[Histonet] uncertainity of results in histopathology

2011-08-02 Thread tahseen
Dear all please guide me about uncertainity of results in Histopathology
at different steps,including fixation of tissue
,grossing,processing,microtomy,staining,IHC,special staining and
interpretation etc.
This is the requirement of ISO 15189 CLAUSE:5.6.2
Muhammad Tahseen
SKMCHRC
Pakistan


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Re: [Histonet] Mouse vs. Human cells

2011-08-02 Thread Kim Merriam
Years ago, we used to distinguish human fibroblasts in mouse tissue with 
vimentin; which stains human cells quite nicely, but does not cross to mouse.
 
Kim

Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA

From: Carl Postenka cposte...@hotmail.com
To: sdys...@mirnarx.com; histonet@lists.utsouthwestern.edu
Sent: Tuesday, August 2, 2011 11:16 AM
Subject: RE: [Histonet] Mouse vs. Human cells


We've had succes identifying human cells in a mouse background using an 
antibody against human mitochondria (Neomarkers cat#MS-1372P). The primary is a 
monoclonal mouse anti-human, so we use a Dako ARK kit (#K3954) to eliminate the 
mouse on mouse background. HIER using citrate pH=6.0. H2O2 block. Primary 
diluted 1/100 (through ARK kit), for 20min @ R/T.


--
Carl PostenkaLondon Regional Cancer Program


 Date: Mon, 1 Aug 2011 12:55:54 -0500
 From: sdys...@mirnarx.com
 To: Histonet@lists.utsouthwestern.edu
 CC: 
 Subject: [Histonet] Mouse vs. Human cells
 
 Hello Histo-hotties!
 
 Question: We are working with xenograft tumors in mice.  The tumor cells
 are human in origin.  I am trying to come up with some kind of stain
 that will stain all the mouse cells and none of the human cells.  Just
 to be able to determine if any of the human tumor cells are in a normal
 looking say liver.  I was thinking maybe Ki-67?  It doesn't have to be
 any specific marker, just to be able to see a really blue mouse organ,
 and then if there are human cells of any type in the organ light up that
 one cell.
 
 Thanks
 
  
 
  
 
 Sarah Goebel-Dysart, BA, HT(ASCP)
 
 Histotechnologist
 
 Mirna Therapeutics
 
 2150 Woodward Street
 
 Suite 100
 
 Austin, Texas  78744
 
 (512)901-0900 ext. 6912
 
  
 
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[Histonet] Job opening

2011-08-02 Thread Tim Jay
GI path lab in Santa Rosa, CA looking for a certified tech. Great 
opportunity!!! Great pay. Flexible hours. Friendly office. 
Submit resumes to tja...@yahoo.com. 

Sent from my iPhone
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[Histonet] hmm

2011-08-02 Thread sdysart
Has anyone ever heard of the company, Stem cells?  I have been trying to
contact them all morning to order an antibody, but no one ever answers
the phone.  Little nervous.

 

Sarah Goebel-Dysart, BA, HT(ASCP)

Histotechnologist

Mirna Therapeutics

2150 Woodward Street

Suite 100

Austin, Texas  78744

(512)901-0900 ext. 6912

 

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RE: [Histonet] IHC service ??

2011-08-02 Thread Sebree Linda A
We've had excellent service from Ventana and they do have to travel from 
usually Chicago up to Madison.



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Inman, Anna
Sent: Mon 8/1/2011 11:30 AM
To: histonet@lists.utsouthwestern.edu.
Subject: [Histonet] IHC service ?? 




   Can you tell me what kind of on-site technical service you are
accustomed to receiving from Ventana (especially if you NOT in a big
city so travel is required)?  We have had a terrible time getting a
Field service engineer into our lab this year and wonder if that is the
norm for Ventana these days?



For the Dako users - what kind of service are you getting?



Thank you in advance



Anna

anna.in...@stmarygj.org



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[Histonet] cell blocks

2011-08-02 Thread Clare Thornton
How does everyone process their cell blocks?  Currently, we use our biopsy run 
for smaller cell blocks, but the larger ones we use our routine tissue process. 
 Our lab manager would like us to look at putting all cell blocks, regardless 
of size, on our biopsy run, to increase turn around time.  I have my doubts, 
since some cell blocks, especially bronch washes and pleural fluids, can be 
quite large and greasy or mucous-y.  What does everyone else do?  We use 
standard 10% NBF, xylene, and paraplast xtra on our processors.  We would 
process on a Leica Peloris.  Our standard bx protocol is about 1.5 hours total, 
and our standard routine protocol is about 7 hours.

