[Histonet] IHC Lead Tech Position - Dallas

2013-12-16 Thread Pat Patterson
LEAD IMMUNOHISTOCHEMISTRY TECHNICIAN

ProPath, a progressive, CAP accredited, high-volume pathology practice in 
Dallas, Texas is seeking an Lead Immunohistochemistry Technician for its' 
Immunohistochemistry Lab.  Responsibilities include slide preparation (paraffin 
and frozen sections), IHC staining using our unique manual system, antibody 
titer preparation, equipment maintenance, supply/reagent inventory maintenance, 
and QC/QA recording.

The ideal candidate will have a minimum of 5 years Histology experience with 
paraffin microtomy with a variety of different tissue types, prefer at least 3 
years immunohistochemistry, immunofluorescence or in situ hybridization and 
frozen section experience.  Technical Lead/Coordinator experience is required.  
Working knowledge of IHC theory required, hands on IHC performance desired.  If 
using an automated system we'll easily train you on our manual system.  HT 
(ASCP) or QIHC desired.

The hours for the position are 7:00 p.m. to 3:30 a.m. Monday through Friday.

ProPath utilizes leading technology and is a quality oriented pathology 
laboratory.  Benefits include medical, dental, Short and Long Term Disability 
insurance, a matched 401K plan and more!

Don't Follow the Leader!  Join the Leader!

To apply, please visit www.propath.com

EOE

Accessibility Accommodations
If you require an accommodation to navigate or apply to our careers site, 
please send your request to accessibil...@propath.com.




Pat Patterson, HTL(ASCP)
Supervisor, Immunohistochemistry
ProPath - The Leader in Pathology Services
1355 River Bend Drive
Dallas, TX 75247

pat.patter...@propath.commailto:pat.patter...@propath.com
214-237-1700 x 2027
214-237-1730 fax

To learn more about ProPath, please visit http://www.ProPath.com



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[Histonet] Charges for recuts on legal cases

2013-12-16 Thread Vickroy, Jim

Can anyone share with me what they charge for doing recuts on cases that have 
been pulled for legal purposes?   I am trying to see what others charge before 
we assign a charge.
I think most people are probably charging by the slide but please let me know 
if you charge differently.

Thanks

James Vickroy BS, HT(ASCP)

Surgical  and Autopsy Pathology Technical Supervisor
Memorial Medical Center
217-788-4046



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RE: [Histonet] Re: Staining on Alcohol Fixed Smears

2013-12-16 Thread Tom McNemar
Since there is no exposure to formalin, we do not do antigen retrieval on 
alcohol fixed specimens.  We use the Ventana Benchmark XT and copy the protocol 
to a new number and use the Wet option rather than paraffin.  No retrieval 
needed.

Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740) 348-4163
(740) 348-4166
tmcne...@lmhealth.org
www.LMHealth.org

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Beth Cox
Sent: Saturday, December 14, 2013 6:30 PM
To: histonet@lists.utsouthwestern.edu; levi.fr...@gmail.com
Subject: [Histonet] Re: Staining on Alcohol Fixed Smears

Levi,

I've worked up most of the more common antibodies on alcohol fixed
smears.  There are two things to remember here:  1) your specimens are
alcohol fixed, meaning antigen retrieval needs are different, and 2)
they are smears, meaning the cells weren't 'cut open' during microtomy,
which impeeds some nuclear staining.  Those are two different issues to
consider.

Some rules of thumb:
1)  most cell membrane antigens will stain nicely with minimal changes
to the protocols you use for FFPE specimens
2)  most cytokeratin antigens stain nicely with little change to your
FFPE protocols (if you need to change, start by cutting your antigen
retrieval time in half)
3)  most nuclear antigens require significant changes from FFPE
protocols, and some are essentially impossible to stain using standard
antibodies.

When I return to work on Monday, I will forward you my protocol
'adjustments' for the antibodies you requested.

Beth Cox, HTL/SCT(ASCP)QIHC
Vagabond Histotech




On 12/14/2013 12:00 PM, histonet-requ...@lists.utsouthwestern.edu wrote:
 Message: 4
 Date: Sat, 14 Dec 2013 18:25:08 +0200
 From: Levi Friedlevi.fr...@gmail.com
 Subject: [Histonet] Staining on Alcohol Fixed Smears.
 To:histonet@lists.utsouthwestern.edu
 Message-ID:
   CA+puqxTXL85pEwvR=sqPQA36tMJPm=sx2kv3gyebrbu0he3...@mail.gmail.com
 Content-Type: text/plain; charset=ISO-8859-1

 Hi Everyone.

