Is there a CAP or some Regulation with a percentage for correlating the frozen
section diagnosis with the final diagnosis, my pathologist seems to think there
is we are joint commision and can't find anything about this, can anyone help??
Thanks
Histology/Cytology Supervisor
S. Kathy Baldwin,
Hello Everyone,
Does anyone have any suggestions for cutting corneal rat brains (20 microns),
fixed in PFA, treated with sucrose and embedded into OCT. They cut well but
when I pick them up on the slide they always have wrinkles, I have tried many
different things with no luck.
Different modes
I have been asked by a new pathologist to look into a DAB enhancer for use on
our Bond III instruments. Are many of you using this on the Bond, or any
other staining platform and what are the pros and cons of its use?
Thanks!
Martha Ward, MT (ASCP) QIHC
Manager
Molecular Diagnostics Lab
Sorry but I cannot get my messages to go through to the Histonet so I am
piggybacking onto a previous message:
I have been asked by a new pathologist to look into a DAB enhancer for use on
our Bond III instruments. Are many of you using this on the Bond, or any
other staining platform and
Hello to Everyone,
Does anyone have an antibody for iNOS that will work in Human? I appreciate any
help you wonderful people could give me. Also, could you share your protocol
with me?
Thanks,
Pat
Pat Bell HT(ASCP)
Medical Oncology
University of Colorado, Denver
12801 E 17th Ave, MS 8117
I don't know why anyone would want to use a DAB enhancer for slides prepared on
Leica-Microsystems' Bond Max platforms. The resulting immunoreactivity is
exceptionally Robust in my experience when using their Bond Polymer Refine
Detection kit. Could this request be for a protein target
I am way out of my league here and need help from the histonet world. I have
been asked to do wet and dry silver nitrate-protargol staining for a research
project on ciliated protozoa. I need to speak with someone out there who has
done this before. You may contact me directly.
Thanks
Hi Margaret,
One possible solution to the wrinkling problem you have is to float your twenty
microns onto the slide. I do this regularly with mouse or rat brain by cutting
the section and putting it into culture wells with buffer solution. Then once I
have completed my sectioning I lift the