Good morning all and happy Friday!
My company provides testing on FFPE material, and we received paraffin blocks
and/or unstained slides and H&E stained slides. The blocks and H&E stained
slides are returned to the originating path lab after the results are generated
(currently 2-3 weeks after
Hi all,
I'm hoping someone from a vendor contact or someone who uses this can help. Our
quality practice requires us to receive and review CofA documents for all our
reagents. I'm having difficulty receiving them for Clarifier 1 which we
purchase through FisherScientific. The last one we receiv
Wait...what? When is Ventana p16 being discontinued?
Teri Johnson, HT(ASCP)QIHC
Manager, Clinical Trial Testing
T +1 760 516 5954
tejohn...@genoptix.com
Navigate BioPharma, Inc.
A Novartis Company
1890 Rutherford Rd.
Carlsbad, CA 92008
USA
Date: Wed, 5 Apr 2017 01:54:06 +
From: Samantha Cl
Hi Mariam,
Mayer's is a progressive hematoxylin. Therefore you should increase your time
in the stain to get a deeper color. You might try 10 or 20 minutes and see what
works best for you.
You can do your bluing in tap water or even buffer solution rather than
ammonium hydroxide if you prefer.
Dr. Richmond,
Thank you for all your contributions to the histonet over the years. I would
have loved working with you. I know I loved learning from you.
Best wishes and happy retirement!
Teri Johnson, HT(ASCP)QIHC
Manager, Clinical Trial Testing
T +1 760 516 5954
tejohn...@genoptix.com
Hi Bernice,
Likely there is something in your TUNEL procedure that is causing a problem
with histochemical nuclear staining. If it isn't the pre-treatment, it might be
the DAPI. After all, they do bind the same structures, and the DAPI might be
winning that competition.
Teri Johnson
Manager, C
Melissa wrote:
Good Morning, I am looking for feedback into technical bulletins and memos
recently released. We run benchmark ultras and special strainers. We are also
a facility that uses Vantage. We have never used the clear label overlays they
say are mandatory. I also do not like the sou
Hi Histoland,
I would love to hear from folks who are currently using the Primera slide
printers in your lab. We are working towards bringing them on line (networked)
and still have not worked out the physical bugs for printing and slide jamming.
We want to know some of the issues you have work
Anna wrote:
I'm curious as to why we heat the Auramine Rhodamine when we are staining
tissue sections but our Micro lab stains at room temp. It is because "it's
always been done that way"?
Thanks group,
Angie
Hi Anna,
If your dispensers are working properly, I would bet it's your slides. There
Dr. Rich Cartun asks: "What are people fixing testicular biopsies in to
evaluate infertility? In the past, I believe fixatives such as Zenker's and
Bouin's were used for this purpose since they enhance nuclear detail.
Obviously, those fixatives can no longer be used. Thank you."
I can unde
Hi Thomas,
Are you looking for true life expectancy or what is reported for depreciation?
In my experience, most tissue processors never die, but only need to be retired
due to lack of available support/parts or because a lab requires newer
technology.
Also in my experience, a "better" model c
Hi Histonetters,
Can someone tell me if they do anything specific to validate their IHC markers
on decalcified specimens? If no, do you test them anyway?
Teri Johnson
Manager, Clinical Trial Testing
Genoptix, Inc., a Novartis company
BioPharma
1811 Aston Avenue
Carlsbad, CA 92008
USA
Phone +1
Hi Charles,
If my memory serves, Clarifier 1 and Clarifier 2 are different mostly in that
one is an alcoholic solution and the other an aqueous one. So they both behave
differently in their mechanism of action. The alcohol based reagent should
remove more hematoxylin from the cells than the aqu
Hi Cassie,
I would strongly suspect your tap water. If you have a tap water rinse before
hematoxylin, the pH or treatment additives carrying over could be weakening
your stain. We fixed this problem previously by adding a bucket of DI water
between the tap water wash and the hematoxylin, and th
Hi James,
Nuclear bubbling artifact is most commonly seen in formalin fixed epithelial
cells, and GI biopsies are among those samples that are particularly
susceptible to it. It has been linked to inadequate fixation and also to
heating of slides prior to staining without complete air-drying of
As of January 2016, the updated NY State Dept of Health standards still require
received date, and date the material is placed in service or opened:
Reagents Sustaining Standard of Practice 4 (REAG S4): Inventory Control
There shall be an inventory control system for supplies. This system should
Hi Mohamed,
You didn't mention if you are doing human or animal histology. Since this is
only happening for kidney, I am wondering if what you describe is caused by the
kidney capsule? It might be preventing good infiltration of the fixative or
paraffin? I may be able to give a more precise ans
Maryann,
Whoa, bad day. I'm sorry for you and for the patient.
As for whether the testing usually performed in frozen section by Direct
ImmunoFluorescence can be successfully done on FFPE, Liz Chlipala is probably
the closest to answering this. This was likely a kidney or skin biopsy. The
pane
Dear colleagues,
We have an opening in our Clinical Trials Testing group, looking for an IHC
Specialist/Scientist. Here is the text:
Are you looking for a new opportunity with a reputable, fast-growing
organization? Do you want to find a place to work that has an exciting global
mission, inno
Hi Anna,
I really cannot beat what Tim has said in response to your concerns. He is spot
on and I think his experience in some way mirrors my own (with the exception of
industry experience).
My question to you, though, relates to your expectation. How quickly are you
expecting to advance in yo
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