Hi histonetters,
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.
Wendy

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