I am going to receive a few samples that I never done before. I hope you can
help me. They are fibroblast cells cultured in recombinant collagen sponges.
They are now fixed in 4% formalin (sponges and cells that hold in). I need
to process these sponges and read cells after H&E staining. Any body could
tell me how should I process these samples so that cells will not get lost
afterwards and good morphology is kept?
Thanks for any suggestion.
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