[Histonet] theoretical question on fixing and section
(formalin and cryosections)
Gayle Callis
gcallis <@t> montana.edu
Fri Jul 30 12:46:06 CDT 2004
"Right?" Not necessarily. Many people do unfixed bone frozen sections (
not fixed nor decalcified) and sectioned using the Tape Transfer Cryojane
system, Instrumedics. Some antigens hold up well with formalin fixation
and decalcification followed by paraffin processing. It will depend on
what you want to see. It is always advisable to use gentle
decalcification, buffered formic acid or EDTA, but there are decalcified
bone retrieval kits, Biogenex has one, to help counter the effects of
decalcification. Doing retrieval on frozen sections is sometimes difficult
with section loss.
Remember that if an acid decalcifier can compromises the antigen EDTA is a
good choice, followed by paraffin processing.
There are excellent review publications on the effects of decalcification
on bone immunohistochemistry. This is also true of the effects of fixation
on antigens. If you fix, decalcify and want to snap freeze, the acid would
have to be rinsed out of bone, and the decalcified bone would need sucrose
cryoprotection. There are methods that fix, decalcify with bone snap
frozen, for IHC. Go to J Histochemstry and Cytochemistry, look up Kim
Kusser as the author. It is not a SHORT method, time consuming if one has
to do more rapid diagnositic work.
At 11:22 AM 7/30/2004, you wrote:
>Hello all,
>
>This question refers to bone tissue. If you want to do IHC, cryosections
>generally give better results, right? Does it make sense to fix the tissue
>in 10% formalin, decalcify (say in formic acid), and then "embed" in OCT and
>freeze in dry ice to take cryosections? It just seems like people do 10%
>formalin and follow that with paraffin embedding..
>
>Thanks!
>
>Zarana Patel
>degaboh <@t> rice.edu
>
>
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Gayle Callis
MT,HT,HTL(ASCP)
Research Histopathology Supervisor
Veterinary Molecular Biology
Montana State University - Bozeman
PO Box 173610
Bozeman MT 59717-3610
406 994-6367 (lab with voice mail)
406 994-4303 (FAX)
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