|From:||Jocelyn Torcolini |
I have a few questions about cryostat sectioning.
In what situations is a cryostat better than regular paraffin processing, and why?
How do you get cryostat sections to stick to a slide for staining?
Do you need to fix tissue for cryostat in paraformaldhyde/sucrose solution? Can you section fresh/frozen tissue?
Thanks in advance,
Electron Microscopy Facility
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