We are attempting to optimize the procedure to label transfection along with cell cycle in HeLa cells. So far we have co-transfected with CD20 and then labeled the surface with CD20-FITC. We found 5-13% CD20 positive with good PI patterns after the usual 70% ethanol fixation. We used the same cells and fixation procedure with GFP as the reporter and hoped to find similar results. Unfortunately, there were few cells GFP positive and what may be there are of very low intensity, barely over background. We are looking for suggestions for improving our GFP and keeping good PI patterns. The GFP is from Invitrogen and they have been somewhat helpful, but have not done this with PI. Is fixation causing a problem?? If so, is there a better procedure which will permeabilize and fix to get both GFP and PI to work?? Ultimately, we want this to work in some fibroblast lines, but HeLa is our control. Thanks in advance for any hints. Wendy Schober wschober@bcm.tmc.edu
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