Good morning,
I am hiring for several permanent positions with a growing
medical diagnostic company here in Central New Jersey. My client has
several IMMEDIATE openings for Histology Technicians who have experience
with Gram Staining, Section Cutting and Paraffin Embedding. Hands-on
Good morning,
Is it possible to decolorize MMA slides?
Thanks,
Betsy
Betsy Molinari HT(ASCP)
Texas Heart Institute
Cardiovascular Pathology
6770 Bertner Ave
MC1-283
Houston,TX 77030-2607
832-355-6524
832-355-6812
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Histonet mailing
Do you mean deplasticize, as in remove the resin? If that is what you mean,
yes, you can remove mma with xylene, you cannot remove GMA.
Patsy
Patsy Ruegg, HT(ASCP)QIHC
IHCtech
12635 Montview Blvd. Ste.215
Aurora, CO 80045
720-859-4060
fax 720-859-4110
www.ihctech.net
www.ihcrg.org
If you want to remove the MMA you can also use 2-Methoxyethyl Acetate or
Acetone. If you want to decolorize like a hematoxylin, yes you can do that
also.
Frances L. Swain HT(ASCP) A. A. S.
Special Procedures Technician
Department of Orthopaedic Surgery
Center for Orthopaedic Research
Barton
I hate to beat a dead horse.but how do you handle non-certified grossing
staff.? They all meet the CLIA guidelines, but are they allowed to gross in the
evening without the presence of a technical supervisor?
And how do you handle salaries for those that process and those that
Define presence? If they are able to have access a technical supervisor or a
Pathologist if they have a question then this may just cover it. We have a
Pathologist on call that can be in within minutes if there are any
questions.
On Mon, Mar 16, 2009 at 10:55 AM, godsgal...@aol.com wrote:
I
Good morning everyone
We are starting a rather large project and I would like to get some input as to
the best version of antibodies to the following antigens-what are people using
for the following and where do you get them from. This will be either frozen
sections or formalin fixed paraffin
From my point of view, shared by all AP and many managers, the answer is NO,
they cannot, and should not. Histology samples are too precious to be handled
by somebody without the proper training.
René J.
--- On Mon, 3/16/09, godsgal...@aol.com godsgal...@aol.com wrote:
From: godsgal...@aol.com
René, my friend
This is my opinion as well and I have stated so, but is there any documentation?
Roxanne
-Original Message-
From: Rene J Buesa rjbu...@yahoo.com
To: histonet@lists.utsouthwestern.edu; godsgal...@aol.com
Sent: Mon, 16 Mar 2009 11:24 am
Subject: Re: [Histonet]
Hi all,
I'm trying to use Tweak R (Fn14) on mouse lung. I've got a rabbit
polyclonal from abcam that supposedly is validated for IHC-paraffin -
have tried it with and without HIER (citrate) and with and without
detergents - was worried that as its a transmembrane protein maybe I was
washing
I am in a research lab and we are currently testing automated IHC
machines. A couple months ago we had the Bond Max from Leica. The
machine gave me nothing but problems. They said it was because it was a
demo unit and the real one would not do that (who knows). The
interesting thing, though, was
Patsy I have a couple of questions for you but have the wrong address.
Margaret Perry
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Hello Histonetters!
I hope everyone had a great weekend. I wanted to follow up in reference to a
full time, direct hire position for a histotechnologist in Boston. My
company offers a referral bonus up to $1000 paid to you if your referral is
hired. Forward this to anyone you feel fit.
If
Actually, as long as they meet the standards for High Complexity testing they
can gross...according to CAP you have to have no knowledge of anatomy to
process.
Roxanne
-Original Message-
From: Histonet Alias histonetal...@gmail.com
To: godsgal...@aol.com
Cc:
According to CLIA, the employee who grosses must also possess a state
license when working in a state that requires licensure, such as Florida.
Keep in mind that CAP rules do not apply for those laboratories that are not
CAP accredited.
Exert from CLIA -
In order to qualify as high
Hello,
I was asked to do BrdU immunostain on rat brain tissue. Does anyone have
experience of it?
1.Do you prefer frozen or paraffin?
2.Which antibody you recommend?
3. If 35um frozen is requied, what thickness you will use if you want go for
paraffin?
Thanks,
Amy
Fellow Histonetters - I am looking for feedback on the alternative methods
to prepare Non GYN cellblocks. We currently use the Fix Sediment Method
where you spin the fluid to achieve a button, pour off the supernatant, and
pour formalin onto the button to harden it. What do others do? Does
hi, we worked a lot on this.
I prefer to use 40 um frozen sections.
Abcam anti-BrdU (rat sourced) is the best ever I know. It does not have high
background with rat IgG. Some other mouse-/sheep- sourced BrdU are available.
2009-03-17
TF
发件人： Amy Lee
发送时间： 2009-03-17 05:02:28
收件人：
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