Re: Cutting fixed brains at 20 microns
|From:||Suzanne Pham <Phams@omrf.ouhsc.edu>|
I have been perfusing mouse brains with 4% paraformaldehyde, soaking
overnight in a 30% sucrose/PBS solution, and then cutting frozen, 20-25
micron sections on a sliding microtome for some time now. It's a fairly
simple method, but there has been the problem of freezing artifact
developing in the tissue, causing holes to form. I've been experimenting
with a few different conditions to try to get tissue with better morphology
(i.e. no holes at all) and to date, have found that after perfusion,
soaking in a 50% OCT/PBS solution overnight has given me the best results.
The morphology looks better than anything I've gotten with the sucrose
immersion. I know a lot of people use the sucrose method and I'd like to
know if they get the same holes as I do in their tissues.
Oklahoma Medical Research Foundation
We are asked to cut 20 micron sections of rat brains perfused in a
>paraformaldehyde fixative. Can you experts out there suggest ways of doing
>this. I know of adding sucrose to tissue and doing frozen sections. Which
>may be very difficult. The equipment we have is a tissue tech cryostat and
>rotary microtomes. Thanks in advance for your help.
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