What species is the kidney you are trying to stain with IHC. Because you
mentioned that you used normal human kidney and it worked , but Rhesus kidney
didn't stain. I'm wondering if the Rhesus kidney is human or another animal
species? The Novocastra CD34 (QBEND10) is intended for human tissue.
Gareth
I would think it would have more to do with OSHA than CDC - this could involve
several modules.
We have modules that cover the following - this is not all that we train on.
If you are a small business OSHA can help out. We have utilized their services
with a voluntary compliance
Hi Gareth,
You will probably have to design your own Continuing Education Session.
I would recommend the following topics:
1. Nature of formaldehyde - safety aspects, explanation of the MSDS.
2. What formaldehyde is used for
3. Appropriate packaging of pots containing specimens in
Okay, is there a training course for just transportion formalin fixed
specimens. CAP told me last year that anyone picking up specimens for us
has to go through a training course. The inspector seemed to be more
concerned with the employees knowledge of formalin and possible spills.
So, does
2 more bits of information about my dilemma;
I did try staining without any retrieval - no signal
I am using rhesus kidney as a control (getting no signal), but I also ran some
human kidney and got beautiful staining with a 20 minute HIER using a pH 8 EDTA
buffer.
So I know the antibodies and my
Hi Cathy,
EDTA (Retrieval #2) for 20 minutes on the Bond-Rx should be sufficient. And all
that is necessary. Please contact me if you need additional help.
Best,
Eddie Martin, HTL, QIHC
edmarti...@gmail.com
Sent from my iPhone
> On Jun 29, 2016, at 8:16 AM, Cathy M. Mathis/Comparative
Hi All-
I have a couple things I am looking for assist on today:
1. Are your HT's doing frozen section cutting? Are they also doing the
frozen section gross and inking? Are they staining the slides? We are
interested in doing this and looking for how others do.
2. Do your HT's
Hi Histonetters --
I need a short term histologist (registered) for a three week stint in Texas.
GOOD lab, I'd go do it but the schedule doesn't line up for me :(
Everything paid-- please respond via email with your resume.
Starts July 11--
Holler!
ad...@fullstaff.org
Cheryl Cheryl Kerry,
Hi Gabrielle,
Are you doing floating sections? Did you cut the tissue recently? Do you
notice your tissue is also "sticky"? If you do, there is a possibility that
the tissue may be infected by bacteria. Try washing the tissue with PBS or
TBS with 0.1% sodium azide a couple time. Sometimes it
Sorry about hitting send too soon.
Repeat of things to try:
a. Do not use regressive hematoxylin and eosin where hematoxylin
can be overly differentiated i.e. removed from too thin sections. Use
progressive hematoxylin i.e. Gill II or Gill III type formulation. DO NOT
use acid
You wrote:
When I cut at 2μm my H and special stains look pale. How can I get my
stains to pop or am I stuck with pale looking stains when sectioning that
thin?
I run manual specials and a manual regressive H For H I've tried
increasing my time in hematoxylin (beyond the manufacturer
Angela:"Pale" results are the trade-off for great quality very thin "2 µm"
sections but you can always improve intensity somewhat .1- your "regressive"
stain, if it is "modern Harris" has the inherent problem of lacking mercury
chloride and it is little you can do about. Perhaps if you use
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
Richard,
You wrote: 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.
Hi Histonetters!
Have a safe and Happy July 4th Weekend.
I Have A Fun Idea to Share for Pool Parties and Cookouts
Sprinkle Red Pop Rocks And Blue Sprinkles On Iced Sugar Cookies To Make
Edible Firecrackers!!
I guarantee you will be the hit of your Independence Day Celebration!
Do you have any
To whom it may concern,
I am a undergraduate researcher at Vassar College. I am performing
immunohistochemistry on mice using Arc primary, anti-mouse biotinylated IgG
(1:200),ABC (Vector labs) and DAB. So far we have gotten really great
staining, however the last immuno I ran, the sections, once
Good morning my fellow Histo-netters,
Does anyone have experience with any CD34 antibody that would work in FFPE
rhesus tissues? A few companies have one with clone QEBend 10 and say that it
works but I have had no luck. I am using the Bond RX polymer system and I've
tried all the epitope
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