Any input as to preferred instruments would be greatly appreciated...
Leigh
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Biocare Decloaker here !!
Brett M. Connolly, Ph.D.
Principal Scientist, Imaging Dept.
Merck Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
brett_conno...@merck.com
T- 215-652-2501
F- 215-993-6803
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
I second that!
Linda Blazek HT (ASCP)
Manager/Supervisor
GI Pathology of Dayton
Digestive Specialists, Inc
Phone: (937) 396-2623
Email: lbla...@digestivespecialists.com
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
Third that.
Jan S
On Tue, Apr 30, 2013 at 8:58 AM, Blazek, Linda
lbla...@digestivespecialists.com wrote:
I second that!
Linda Blazek HT (ASCP)
Manager/Supervisor
GI Pathology of Dayton
Digestive Specialists, Inc
Phone: (937) 396-2623
Email: lbla...@digestivespecialists.com
Jackie...
We have ordered these from a company by the name of Centurian Medical. The lids
are sold separately.
Valerie
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jackie O'Connor
Sent: Wednesday,
dingers...@aplaboratories.com
Original Message
Subject: RE: [Histonet] HIER = pressure cookers
From: Blazek, Linda [1]lbla...@digestivespecialists.com
=
Date: Tue, April 30, 2013 9:58 am
To: Connolly, Brett M
Too much blue is mostly a problem of too less red.
Have you checked your Eosin? pH? Rinsing after eosin?
My personal issue was sometimes too thin sections. Those looked also rather
pale.
Gudrun
-Ursprüngliche Nachricht-
Von: histonet-boun...@lists.utsouthwestern.edu
I attended the Tri-State Symposium in Dubuque, IA last week (which was
fantastic) and sat in on a Boot Camp for Histology workshop. At this
workshop I realized that some problems we have been having with sectioning
could be due to our processor set up.
Before microtomy we have to soak our
We use 10 % Neutral Buffered Formalin. It is a wonderful fixative and gives
us really great fixation.
It does sound like you are overly dehydrating your tissues.
Valerie A. Hannen, MLT(ASCP),HTL,SU(FL)
Histology Section Chief
Parrish Medical Center
951 N. Washington Ave.
Titusville, Florida
Hi All,
We are looking to purchase 2 cassette labelers and would like some feedback on
which ones you might recommend. Also, is there a difference between Thermo's
Printmate and Microwriter? Looks like the Printmate is just a newer version.
Your input would be greatly appreciated.
Thanks,
We use a Cuisinart Pressure Cooker that we purchased at Cell Marque. Basically
they buy these pressure cookers and validate them at their facility, I think it
was around $400. Works great!
Katy Eichorn, HT (ASCP) | Histology Supervisor |
Oro Valley Hospital | 1551 E. Tangerine Road | Oro
Hello Histonet,
I have a question for the group at large. How are labs monitoring drift in IHC
staining over time?
Here's the scenario: You do lot to lot testing and everything looks fine until
one day your pathologists are telling you that the CAM5.2 is too dark. Now,
you've been looking
Hi,
I was wondering if anyone still uses the ion-exchange decal method and/or the
electrolytic decal method? If so, could I get some pictures to put in my
power points online?
Also, to any of the new HT or HTL's are there any questions on the registry
exam about those methods? My latest
What title do most use for someone who does gross and is not a PA?
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
histonet-requ...@lists.utsouthwestern.edu
Sent: Tuesday, April 30, 2013 12:02 PM
To:
Ashley,
Every new lot of antibody we get in is run with some of our control tissues and
compared to the current/previous lot staining. So we should be able to detect
a change. Our policy is that minor changes to protocols are OK but anything
major would require revalidation...we try not to
I suggest you look at either a heat transfer or laser etch product. The laser
jet printers can be a bit of a maintenance issue. Also, you need to choose by
the information needed on the cassette. 2D bar coding will take some time to
print and requires precision in the printing. This is an
Grossing Tech
Vanessa
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Barr,Kaye H
Sent: Tuesday, April 30, 2013 12:49 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] RE: Histonet Digest,
dingers...@aplaboratories.com
---= - Original Message
Subject: [Histonet] RE: Histonet Dige= st, Vol 113, Issue 30
From: Barr,Kaye H [1]khb...@mdanderson.org
Date: Tue, April 30, = 2013 1:48 pm
To: '[2]histonet@lists.utsouthwestern.edu'
Michele-
I agree with Mr. DeSalvo. These vendors will be HAPPY to come in an set up a
demo. Some products are better than others, but it needs to fit into your
workflow to be successful. We ended up going with General Data and have been
very happy with their product.
Nancy Schmitt MLT,
In your example you acknowledge that your pathologist is right. In consequence
you go back to your protocol and, more importantly, to the lot that cause your
pathologist's concern and analyze if it contains the same amount of antibody.
By the way, you should have tested the lot to avoid the
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