RE: [Histonet] please remove me

2014-07-14 Thread Weems, Joyce K.
Hi Carolyn,

You must go to this website 
http://lists.utsouthwestern.edu/mailman/listinfo/histonet  and do this yourself.

Best,

Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org



www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
Atlanta, GA 30342

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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Carolyn Thompson
Sent: Saturday, July 12, 2014 5:14 PM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] please remove me

Carol Thompson

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[Histonet] Storage of HER2 neu control slides

2014-07-14 Thread Sebree Linda A
Good morning,

I'd like to get some opinions on the storage of positive control slides for 
HER2 neu.  We currently keep a number of positive control slides in a -20 
degree freezer as some antigens tend to lose reactivity at room temperature; ER 
and PR come to mind.  What has peoples' experiences been with the storage of 
these control slides?

Thanks for any and all replies,

Linda


Linda A. Sebree
University of Wisconsin Hospital  Clinics
IHC/ISH Laboratory
600 Highland Ave.
Madison, WI 53792
(608)265-6596
FAX: (608)262-7174



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[Histonet] FT DERM POSITION DELRAY BEACH, FLORIDA

2014-07-14 Thread Delray Beach Pathology Kari Simeone
Hi Histonetters! We are looking for a full time licensed histotech here in our 
very busy Delray Florida Derm Lab. This is a permanent full time position with 
benefits (medical/401k/vacation).

***PLEASE NO HEAD HUNTERS/PLACEMENT SERVICES***!!!
 Email your resume to lengim...@leavittmgt.commailto:lengim...@leavittmgt.com 
if interested.

*full time position Mon-Fri 11a-7:30p (hours NON NEGOTIABLE)
*MUST be licensed as a FL histotechnologist or technician
*MUST have at least 2 years experience (dermatology preferred)
*VERY proficient in embedding and microtomy
*experience in grossing and immunohistochemistry (BOND) a plus
*must be self motivated and a team player
*knowledge in operating Ventana and Leica equipment desired (not necessary)



Kari M Simeone

ksime...@leavittmgt.commailto:ksime...@leavittmgt.com







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[Histonet] RE: Storage of HER2 neu control slides

2014-07-14 Thread Cartun, Richard
We keep all of our positive control slides at RT.  The breast predictive marker 
slides often sit for a few weeks (after cutting) before being used.  I think 
everyone's situation will be different due to laboratory humidity, tissue 
fixation, and tissue processing which removes the water from the tissue which 
has been shown to be the one of the culprits in antigen degradation in stored 
unstained slides.

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) 972-1596 Office
(860) 545-2204 Fax
richard.car...@hhchealth.org


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sebree Linda A
Sent: Monday, July 14, 2014 8:44 AM
To: Histonet (Histonet@lists.utsouthwestern.edu)
Subject: [Histonet] Storage of HER2 neu control slides

Good morning,

I'd like to get some opinions on the storage of positive control slides for 
HER2 neu.  We currently keep a number of positive control slides in a -20 
degree freezer as some antigens tend to lose reactivity at room temperature; ER 
and PR come to mind.  What has peoples' experiences been with the storage of 
these control slides?

Thanks for any and all replies,

Linda


Linda A. Sebree
University of Wisconsin Hospital  Clinics IHC/ISH Laboratory
600 Highland Ave.
Madison, WI 53792
(608)265-6596
FAX: (608)262-7174



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RE: [Histonet] RE: Storage of HER2 neu control slides

2014-07-14 Thread Joelle Weaver
I do the complete drain  dry, date, then refrigeration. Use them within 6 
weeks. The Oracle IVD, IFU says bake overnight, but I don't see that happening 
too often. 


Joelle Weaver MAOM, HTL (ASCP) QIHC


  

 
 From: richard.car...@hhchealth.org
 To: lseb...@uwhealth.org; Histonet@lists.utsouthwestern.edu
 Date: Mon, 14 Jul 2014 14:22:43 +
 CC: 
 Subject: [Histonet] RE: Storage of HER2 neu control slides
 
 We keep all of our positive control slides at RT.  The breast predictive 
 marker slides often sit for a few weeks (after cutting) before being used.  I 
 think everyone's situation will be different due to laboratory humidity, 
 tissue fixation, and tissue processing which removes the water from the 
 tissue which has been shown to be the one of the culprits in antigen 
 degradation in stored unstained slides.
 
