Dear all
Is anyone practising microtome calibration for thickness of sections cut?
Our GLP auditors are frequently asking for it.
They also suggest that automatic tissue processor time in each reagent
should be calibrated.
any comments
Regards
Dr Girish
India
Disclaimer
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Happy Halloween!
Does anyone know of a good PIN-4 control? We are currently using
in-house tissue but are finding a lot of variance with the stainability.
If anyone knows of a good source I would greatly appreciate it.
Thanks in advance,
Sharon Campbell, HTL(ASCP)CM, BSBM
Histology
Are they the same ?
Kimberly C. Tuttle HT (ASCP)
Pathology Biorepository and Research Core
University of Maryland
Room NBW58, UMMC
22 S. Greene St
Baltimore, MD 21201
(410) 328-5524
(410) 328-5508 fax
This e-mail and any accompanying attachments may be privileged, confidential,
contain
Hi,
Any recommedations for anti-mouse ferritin antibodies (looking to stain FFPE
mouse tissue).
Thanks,
Kim
Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA
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Dear Dr. Girish,
I agree with rene, if the qualitiy of the cuts is fine it doesn't matter if they
are 1µm or 2.3µm thick.
But I'm highly interested in how your GLP auditors want to calibrate the
thickness of the section cuts. Are you supposed to measure the slides after
cutting?! Before or after
Frauke:
That calibration is ussually done by measuring the advance mechanism of the
block holder and how many µm the block moves towards the blade, but that is
rubbish.
René J.
--- On Fri, 10/31/08, Dr. med. Frauke Neff [EMAIL PROTECTED] wrote:
From: Dr. med. Frauke Neff [EMAIL PROTECTED]
We have a GLP person who is not familiar with Histology at all. We have had
to educate her about these issues and may other things. Calibration finally
came down to having a PM on the units every year. After she understood all
the things we do with a section during the cutting phase and pick up
I have been (unsuccessfully) trying to find a polyclonal antibody
against human proteolipid protein (stains myelin) that will work with
immunofluorescence on FFPE sections. I have also tried some myelin basic
protein with no luck. Has anyone found any in the past that have
worked??
Thanks!
Happy Halloween... I'm looking for a source of monitoring badges for formalin
and xylene, both the 8 hour TWA and the STEL.
Thank you, Sandy
Sandra Cheasty
Histology Supervisor
UW-Madison
School of Veterinary Medicine
608 263-1680
ASSAY TECHNOLOGY
1252 Quarry Lane
Pleasanton, CA 94566
1-800-833-1258
Sandra Cheasty [EMAIL PROTECTED] 10/31/2008 08:51
Happy Halloween... I'm looking for a source of monitoring badges for formalin
and xylene, both the 8 hour TWA and the STEL.
Thank you, Sandy
Sandra Cheasty
Histology
Try Mercedes Medical.
http://www.mercedesmedical.com/
Linda Blazek HT (ASCP)
Manager/Supervisor
GI Pathology of Dayton
7415 Brandt Pike
Huber Heights, OH 45424
Phone: (937) 293-4424 ext 7118
Email: [EMAIL PROTECTED]
-Original Message-
From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED]
Morphix Technologies
www.morphtec.com
757-431-2260
-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Kathleen
Boozer
Sent: Friday, October 31, 2008 11:22 AM
To: histonet@lists.utsouthwestern.edu; Sandra Cheasty
Subject: Re: [Histonet] Formalin and Xylene
Cindi Robinson replied to me offline, saying some of the things Vinnie
della Speranza also said. I wasn't aware that hydrochloric acid
decalcification (I assume that regular brand-name Decal is HCl) with
prompt timing degraded IHC - something I guess that every lab has to
determine for themselves.
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