Thank you!

Clare J. Thornton, HTL(ASCP),QIHC
Assistant Histology Supervisor
Dahl-Chase Diagnostic Services
417 State Street, Suite 540
Bangor, ME 04401
cthorn...@dahlchase.com

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[Histonet] SOX-11

2011-08-02 Thread Marian Powers
Hi:  Has anyone had success with antibody SOX-11 and would be willing to
share your protocol?

Thanks in advance,


-- 

*Marian L. Powers*

*Q*uality *L*aboratory *C*onsultants


*Doctors Pathology Services * **
c| 302.747.0580
o| 302.677. ext: 110
f | 302.677.0010
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Re: [Histonet] cell blocks

2011-08-02 Thread Rene J Buesa
I always processed cell blocks, regardless of their size, with the regular 
tissue processing protocol.
René J.

--- On Tue, 8/2/11, Clare Thornton cthorn...@dahlchase.com wrote:


From: Clare Thornton cthorn...@dahlchase.com
Subject: [Histonet] cell blocks
To: 'Histonet@lists.utsouthwestern.edu' Histonet@lists.utsouthwestern.edu
Date: Tuesday, August 2, 2011, 1:14 PM


How does everyone process their cell blocks?  Currently, we use our biopsy run 
for smaller cell blocks, but the larger ones we use our routine tissue 
process.  Our lab manager would like us to look at putting all cell blocks, 
regardless of size, on our biopsy run, to increase turn around time.  I have my 
doubts, since some cell blocks, especially bronch washes and pleural fluids, 
can be quite large and greasy or mucous-y.  What does everyone else do?  We use 
standard 10% NBF, xylene, and paraplast xtra on our processors.  We would 
process on a Leica Peloris.  Our standard bx protocol is about 1.5 hours total, 
and our standard routine protocol is about 7 hours.

Thank you!

Clare J. Thornton, HTL(ASCP),QIHC
Assistant Histology Supervisor
Dahl-Chase Diagnostic Services
417 State Street, Suite 540
Bangor, ME 04401
cthorn...@dahlchase.com

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Re: [Histonet] cell blocks

2011-08-02 Thread Nicole Tatum
you definitly can run them together. I would just test one before I put
them all in there, because when they are small they can over process and
be very hard and brittle making intrepretation difficult. As far as your
larger fatty gooey specimens. Make sure they are no thicker than 3mm.
Anything bigger doesnt process well on a normal 7hr cycle.

Hope this helps
Nicole Tatum HT ASCP









How does everyone process their cell blocks?  Currently, we use our biopsy
 run for smaller cell blocks, but the larger ones we use our routine tissue
 process.  Our lab manager would like us to look at putting all cell
 blocks, regardless of size, on our biopsy run, to increase turn around
 time.  I have my doubts, since some cell blocks, especially bronch washes
 and pleural fluids, can be quite large and greasy or mucous-y.  What does
 everyone else do?  We use standard 10% NBF, xylene, and paraplast xtra on
 our processors.  We would process on a Leica Peloris.  Our standard bx
 protocol is about 1.5 hours total, and our standard routine protocol is
 about 7 hours.

 Thank you!

 Clare J. Thornton, HTL(ASCP),QIHC
 Assistant Histology Supervisor
 Dahl-Chase Diagnostic Services
 417 State Street, Suite 540
 Bangor, ME 04401
 cthorn...@dahlchase.com

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RE: [Histonet] cell blocks

2011-08-02 Thread Weems, Joyce
We have a 6 hours program that we process ours on - our assistant works wee 
hours of the morning and has them ready to start around 6 am. If they don't get 
on same day, they go on the regular overnight run. j 


Joyce Weems 
Pathology Manager 
Saint Joseph's Hospital 
5665 Peachtree Dunwoody Rd NE 
Atlanta, GA 30342 
678-843-7376 - Phone 
678-843-7831 - Fax 


From: Clare Thornton cthorn...@dahlchase.com
Subject: [Histonet] cell blocks
To: 'Histonet@lists.utsouthwestern.edu' Histonet@lists.utsouthwestern.edu
Date: Tuesday, August 2, 2011, 1:14 PM


How does everyone process their cell blocks?  Currently, we use our biopsy run 
for smaller cell blocks, but the larger ones we use our routine tissue 
process.  Our lab manager would like us to look at putting all cell blocks, 
regardless of size, on our biopsy run, to increase turn around time.  I have my 
doubts, since some cell blocks, especially bronch washes and pleural fluids, 
can be quite large and greasy or mucous-y.  What does everyone else do?  We use 
standard 10% NBF, xylene, and paraplast xtra on our processors.  We would 
process on a Leica Peloris.  Our standard bx protocol is about 1.5 hours total, 
and our standard routine protocol is about 7 hours.

