Dear Histonetters,
I recently replied to a question about staining extracellular ground
substance with alcian blue. Here is some more information.
With the alcian blue-PAS sequence it is necessary to have a good alcian blue
dye - the same as or functionally equivalent to the original alcian
Anyone out there having any issues with the Ventana LCS?
When you are cover slipping are you seeing any water/residual LCS on the slides?
I was wondering if we should dry our slides before cover slipping instead of
running
them down? Any information would be greatly appreciated!
Brandy Burnett
Kristie,
For heart you could try the elastic Trichrome, it will stain the ground
substances and is faster than the Movat. If your ground substance is devoid of
staining it could be the phosphotungstic acid. Is it 5%, and fresh? Are you
using two changes at 5 min each? Continue with the
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Hi,
I hope you guys are doing well. I am looking for a job opportunity in Canada
and I will really appreciate it if you guys could help me.
I am an Histotech. With both HT(ASCP)and HTL(ASCP)Certifications. I also have
both QIHC(ASCP) and QLS(ASCP)Qualifications.
Thanks,
Isaac
Could you please let me know what % of Ammonia water is used for distain Masson
Trichrome?
Or what % is most common used?
Thank you.
Lin S. Bustamante, B.S., H.T.(ASCP)
VIBS Histology Laboratory Supervisor
College Of Veterinary Medicine
Texas AM University
College Station, Texas 77843-4458
You certainly can air/oven dry your slides instead of running them down and
coverslipping; we do that with the slides we take off in the morning when we
get in. As to your problem with water/oil on your slides, something is not
right in your dawn water rinsing, dehydration and/or clearing
Usually the strong 28% is used but I always prefer using a diluted solution
so I have more control on the distaining.René
On Thursday, July 2, 2015 12:10 PM, Bustamante, Lin
lbustama...@cvm.tamu.edu wrote:
Could you please let me know what % of Ammonia water is used for distain
Is anyone able to recommend a good reference on preparation techniques for
immunostaining of cytologic and frozen specimens? I'm studying for the qIHC
exam and I'm striking out with my usual sources (Carson, DAKO guide, etc.) on
some of the more specific questions in these areas.
Thanks!
Anna
I have had an issue on a couple of occasions now. Our lab gets really
humid and when I have a block that needs re-embedded, the tissue becomes
saturated with water and difficult to cut. The tissue seemed properly
processed before, but after embedding, it almost peels out of the block.
Has
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