[Histonet] culture cells
|From:||Jose Luis Palazon Fernandez |
maybe you can use trypsine to detach the cells, wash the trypsine out with serum or culture media and them concentrate the cells by centrifugating. After you obtain a concentrated suspention you can drop the cells on the slides using a Pasteur pipete, let them dry and fix with formalin or alcohol, and then treat as a conventional slide for H&E.
hope this help
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