 I am looking to stain alcohol fixed smears with a group of antibodies.

 The antibodies of particular interest are p63, p53 and ki67.
 Along with these antibodies I am looking for positive nuclear and
 cytoplastic staining antibodies.

 If anyone has any experience in staining alcohol fixed slides your
 information is very appreciated.

 All the best.

 -- Sincerely, - Levi Fried

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[Histonet] RE: Charges for recuts on legal cases

2013-12-16 Thread Wanda.Smith
I charge a $30.00 fee for investigating the case and issuing a report.  I offer 
1 HE and 2 unstained sections on plus slides and charge an additional $15.00 
per slide.  They furnish the shipping/FedEx.
W

WANDA G. SMITH, HTL(ASCP)HT 
Pathology Supervisor 
TRIDENT MEDICAL CENTER 
9330 Medical Plaza Drive 
Charleston, SCĀ  29406 
843-847-4586 
843-847-4296 fax 

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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Vickroy, Jim
Sent: Monday, December 16, 2013 11:17 AM
To: histonet@lists.utsouthwestern.edu
Cc: Bantner, Diane
Subject: [Histonet] Charges for recuts on legal cases


Can anyone share with me what they charge for doing recuts on cases that have 
been pulled for legal purposes?   I am trying to see what others charge before 
we assign a charge.
I think most people are probably charging by the slide but please let me know 
if you charge differently.

Thanks

James Vickroy BS, HT(ASCP)

Surgical  and Autopsy Pathology Technical Supervisor Memorial Medical Center
217-788-4046



This message (including any attachments) contains confidential information 
intended for a specific individual and purpose, and is protected by law. If you 
are not the intended recipient, you should delete this message. Any disclosure, 
copying, or distribution of this message, or the taking of any action based on 
it, is strictly prohibited.
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[Histonet] Re: Staining on Alcohol Fixed Smears

2013-12-16 Thread Beth Cox
I agree that with no formalin exposure, there is no crosslinking that 
needs to be broken, but a then, do nothing approach to antigen 
retrieval oversimplifies the issue.   Alcohol fixation makes changes in 
the protiens/antibodies also, although different changes than formalin 
does, and these changes need to be accounted for.  In my research on 
alcohol fixed smears, I found that most antibodies perform best with 
some antigen retrieval, often gentler than formalin tissues require.


Beth Cox, HTL/SCT(ASCP)QIHC
Vagabond Histotech

--

Message: 4
Date: Mon, 16 Dec 2013 11:13:59 -0500
From: Tom McNemartmcne...@lmhealth.org
Subject: RE: [Histonet] Re: Staining on Alcohol Fixed Smears
To: 'Beth Cox'bethc...@gmail.com,
histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu,levi.fr...@gmail.com
levi.fr...@gmail.com
Message-ID:
E9A90E28259D2F4E84308C5E8EA8F7B4016951E94252@lmhs-exchange
Content-Type: text/plain; charset=us-ascii


Since there is no exposure to formalin, we do not do antigen retrieval on alcohol fixed 
specimens.  We use the Ventana Benchmark XT and copy the protocol to a new number and use 
the Wet option rather than paraffin.  No retrieval needed.

Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740) 348-4163
(740) 348-4166
tmcne...@lmhealth.org
www.LMHealth.org

-Original Message-
From:histonet-boun...@lists.utsouthwestern.edu  
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Beth Cox
Sent: Saturday, December 14, 2013 6:30 PM
To:histonet@lists.utsouthwestern.edu;levi.fr...@gmail.com
Subject: [Histonet] Re: Staining on Alcohol Fixed Smears

Levi,

I've worked up most of the more common antibodies on alcohol fixed
smears.  There are two things to remember here:  1) your specimens are
alcohol fixed, meaning antigen retrieval needs are different, and 2)
they are smears, meaning the cells weren't 'cut open' during microtomy,
which impeeds some nuclear staining.  Those are two different issues to
consider.

Some rules of thumb:
1)  most cell membrane antigens will stain nicely with minimal changes
to the protocols you use for FFPE specimens
2)  most cytokeratin antigens stain nicely with little change to your
FFPE protocols (if you need to change, start by cutting your antigen
retrieval time in half)
3)  most nuclear antigens require significant changes from FFPE
protocols, and some are essentially impossible to stain using standard
antibodies.

When I return to work on Monday, I will forward you my protocol
'adjustments' for the antibodies you requested.

