Dr. J.Ostwald ENT-Clinic University Rostock Dear flowers, I want to stain bad looking cells, growing (I hope so, because I can not see the cells with phasecontrast or Hoffmanns modulation contrast) in a 3-dimensional meshwork of collagen.Would anyone know of a good method to stain the cells in culture, thereafter beeing visible in normal light microscope or UV-excited (with fluorochromes) and staying alive, if possible. Thanks for help
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