[Histonet] improper fixation
|From:||"Kristopher Kalleberg" |
Last week I was unable to collect 18 biopsies 2mm biopsies for a clinical that
is being run and had a colleague collect them for me. After running routine
H&E and Fontana Mason stains I found that two biopsies were improperly fixed.
Since I have never had this problem before, I was wondering if it is possible
to run the sample backwards through paraffin, xylenes, and alcohols and then
fix the samples again in 10% NBF and reprocess to paraffin. If this is
possible doe sanyone have a protocol or know what the effects will be by doing
this? Thank you in advance.
Histonet mailing list
<< Previous Message | Next Message >>