Beth Cox, HTL/SCT(ASCP)QIHC
Vagabond Histotech




On 12/14/2013 12:00 PM,histonet-requ...@lists.utsouthwestern.edu  wrote:


Message: 4
Date: Sat, 14 Dec 2013 18:25:08 +0200
From: Levi Friedlevi.fr...@gmail.com
Subject: [Histonet] Staining on Alcohol Fixed Smears.
To:histonet@lists.utsouthwestern.edu
Message-ID:
   CA+puqxTXL85pEwvR=sqPQA36tMJPm=sx2kv3gyebrbu0he3...@mail.gmail.com
Content-Type: text/plain; charset=ISO-8859-1

Hi Everyone.

I am looking to stain alcohol fixed smears with a group of antibodies.

The antibodies of particular interest are p63, p53 and ki67.
Along with these antibodies I am looking for positive nuclear and
cytoplastic staining antibodies.

If anyone has any experience in staining alcohol fixed slides your
information is very appreciated.

All the best.

-- Sincerely, - Levi Fried


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[Histonet] RE: Histonet Digest, Vol 121, Issue 21

2013-12-16 Thread Scott A. Ely
re:  per slide cost for IHC

I realize there are differences in reagents, including antibody prices.  Still, 
I sometimes am asked to provide the average cost to produce a single IHC slide.

If anyone has an available estimate, especially broken down (glass cost, 
antibody cost, labor cost...), I would greatly appreciate it.

Thank you.
---
Scott Ely, MD MPH
Associate Director, Hematopathology Fellowship Program
Section of Hematopathology
Department of Pathology
Weill Medical College of Cornell University
New York Presbyterian Hospital
Room:  Starr 715
525 E. 68th Street
New York, NY 10065
PH:  212-746-2442
FAX: 212-746-2009
http://www.cornellphysicians.com/scottely/

Legal Confidentiality Notice: This e-mail message, including any attachments, 
is for the sole use of the original intended recipient(s) selected by Dr. Ely 
and may contain confidential and privileged information.  Any unauthorized 
review, use, disclosure or distribution is prohibited. If you are not the 
recipient specified by  Dr. Ely, please contact the sender by reply e-mail and 
destroy all copies of the original message.
---


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of 
histonet-requ...@lists.utsouthwestern.edu 
[histonet-requ...@lists.utsouthwestern.edu]
Sent: Monday, December 16, 2013 1:07 PM
To: histonet@lists.utsouthwestern.edu
Subject: Histonet Digest, Vol 121, Issue 21

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Today's Topics:

   1. rabbit cea antibody for mouse (Mehmet Fatih BOZKURT)
   2. IHC Lead Tech Position - Dallas (Pat Patterson)
   3. Freezer for tissue storage (Wester, Martha)
   4. RE: Re: Staining on Alcohol Fixed Smears (Tom McNemar)
   5. Charges for recuts on legal cases (Vickroy, Jim)


--

Message: 1
Date: Mon, 16 Dec 2013 09:02:54 +0200
From: Mehmet Fatih BOZKURT fbozk...@gmail.com
Subject: [Histonet] rabbit cea antibody for mouse
To: ih...@googlegroups.com, Histonet@lists.utsouthwestern.edu
Message-ID:
CA+pSMGTJu1mUUKnNydd45UD76AsXv=_oa_t2nma+f-2jlq4...@mail.gmail.com
Content-Type: text/plain; charset=ISO-8859-1

Hello,

I'm looking for rabbit CEA antibody for using on mouse tissue. Anyone can
help me?
Thanks.

--
Mehmet Fatih BOZKURT, DVM, PhD
Afyon Kocatepe University
Faculty of Veterinary Medicine
Department of Pathology
03030, ANS Campus
Afyonkarahisar-TURKEY
Tel: +902722281312-16173/16237


--

Message: 2
Date: Mon, 16 Dec 2013 14:41:51 +
From: Pat Patterson pat.patter...@propath.com
Subject: [Histonet] IHC Lead Tech Position - Dallas
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:
6dcb8b92d0138244b56ce8eace0d458d1675b...@mail.propathlab.com
Content-Type: text/plain; charset=us-ascii

LEAD IMMUNOHISTOCHEMISTRY TECHNICIAN

ProPath, a progressive, CAP accredited, high-volume pathology practice in 
Dallas, Texas is seeking an Lead Immunohistochemistry Technician for its' 
Immunohistochemistry Lab.  Responsibilities include slide preparation (paraffin 
and frozen sections), IHC staining using our unique manual system, antibody 
titer preparation, equipment maintenance, supply/reagent inventory maintenance, 
and QC/QA recording.

