We recently received samples prepared from solid tumors for intracellular nuclear antigen staining. Because there were a lot of damages to the cells and the samples are not suitable for flow analysis. What can we do to salvage these samples? Or, alternatively, what technique is recommended for dissociation of solid tumors in general for future study. We have access to Current Protocols in Cytometry. Can someone comment on those techniques. Thank you for your help in advance. Cindy Zhang Senior Scientist GlaxoSmithKline Cellular Pathology Safety Assessment Tel: 610 270 4722 Fax: 610 270 7202
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