Where can I find the study material needed to prepare for the IHC exam? When
on the ASCP website but found nothing.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Carrie:
The cytospin will not need dewaxing, as you point out, but I do not foresee any
problem when compared with the control. You have to realize that dewaxing the
control is intended only to expose the tissue section to the reagents.
As to the peanut oil if you are trying to stain for common
We are thinking about purchasing a new tissue processor. We have looked
extensively into microwave tissue processors instead of the conventional tissue
processors we are all used to.
Recently two of my techs came back from a symposium and brought me literature
on the Leica Peloris. The
Are there any issues with microwave processing and IHC?
Thanks,
Carol
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Vickroy,
Jim
Sent: Tuesday, May 19, 2009 9:25 AM
To:
Hi Histonetters!
I hope everyone is having a great day. I wanted to do a quick post to tell
you about some of the positions I am working on. All of my positions are
full time permanent positions and my clients offer excellent compensation,
benefits and relocation assistance.
Here are the jobs I
We are using the Peloris and love it! I process small bx type specimens
in 1 hour throughout the day. I process 80% of the rest of our specimens
in 4 hours and the large fatty specimens run for 9 hours. What I also
like is that I do not have to deal with any of the microwave safety regs
and
**
*Hello Histonetters,*
**
*I have an opening for a Lead/Supervisory Histotechnologist in Long Island,
NY. *
**
*Please review the job description and send an updated resume with any other
questions to aly...@alliedsearchpartners.com *
*If you are not interested but you know someone who is, we
No issues using the Milestone products.
Donna
Sent via BlackBerry by ATT
-Original Message-
From: Carol Bryant cb...@lexclin.com
Date: Tue, 19 May 2009 09:35:54
To: Vickroy, Jimvickroy@mhsil.com; Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Leica Peloris versus
Hello Netters,
We are trying to do do immunofluorescence on FFPE tissue sections; we always
get autofluorescence. We have tried Sodium Borohydride treatment, does not work
very well. Does anyone have good method to remove this autofluorescence from
FFPE tissue sections.
We have never tried
We use the Sakura Xpress with no problems.
Jeanine Bartlett
Infectious Diseases Pathology Branch
(404) 639-3590
jeanine.bartl...@cdc.hhs.gov
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Donna
Hello Netters,
I was wondering if anyone has a reference or knows where I can track
down information on determining the end point of potassium permanganate
filters by dropping the used portion of the filter particulate into
water.
I have heard that if you drop the used filter particulate
Blount Memorial Hospital in Maryville, TN has a histology technician
position open Monday thru Friday 7-3:30.
We are located just minutes from the beautiful Smoky Mountains National
Park and experience 4 wonderful seasons! All types of outdoor activities
are possible. Maryville is host to the
You wrote: We are trying to do do immunofluorescence on FFPE tissue
sections; we always get autofluorescence. We have tried Sodium Borohydride
treatment, does not work very well. Does anyone have good method to remove
this autofluorescence from FFPE tissue sections.
We have never tried Toluidine
Does anyone in histoland use this coverslipper? What do you like about it?
What do you not like about it?
Best regards,
Patsy
Patsy Ruegg, HT(ASCP)QIHC
IHCtech, LLC
Fitzsimmons BioScience Park
12635 Montview Blvd. Suite 215
Aurora, CO 80010
P-720-859-4060
F-720-859-4110
wk email
We do sequential immunostaining to avoid cross reaction of a secondary
antibody to the next primary antibody, and also perform a normal serum block
that binds to the first secondary antibody:
Two examples using two rat antimouse primaries and with immunofluorescent
method. This is done on
Has anyone successfully used Santa Cruz's MetAP-2 for IHC in FFPE mouse
and rat sections? I am starting for scratch and am trying to find info
on dilution range and antigen retrieval methods. The spec sheet only
lists recommendations for applications other than IHC.
Any info is greatly
Does anyone have a .pdf copy of the instructions manual for the Nikon Diaphot
300 Inverted Microscope they could send me?
Thanks,
Michael Norman
The information contained in this email may be confidential and/or legally
privileged. It has been sent for the sole
How do I go about finding the study material needed for the IHC exam,
how do I prepare, etc.
Thanks
Ginny Achstetter
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
Last week, my former employer, Loyola University Medical Center in Maywood,
Il., layed off 440 employees (about 8 % of the workforce).
I was the Manager of Anatomic Pathology
(Histo/Cyto/Autopsy/Transcription/MohsLabs/Clerical Support) and now am looking
for a career opportunity in the
I am looking for a career opportunity.
- Forwarded Message -
From: jimr0...@comcast.net
To: Histonet2 histonet@lists.utsouthwestern.edu
Sent: Tuesday, May 19, 2009 12:14:08 PM GMT -06:00 US/Canada Central
Subject: Career Opportunity in Chicago area
Last week, my former
just testing to see if I can post
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Hello Histoneters,
I was wondering if someone could contact me offline about CLIA regulations
and/or inspections. I have a few concerns. Any help would be appreciated.
Thanks in advance.
JD
jdhi...@yahoo.com
___
Histonet mailing list
I'm hoping to network with some wonderful Pathologists (and informaticists).
I'm wondering if anyone out there has ever used or been a part of an
implementation of Cerner Millennium's PathNet HLA module for tissue transplant.
Any networking and advice is greatly appreciated!!
Lori M. Brown,
Hi Rene,
Thanks for the info. We are doing a AFB Fites for Nocardia. There is
filamentous bacteria in the patient GMS and the docs are differentiating the
type. I did not deparaffinize the patient cytospin slides and I did
deparaffinize the patient control with Z/PO. The problem I had been
Hi Tony,
Thanks for the info. I understand the discussion topic. I just wish their was
one straight answer! But then this is histology!
Carrie
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
I was able to speak to Larry M. about my tissue processor problems. thank
you all for your help.
I am now looking for perhaps a broken MVP-1 or 2 since I am no longer able to
get the CRT display parts to fix mine. they are interchangeable and if I
could find a discarded MVP I
Does anyone have any suggestions or protocols for cryoprotecting unfixed
mouse heart tissue? Some of the ones I have been cryosectioning lately have
been damaged, I think because of improper cryoprotection.
Thanks!
Adam
baza0...@umn.edu
___
Adam,
It is not a good to sucrose cryoprotect fresh tissues. Only well fixed
tissues should be cryoprotected to lessen freezing artifact caused by large
water ice crystals. Charles Scouten, on his website discusses this, and if
one cryoprotects fresh tissues, you change the osmolarity within
For all information about certification exams (e.g., HT, HTL, SLS
(specialist in laboratory safety), or on qualification exams (e.g., QIHC),
go to
www.ascp.org
Click on Laboratory Professional
Click on Certification
Click on either Get Certified or Get Qualified
Under Get Qualified, there is
29 matches
Mail list logo