We just purchased a Dako Autostainer and are in the process of figuring
out how to get rid of the haz waste that we will be generating. The
machine separates the haz from non-haz, thankfully. I've been
communicating with our waste facility and have been having some
difficulty. They want to know
We keep our DAB waste in a plastic container and give it to our waste disposal
company every 6 months.
No one has objected to this procedure.
Allen A. Smith, Ph.D.
Professor of Anatomy
Barry University School of Podiatric Medicine
Miami Shores, FL
-Original Message-
From:
Here's the website for consulting group we used: www.sprickstegall.com
Angie
Angela Bitting, HT(ASCP)
Technical Specialist, Histology
Geisinger Medical Center
100 N Academy Ave. MC 23-00
Danville, PA 17822
phone 570-214-9634
fax 570-271-5916
No trees were hurt in the sending of this email
We had ours analyzed by our Hazardous Waste Disposal Co. They provide
labels for the drums. We have a drum for the waste from the special
stains, the DAB waste, and the xylene waste from the recycler - labels
all provided by the disposal company. j
Joyce Weems
Pathology Manager
Saint Joseph's
We have a part-time dayshift and a full-time night shift opening for a HT. If
you're interested here's our web address.
www.geisinger.org
or call me directly.
Angie
Angela Bitting, HT(ASCP)
Technical Specialist, Histology
Geisinger Medical Center
100 N Academy Ave. MC 23-00
Danville, PA
Hello,
Does anyone have experience using PGDFR in canines and if so, is
there a canine species control that is known to react with PGDFR?
Thank you,
Sandy
Sandra Cheasty
Histology Supervisor
UW-Madison
School of Veterinary Medicine
608 263-1680
just wanting to see what everyone's favorite xylene substitute is for clearing
slides before coverslipping??
Gene
Cleveland Clinic
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We use Formula 83 ... we have had no problems in all phases.
Gary
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
njoydo...@aol.com
Sent: Wednesday, May 13, 2009 7:25 AM
To:
N-butyl acetate aka butyl ethanoate.
njoydo...@aol.com wrote:
just wanting to see what everyone's favorite xylene substitute is for clearing slides before coverslipping??
Gene
Cleveland Clinic
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I second Gary's comments. We use Formula 83 in all phases also.
Linda
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Martin, Gary
Sent: Wednesday, May 13, 2009 10:50 AM
To: njoydo...@aol.com;
Does anyone have protocols for doing histology and hematology on blood
spots?
Helen Johnson (he...@health.state.ny.us)
IMPORTANT NOTICE: This e-mail and any attachments may contain confidential or
sensitive information which is, or may be, legally privileged or otherwise
protected by law
We use Propar by Anatech. It works great.
Lynette
njoydo...@aol.com 05/13/09 10:25 AM
just wanting to see what everyone's favorite xylene substitute is for
clearing slides before coverslipping??
Gene
Cleveland Clinic
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tulane !!!
2009-05-13
TF
发件人: Lynette Pavelich
发送时间: 2009-05-13 23:49:59
收件人: njoydo...@aol.com; Histonet@lists.utsouthwestern.edu
抄送:
主题: Re: [Histonet] xylene substitues
We use Propar by Anatech. It works great.
Lynette
njoydo...@aol.com 05/13/09 10:25 AM
just wanting to see
My recipe for 0.2M borate acid is:
Sodium Borate acid.10 H2O (molecular weight 381.42, Na4B4O4.10H2O)
19.07 gram
H2O
1 Litre
Adjust pH = 7.0 with 5M HCl
Is this fine?
2009-05-11
good morning,
Is there anyone out there who has eliminated using Peroxidase Block on
either IHC or ICC?
Thanks,
Gene
Cleveland Clinic
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We detoxify our DAB using this method from: HAZARDOUS MATERIALS IN THE
HISTOPATHOLOGY LABORATORY, by Dapson Dapson, fourth edition, pg 184.
1. Prepare the following aqeous stock solutions:
a. 0.2M potassium permanganate (3.16% or 31.6g KMnO4/liter)
b. 2.0M sulfuric acid (11.2% or 112 mL
Have any of you tried the Dab/Out? It is a system that extracts DAB from
liquid waste. The liquid passes through a cartridge and captures the DAB,
then you can dispose cartridge as a dry solid waste and pour the rest of the
liquid down the drain. It is known to be cost effective and
We were told that, in Miami-Dade County, we would have to apply for a license
to do this. We gave up on the cumbersome licensing procedure.
Allen A. Smith, Ph.D.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On
Hello Histonetters
My Immuno lead tech has left and I urgently need a replacement
Its a full-time position and requires good IHC experience as well as routine
Histo experience - an all-rounder
Need someone with at least 7-10 years experience as its a Senior post
Anyone interested?
Send me your CVs
Hi All,
I am looking for part-time Histology work in Phoenix AZ. I am available for
almost any shift, my current employer is very flexible with my hours. I have
been in field for 17 years and know all aspects of Histology. Please respond to
this email if you have any questions.
Thanks!!!
Is anyone working on CD11c in murine tissues? If so, can we exchange
emails? ... I have some questions.
Andrea Hooper
anh2...@med.cornell.edu
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Anyone working with CD115 in mouse? If so, may I contact you as I
have a few questions?
Andrea Hooper
anh2006 @ med.cornell.edu
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Fellow Histonetters,
The Louisiana Society for Histotechnology is pleased to announce
the 26th Annual Symposium/Convention:
Your
Histeaux Surplus Package
June 12 13, 2009
Hello everyone,
We have decided to purchase a refurbished Leica cryostat and are trying
to decide which model to choose; does anyone have experience with the
1510, the CM 1800 or the 1800? Any feedback would be appreciated.
Thanks!
Janet
___
We have an 1850 and like very much, but see if you can find one with the
ultra violet light for sterilization. It would save a lot of hassle.
Gary
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Dertien,
I have always liked a very simple method from an older edition of
Humanson's book.
1. Bring paraffin sections to water.
2. Stain in 0.1% Toluidine Blue in distilled water, 2-5 minutes
3. Rinse thoroughly in distilled water.
4. Dehydrate in 2 changes of acetone, 5 minutes each. Dehydrating in
I'm sending this for a researcher here. He's got a lot of tissue in storage
that's still 'wet' (still in various fixatives and bagged up). The tissues
have been in fixative for over 10 years. He wants to know if he can still hang
onto the tissue for future IHC use, or has it been in fixative
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