5% Formic Acid
Thanks
Lee Ann
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lewis, Patrick
Sent: Friday, October 22, 2010 4:06 PM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Recommendations
Great opportunity for a Histotechnician in a brand new laboratory!
Bellmeade Dermatology in Nashville, TN is looking for a certified HT or
HTL to run their newly constructed laboratory. Bellmeade Dermatology has
been in the dermatology business for 18 years with 3 physicians and 2
Nurse
We wear gloves we have to sterile section blocks for DNA/RNA extraction.
Keeps the slides free from contamination if we are placing sections on
slides, otherwise we are sticking them in a vial. All equipment associated
with the sterile sectioning is cleaned between each block (block holder,
blade
Hi everyone,
Does anyone know of a source for packaging exclusive to mailing paraffin
blocks? Vendors please feel free to reply as well.
Thanks!
Jeanine Bartlett, BS, HT(ASCP)QIHC
Centers for Disease Control and Prevention
Infectious Diseases Pathology Branch
1600 Clifton Road, MS/G-32
Hi Jeanine,
At the NSH vendors I got a sample of a neat clear plastic holder from Source
Medical Products, www.sourcemp.com, 1866-735-9965, holds 4 maybe 8 blocks for
mailing, depending upon the thickness.
Shirley
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Hi Histonetters!
I am back with some questions on protocols for microwave processing. We
have the Milestone processor. For any of you out there who use the
Milestone, do you find the pre-programmed processing runs reasonable for
your use or have you modified them? If modified, would you be
GNF is currently seeking a temporary Scientific Associate to join the Histology
group, for the beginning of March 2011 through the end of July 2011. Perform
necropsies, tissue processing, slide sectioning, routine staining, special
staining, immunohistochemical staining and complex procedures
From: Hannen, Valerie
Sent: Monday, October 25, 2010 11:39 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Saponin Technique
Hi folks..
I am hoping someone out there in Histo-land can help. One of our
Pathologists is asking us to check into doing the
It's been a while but I think that we used to add a little diluted glacial
acetic acid to our cytology specimens to lyse the red cells.
Not sure on the dilution, but maybe someone else knows.
Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of
I don't know about the procedure you have but ours only uses a 1% solution of
saponin, a 3% solution of calcium gluconate, and a balanced salt solution. We
get the balanced salt solution from our pharmacy.
Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740)
Lots of blood can be a problem in cyto specimens, especially smears. If
you are making smears from fresh specimens in particular you may elute
the obscuring hemoglobin by dipping the smear directly in acid alcohol
(i think 5% hcl-95% etoh). We do this frequently for CT guided FNA's
(particularly
Hi Histonetters,
I was wondering if any one could tell me where can I find a human brain amyloid
control. I just need some suggestions on where to order them ( control slides)
from. Please feel free to list any suggestions.
Thanks
___
-- Forwarded message --
From: Brandi Higgins brandihigg...@gmail.com
Date: Mon, Oct 25, 2010 at 12:08 PM
Subject: Re: [Histonet] FW: Saponin Technique
To: Hannen, Valerie valerie.han...@parrishmed.com
We use Carnoy's to lyse the red blood cells. We get thyroid and lymph node
Why use Saponin when you can get a commercially prepared solution such as
Lysing 1000, which was specifically designed to remove rbc's from Cytology
specimens. Lysing 1000 not only lyses the rbc's but gives you exceptionally
preserved cellular material which is amiable with IHC staining.
American Matertech
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-2907
Original Message
Subject: [Histonet] A Good Human Brain Control
From: Candice Smoots
Thank you to everyone who provided input on preferences for HE stainers last
week. You were all very helpful!
Kendall A. Neely
Histology Technical Specialist
Shands Rocky Point Laboratories
(352) 265-0111, x72113
___
Histonet mailing list
Hi Histonetters!
I hope everyone is having a great day. I just got a new position that
I want to tell you about . The position is Clinical Lab Director. The
position is with a hospital system and you would have the lab managers
from the 5 affiliated labs reporting to you. The position is in
I was curious about any tricks out there for avoiding spills when setting
up the stainer. We will be receiving a new stainer soon which will be taller
and larger than our current one. I'm just worried I will spill chemical
into the surrounding dishes. Would using wash bottles work or are there
Hi all!
I'm looking for recommendations for a xylene substitute for our processing and
staining. We have two VIP's and a Leica stainer. We use Permount for
coverslipping (manually with glass). Does anyone use a xylene substitute
that you would recommend for this combination?
Thank you!
Sheila,
You might want to talk to the Leica rep. My guy was here a couple of weeks
ago and they have a xylene sub and a mouting media that plays nicely with
it. I don't recall the name of the product, but it might be worth talking
to him about it.
Good Luck!
Michelle
-Original
Why did they quit making them and what are others using as a replacement?
Bruce W. Brodersen, DVM, PhD
University of Nebraska Veterinary Diagnostic Center
1900 N. 42nd Street
Lincoln, NE 68583-0907
voice (402) 472-1434
FAX (402 472-3094
___
Histonet
We use Clear-Rite 3 (Richard Allan Scientific 6901) from Fisher Scientific in
our VIP processor and for staining. I am not familiar with Permount, but we
use Richard-Allan Mounting Medium (4111; also available from Fisher Scientific)
that is toluene based - works great in combination with
The following has been found useful in my hands:
Removal of Excess Blood
Haemolysing haemorrhagic specimens cause fewer problems in identifying
individual cells. The removal of red blood cells can be achieved using
Ficoll-Hypaque gradient separation or using a lysis solution such as
isotonic
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