 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) 972-1596 Office
 (860) 545-2204 Fax
 richard.car...@hhchealth.org
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sebree Linda A
 Sent: Monday, July 14, 2014 8:44 AM
 To: Histonet (Histonet@lists.utsouthwestern.edu)
 Subject: [Histonet] Storage of HER2 neu control slides
 
 Good morning,
 
 I'd like to get some opinions on the storage of positive control slides for 
 HER2 neu.  We currently keep a number of positive control slides in a -20 
 degree freezer as some antigens tend to lose reactivity at room temperature; 
 ER and PR come to mind.  What has peoples' experiences been with the storage 
 of these control slides?
 
 Thanks for any and all replies,
 
 Linda
 
 
 Linda A. Sebree
 University of Wisconsin Hospital  Clinics IHC/ISH Laboratory
 600 Highland Ave.
 Madison, WI 53792
 (608)265-6596
 FAX: (608)262-7174
 
 
 
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 contact the sender by reply e-mail and destroy all copies of the original 
 message, including any attachments.
 
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[Histonet] please remove me

2014-07-14 Thread Huimin Wang
please remove me, thanks



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[Histonet] RE: please remove me

2014-07-14 Thread Lavigne, Lisa
Please remove me, thanks

Lisa LaVigne CT, MB(ASCP)
Pathology Manager, St. Peter's Health Partners
315 S. Manning Blvd.
Albany, NY 12208
518-525-5274
lisa.lavi...@sphp.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Huimin Wang
Sent: Monday, July 14, 2014 10:39 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] please remove me

please remove me, thanks



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RE: [Histonet] RE: Storage of HER2 neu control slides

2014-07-14 Thread Sebree Linda A
Thanks Joelle.

I'm surprised that Oracle is suggesting overnight baking as I noticed a huge 
difference when I dried some test tissue controls for 30 @ 60 degrees vs 10 @ 
60 degrees.  I was testing some blocks that I had 3 cores  of varying degrees 
of intensity.  All showed much decreased reactivity at 30 vs 10.  In fact, 
the 2 weaker cores were virtually negative.  I can only assume you're using a 
different clone than we are and that there is different epitope stability 
between clones.

Thanks for your response,

Linda


Linda A. Sebree
University of Wisconsin Hospital  Clinics
IHC/ISH Laboratory
600 Highland Ave.
Madison, WI 53792
(608)265-6596
FAX: (608)262-7174

From: Joelle Weaver [mailto:joellewea...@hotmail.com]
Sent: Monday, July 14, 2014 9:25 AM
To: Cartun, Richard; Sebree Linda A; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: Storage of HER2 neu control slides

I do the complete drain  dry, date, then refrigeration. Use them within 6 
weeks. The Oracle IVD, IFU says bake overnight, but I don't see that happening 
too often.


Joelle Weaver MAOM, HTL (ASCP) QIHC





 From: richard.car...@hhchealth.orgmailto:richard.car...@hhchealth.org
 To: lseb...@uwhealth.orgmailto:lseb...@uwhealth.org; 
 Histonet@lists.utsouthwestern.edumailto:Histonet@lists.utsouthwestern.edu
 Date: Mon, 14 Jul 2014 14:22:43 +
 CC:
 Subject: [Histonet] RE: Storage of HER2 neu control slides

 We keep all of our positive control slides at RT. The breast predictive 
 marker slides often sit for a few weeks (after cutting) before being used. I 
 think everyone's situation will be different due to laboratory humidity, 
 tissue fixation, and tissue processing which removes the water from the 
 tissue which has been shown to be the one of the culprits in antigen 
 degradation in stored unstained slides.

 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) 972-1596 Office
 (860) 545-2204 Fax
 richard.car...@hhchealth.orgmailto:richard.car...@hhchealth.org


 -Original Message-
 From: 
 histonet-boun...@lists.utsouthwestern.edumailto:histonet-boun...@lists.utsouthwestern.edu
  [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sebree Linda 
 A
 Sent: Monday, July 14, 2014 8:44 AM
 To: Histonet 
 (Histonet@lists.utsouthwestern.edumailto:Histonet@lists.utsouthwestern.edu)
 Subject: [Histonet] Storage of HER2 neu control slides

 Good morning,

 I'd like to get some opinions on the storage of positive control slides for 
 HER2 neu. We currently keep a number of positive control slides in a -20 
 degree freezer as some antigens tend to lose reactivity at room temperature; 
 ER and PR come to mind. What has peoples' experiences been with the storage 
 of these control slides?

