I have done this in the research world, but I don't have any experience
with clinical analysis of this protein.
I will tell you that cell signalling have the best antibodies in this
space, IMHO:
https://www.cellsignal.com/browse/?Ntk=Products&N=4294956287&Ntt=atm+
A company that you can actually
Anyone doing IHC testing for "Ataxia-telangiectasia-mutated protein" expression
on FFPE tissue? Thank you.
Richard
Richard W. Cartun, MS, PhD
Director, Histology & The Martin M. Berman, MD Immunopathology & Morphologic
Proteomics Laboratory
Director, Biospecimen Collection Programs
Assistant D
Hi Histonetters! We are looking for a full time licensed HISTOTECHNOLOGIST here
in our very busy Delray Florida Dermatology Lab. This is a permanent full time
NIGHT SHIFT (40 hours) position with benefits (medical/401k/vacation) and shift
differential. THIS IS A DRUG FREE WORKPLACE. Background c
We use freezer boxes and then record what is in the freezer boxes on a
worksheet that is kept in an excel file. The excel file has all of the boxes
in it.
Here is an example of one of the pages
BOX 6 - Full
name
vendor
catalog #
lot #
date alqt
ul/aliquot
notes
AGE
Biorbyt
Ronnie
We have these protocols in place for porcine tissue. We use the roche kit for
tunel 11684809910 and for CC3 we use the cell signaling antibody 9664.
Liz
Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Premier Laboratory, LLC
PO Box 18592
Boulder, CO 80308
(303) 682-3949 office
(303) 682-9060
Is anyone working on this just now? And more specifically on the pig species?
Any pointers would be appreciated
Thanks
Ronnie Houston, MS HT(ASCP)QIHC FIBMS
Anatomic Pathology Manager
Laboratory Services
700 Children's Drive
Columbus, OH 43205
(P) 614-722-5450
(F) 614-722-2899
ronald.hous...@nati
Apply gently heated water on the sections in a way that the gelatin is washed
out.René
On Tuesday, August 16, 2016 4:48 AM, Monica Aguilera via Histonet
wrote:
Dears,
I was wondering if some of you might have experience in the following:
We have had a lot of problems cutting WAT tiss
I used to have several compartmented plastic alphabetized boxes with enough
empty spaces to accommodate "new arrivals". If the spaces were used-up I just
added a new box. Since they occupied several shelves, each shelf had the
lettering identifying the boxes in each one.René
On Tuesday, Au
Usually you do not pour 10%NBF onto a specimen; you place the specimen onto a
container/vial with the 10%NBF.René
On Tuesday, August 16, 2016 9:29 AM, Mike Pence via Histonet
wrote:
I know this might sound a bit crazy, but does anyone have a written policy and
procedure for dispensing
I know this might sound a bit crazy, but does anyone have a written policy and
procedure for dispensing 10% formalin onto a surgical specimen? If you do,
would you be willing to share?
Michael S. Pence | Supervisor of Laboratory Services
Great River Health Systems
1221 S. Gear Ave. | West Burlin
Hi all,
In our lab we carry out quite a number of IHCs for research purposes.
The number of mAbs and pAb stored in the frezeer is getting to the point
that, when you need to do and IHC, you actually lose more time diving
through the frezeer draws for the right vial than doing the IHC! is not
Dears,
I was wondering if some of you might have experience in the following:
We have had a lot of problems cutting WAT tissue either directly embedded
in OCT or pre-fixed with PFA or formalin (either cold or and them embedded
with OCT.
We solved this problem following Ryan Berry et al, 2014 pape
12 matches
Mail list logo