The ideal candidate will have a minimum of 5 years Histology experience with 
paraffin microtomy with a variety of different tissue types, prefer at least 3 
years immunohistochemistry, immunofluorescence or in situ hybridization and 
frozen section experience.  Technical Lead/Coordinator experience is required.  
Working knowledge of IHC theory required, hands on IHC performance desired.  If 
using an automated system we'll easily train you on our manual system.  HT 
(ASCP) or QIHC desired.

The hours for the position are 7:00 p.m. to 3:30 a.m. Monday through Friday.

ProPath utilizes leading technology and is a quality oriented pathology 
laboratory.  Benefits include medical, dental, Short and Long Term Disability 
insurance, a matched 401K plan and more!

Don't Follow the Leader!  Join the Leader!

To apply, please visit www.propath.com

EOE

Accessibility Accommodations
If you require an accommodation to navigate or apply to our careers site, 
please send your request to 

[Histonet] Perfusion of mouse bone femur

2013-12-16 Thread Reuel Cornelia
Does anybody have a Protocol for perfusion of mouse bone femur. It looks like 
my protocol does not work.
1.fix in 4% PFA in PBS for 24 hrs in refrigerator
2. wash in PBS 3x 
3. transfer in 14 %EDTA for 5 days.
4. Wash in water for maximum of 2 hrs in running water
6. perfusion with 15% sucrose overnight
7.perfusion with 30% overnight.
8. Transfer in OCT.
8. Cut in 10 um and transfer section on APES slide
 
Results: When cutting section, the tissue does not adhere to the slides 
properly.
 
Can you please help us or any comment to correct this protocol.
 
 
Reuel Cornelia, BS MT, AMT
Cellular Pathology
Texas Scottish Rite Hospital for Children
 Welborn Street
Dallas, TX 75219
Tel: 214-559-7766
fax: 214-559-7768
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[Histonet] RE: Charges for recuts on legal cases

2013-12-16 Thread Cartun, Richard
Here in Connecticut we are not allowed to charge for the preparation of 
pathology slides for legal purposes.

Richard

Richard W. Cartun, MS, PhD
Director, Histology  Immunopathology
Director, Biospecimen Collection Programs
Assistant Director, Anatomic Pathology
Hartford Hospital
80 Seymour Street
Hartford, CT  06102
(860) 545-1596 Office
(860) 545-2204 Fax
richard.car...@hhchealth.org


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Vickroy, Jim 
[vickroy@mhsil.com]
Sent: Monday, December 16, 2013 11:16 AM
To: histonet@lists.utsouthwestern.edu
Cc: Bantner, Diane
Subject: [Histonet] Charges for recuts on legal cases

Can anyone share with me what they charge for doing recuts on cases that have 
been pulled for legal purposes?   I am trying to see what others charge before 
we assign a charge.
I think most people are probably charging by the slide but please let me know 
if you charge differently.

Thanks

James Vickroy BS, HT(ASCP)

Surgical  and Autopsy Pathology Technical Supervisor
Memorial Medical Center
217-788-4046



This message (including any attachments) contains confidential information 
intended for a specific individual and purpose, and is protected by law. If you 
are not the intended recipient, you should delete this message. Any disclosure, 
copying, or distribution of this message, or the taking of any action based on 
it, is strictly prohibited.
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[Histonet] variable staining of alcian blue

2013-12-16 Thread Rui TAHARA
Hello, 

I am staining paraffin sections (10 microns) with Alcian blue and Nuclear Fast 
Red as standard protocol as below. 
The problem is that I see some sections stained with alicain blue show some 
variability (hope i am able to attach image); 
alcian blue stain are washed out in some sections even in the same slide. Those 
sections show pink color in the cartilage. 


Clearing
dehydrate
1% Alcain blue (PH2.5) 30 mins
dip in tap water
running water 2mins
dip deionized water
0.1% Nuclear Fast red 5 mins
dip deionized water 30 sec X 2 
95% ethanol 1min
100% ethanol 1 mins X 2
clearing 

Is this something to do with filtering alcian blue or nuclear fast red? 
I filtered alcian blue using needles to eliminate a big undisolved particle, 
but I did not filter the nuclear fast red since it seems all dissolved well.
also I rarely had the problem last time i used the same staining. 
I know i need to filter with filter paper but when i tried, even with non-fine 
filter paper, it absorbed too much dye and was not successful.  


I tried to wash nuclear fast red with running tap water 1 min and dip in 
deionized water intead of twice wash of deionized water as described above. 
However, variable staining of alcian blue still present. 

Does anybody have same problem before? 
I appreciate any suggestion to solve this. 

Thanks. 

Rui 
 



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