 Thanks for any and all replies,

 Linda


 Linda A. Sebree
 University of Wisconsin Hospital  Clinics IHC/ISH Laboratory
 600 Highland Ave.
 Madison, WI 53792
 (608)265-6596
 FAX: (608)262-7174



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[Histonet] New Histology Opportunity - Chicago

2014-07-14 Thread Matt Ward
Good morning! 

 

We have had a top company open a new Field Histology Specialist to cover the
Chicago and Midwest Region. The company is a world leading histology
manufacturer and this opportunity is perfect for a histology professional
who is looking to break out of the laboratory and into the field. 


The position offers a competitive salary + bonus, company car, paid
expenses, and full benefits. 


If you or someone you may know would be interested in learning more, please
contact me directly at m...@personifysearch.com. 

 

Thanks!


Matt 

 

Matt Ward

Program Manager 

Personify

5020 Weston Parkway Suite 315

Cary NC 27513 

(Tel) 919.459.3654

(Tel) 800.875.6188 direct ext 103

(Fax) 919.882.8727

  http://www.personifysearch.com/ www.personifysearch.com

 

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[Histonet] IHC Validation

2014-07-14 Thread Leslie Graves
Does anyone have a sample IHC Validation worksheet that they used in their
lab for review.  I know that the requirements have changed since our last
inspection.  I want to make sure that I am including all of the criteria,
and would like to see how other labs are documenting this process.

Leslie Graves
Technical Specialist
Cape Fear Valley Medical Center
1638 Owen Drive
Fayetteville, NC 28341
910-615-6142
lg...@capefearvalley.com
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[Histonet] Bone Marrow Trephine Cases

2014-07-14 Thread Vickroy, Jim

Over the past several years we have had some questions by our 
hematopathologists regarding the quality of the trephine blocks.  The biggest 
concern has been that the sections seem to have  a fragmented appearance which 
we have determined in the past to be areas where the lipid cell borders break.  
 We have found that the artifact is diminished when we pick the sections up as 
quickly as we can which led us to believe that the cell borders break when they 
are left on the   warm water in the waterbath.  Some of the pathologists still 
believe the artifact is caused by the decalcification process.

I have reviewed protocols before and obviously found that labs use different 
decalcifying agents from a harsh HCL solution to a weaker formic acid solution. 
 We currently use Immunocal which I believe is a formic acid solution.   I have 
also been introduced to some new instrumentation available such as the 
Milestone Bone Station which uses a EDTA solution with some added heat and 
agitation.  I realize that EDTA  yields more DNA and RNA which is obviously an 
advantage however the length of time for the decal process with EDTA is much 
longer.   I'm not sure that using EDTA for decalcification will however reduce 
the artifact that the pathologists see (fragmentation and breaking up of the 
lipid cells in the sections.

I would appreciate any information that others might be able to share from 
their experiences and if they have dealt with a similar problem.

Thanks



James Vickroy BS, HT(ASCP)

Surgical  and Autopsy Pathology Technical Supervisor
Memorial Medical Center
217-788-4046
217-415-7505 Cell




  
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[Histonet] IHC for Adrenal hormones?

2014-07-14 Thread Cartun, Richard
Is anyone doing IHC for adrenal corticosteroid and androgen hormones?  We have 
an adrenal tumor in a 10 y.o. patient and the clinicians want to see what the 
tumor is producing.  Thank you.

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) 972-1596 Office
(860) 545-2204 Fax
richard.car...@hhchealth.orgmailto:richard.car...@hhchealth.org


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[Histonet] Used Benchmark

2014-07-14 Thread Travis Troyer
I have a used Ventana Benchmark that is collecting dust in our storeroom.
Would anyone be interested in this piece of equipment?   I have pics and
would be willing to answer any questions. When we put it in the store
room it was in working order.

 

Thanks,

Travis

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