Labeled Virus

Dennis_Young@CIS.ucsd.edu
Wed, 7 Feb 1996 10:30:00 -0800

Is there a better way to follow virus binding than R-18 "dequenching"
(Leary,JF, Notter,MFD, Kinetics of Virus Adsorption to Single Cells Using
Fluorescent Membrane Probes and Multiparameter Flow Cytometry, Cell Biophysics,
4, 63-76, 1982.)?
Our first attempt failed to see any rhodamine fluorescence. What would be a
good positive control?
FACSTAR+, 514 nm excitation, 560 dichroic and 600 SHORTPASS in FL-2.

Dennis
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* Dennis J. Young Voice : (619) 822-0407 *
* Flow Cytometry Core Facility FAX : (619) 822-0412 *
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