The KMnO4/oxalic acid sequence will weaken the tissue adherence.
If you do not have to use Peroxidase/DAB, then I would recommend alkaline
phosphatase labelling (+red chromagen).
Remember KMnO4/oxalic acid can be deleterious to some antigen-antibody
reactions.
We found that LCA, CAM5.2, L26,
Yep,
We do.
We have a separate dehydration sequence for PAP and other special stains
(separate from the eosin dehydration sequence).
We have a Leica (used to be Vision Biosystems) Autostainer
Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Principal Scientist, the
I am getting a bubbly artifact on my tissue due to the OCT not being washed off
the slide after putting it on a cryojane slide and flashing it and staining
with H Is there a trick to dissolve the OCT away
Sent from my iPhone
___
Histonet mailing list
Cool trick Jeffrey!
On Tue, May 10, 2016 at 12:14 PM, Maxim Peshkov via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Karen,
> The bleaching reagents will not compatible before IHC anyway.
> Some tips:
> 1. Do IHC-test as usual and counterstain nuclei with methylene blue
> Loeffler at
Does anyone know of a supplier for P24 control slides?
Sent from my iPhone
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
There is a fantastic resource for antibody assessment and optimization and they
have done p16 as well as many many other antibodies. Their results of testing
is free on line. p16 is http://www.nordiqc.org/Epitopes/p16/p16.htm from 2009
with many different companies antibodies.
Here is the
Karen,
The bleaching reagents will not compatible before IHC anyway.
Some tips:
1. Do IHC-test as usual and counterstain nuclei with methylene blue Loeffler at
3-5 sec, only for
profile of chromatine. The melanin will stain at green color.
2. Use any red color chromogen for IHC. It will be some
Hi-
Job Opening:
OSU Histology Lab, LLC
Columbus, Ohio
Assistant Laboratory Manager for a small reference based laboratory. Simple
grossing and histology are performed.
Musts:
Graduate of a school of histology with a HT/HTL certification or equivalent.
A minimum of an associate's degree in a
Mary,
We run both protocols on the same stainer, however, each protocol has it own
set of reagents except for the common water wells and the two xylenes at the
end before the final xylene. We have the Leica ST 5020, which has 36 wells not
including the 2 oven wells.
Hope this helps.
This is the CAP regulation that talks about cross contamination.
CYP.04150 Cross-Contamination Phase I
There is a written procedure to prevent cross-contamination of specimens during
processing and staining.
NOTE: Procedures must prevent cross-contamination between gynecologic and
Hey Mary,
The problem is not the machine, it is the reagents sharing that is the issue.
You can use different reagents and protocols for the Histo and Cyto slides and
on the same instrument. You might even get away with changing your Alcohols
and filtering everything else and see how that
You are right. Bleaching is a "rough" procedure for the "survival" of sections
and if on top of that you left the section overnight in DiH2O that is a recipe
for disaster, as the one you experienced. Try to do the whole procedure during
the same day.Additionally it seems to me that 6h in
Hi Karen- I have also had problems getting tissue being stained for IHC
markers to adhere to the slide. The Potassium permanganate is really harse on
the tissue (if you can get the sections to stay on). Here is a trick I picked
up at an NSH lecture that I have used successfully several
Good Morning,
I need some help. Yesterday I bleached some heavily pigmented tissue. I have
to run some IHC's on them. I bought the bleaching kit from American Master
Tech. I had to put the Permanganate for about 6 hours to get the melanin and
then a couple of minutes in Oxalic Acid. I had
Hello,
I have a Full Time/Permanent job opening for an ASCP certified Pathologist
Assistant in Ohio. Please contact me for details. Have a great day!
Melissa Owens
President, Laboratory Staffing
Allied Search Partners
T: 888.388.7571 ext. 102
F: 888.388.7572
I would be concerned with potential cross-contamination. In my lab we had 2
staining instruments, one for cytology and other for histology.René
On Tuesday, May 10, 2016 10:59 AM, "Mullen, Mary via Histonet"
wrote:
Hello all,
I work in a small, low
Has anyone found a way to do p16 staining without purchasing anything from
Ventana?
My company wants to do P16 but refuses to by any ventana products and I
have explained it is a waste of money to keep testing the antibodies from
all the other companies.
--
Charles Riley HT(ASCP)CM
17 matches
Mail list logo