Do I have to use a very strong permeabilization protocol if I want to stain intracellular antigens with QDots? I tried to stain MHCII in and on murine (not fully matured) DC and visiualized them on the confocal. Compared to FITC I get a brighter extracellular fluorescence with QDots (525), but with the FITC antibody I can see a bright signal inside the cell, which is totally absent with QDots. For permeabilization I used Triton-X, counterstained with DAPI and Phalloidin Alx594. Many thanks MaxReceived on Mon Mar 7 14:38:00 2005
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