Hi Alice, We currently are using only one QDOT with our 407nm laser on the CyAn as we have commercially available, and cheaper, fluorochromes in the other 8 channels. We use the streptavidin conjugate and a biotin conjugated primary. Randy T. Fischer, NIH/NIAMS B Cell Biology Group 9000 Rockville Pike Bldg 10, Room 6D50 Bethesda, MD 20892 (301) 594-3537 (voice) (301) 402-2209 (fax) > From: "Alice L. Givan" <Alice.L.Givan@Dartmouth.EDU> > Date: 14 Apr 2006 16:10:08 EDT > To: Cytometry Mailing List <cytometry@flowcyt.cyto.purdue.edu> > Subject: Quantum Dots > > Hello, > Can people tell me how you are staining cells with antibodies and the Quantum > Dot > fluorochromes? Are you conjugating the dyes to the antibodies yourselves > (using reagents > from where)? Or are you limiting yourselves to one Quantum Dot color with the > biotin/streptavidin combination? Or are you using different animal-derived > antibodies > with animal-specific secondary antibodies (from where)? Or what am I > missing? The goal > is to use lots of QDot colors with just 407nm excitation -- but I don't know > how close we > are to being able to do this. > > Thanks. > > Alice > > Alice L. Givan > Englert Cell Analysis Laboratory > of the Norris Cotton Cancer Center > Dartmouth Medical School > Lebanon, NH 03756 USA > tel 603-650-7661 > fax 603-650-6130 > givan@dartmouth.edu > www.dartmouth.edu/~celllabReceived on Tue Apr 18 11:38:00 2006
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