Cancer Institute (617)632-3139 (voice)
Core Flow Cytometry Facility NO FAX!
44 Binney St. Room J-312
Boston,MA 02115 PLOPEZ@sorter.dfci.harvard.edu
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