Thank you!

Clare J. Thornton, HTL(ASCP),QIHC
Assistant Histology Supervisor
Dahl-Chase Diagnostic Services
417 State Street, Suite 540
Bangor, ME 04401
cthorn...@dahlchase.com

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[Histonet] Perforin Ab

2011-08-02 Thread Chiriboga, Luis
Can anyone recommend a perforin ab for use in FFPE human tissue?
Thanks in advance
Luis


Luis Chiriboga Ph.D
OCS Experimental Pathology IHC Core Lab
Bellevue Hospital Center
Department of Pathology 4w27
(212) 562-4667
luis.chirib...@nyumc.org


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[Histonet] Histotech Position in Springfield, Illinois

2011-08-02 Thread Vickroy, Jim
Histotechnician
Job Description
Basic Function: Process tissue and prepare slides for diagnosis by pathologists.
Requirements for the position include:
High school graduate required.
HT(ASCP) registered or eligible
Light physical effort.
Job Location
Springfield, IL US
Position Type
Full-Time/Regular
Hours of Work
9:00 a.m. - 5:30 p.m.
Weekends (specify)
as needed
Exempt or Non-Exempt
Non-Exempt

Our careers website is www.memorialcareers.comhttp://www.memorialcareers.com

Breanne Kasprzyk│Recruitment Specialist
│Memorial Health System │701 North First Street│ Springfield, IL 62781
•: 217.788.4587│7: 217.788.5539│•kasprzyk.brea...@mhsil.com
•choosememorial.orghttp://www.memorialcareers.com/ €: 
Locationhttp://maps.google.com/maps?f=qsource=s_qhl=engeocode=q=200+West+Dodge+Street,+Springfield,+Illinois+62702sll=39.808668,-89.65569sspn=0.015396,0.03798ie=UTF8hq=hnear=200+W+Dodge+St,+Springfield,+Sangamon,+Illinois+62702ll=39.812146,-89.656141spn
Thank you for choosing Memorial!


James Vickroy BS, HT(ASCP)

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



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Re: [Histonet] uncertainity of results in histopathology

2011-08-02 Thread Tony Reilly
Hi Muhammad
 
I assume you are referring to Measurement of Uncertainty (MOU).  This is only 
used for quantitative results and not applicable to Histology processing.  The 
only times I have seen it applied in Anatomic Pathology are for Her2 and white 
cell counts on Broncho-alveolar lavages. 
 
 EM staff use grids to make measurements on specimens and of course 
Pathologists use graticules to record measurements on tissue sections.  Our 
local accreditation body has yet to make a call on these two measurements.
 
regards
Tony
 
 
 

Tony Reilly  B.App.Sc. , M.Sc.
Chief Scientist, Anatomical Pathology
Pathology Queensland-PA Laboratory
_
Clinical and Statewide Services Division| QueenslandHealth
 
Level 1, Building 15,Princess Alexandra Hospital
Ipswich Road,WOOLLOONGABBA  Qld4102
Ph: 07 3176 2412
Mob: 0402 139411
Fax: 07 3176 2930
Email: tony_rei...@health.qld.gov.au
Web:  www.health.qld.gov.au/qhcss/
 
 


 tahs...@brain.net.pk 8/2/2011 9:39 pm 
Dear all please guide me about uncertainity of results in Histopathology
at different steps,including fixation of tissue
,grossing,processing,microtomy,staining,IHC,special staining and
interpretation etc.
This is the requirement of ISO 15189 CLAUSE:5.6.2
Muhammad Tahseen
SKMCHRC
Pakistan


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[Histonet] Processing of derm specimens

2011-08-02 Thread CrochiereSteve
I have recently had a problem with my skin specimens being  
underprocessed. I use a Leica 300ASP. The schedule is as follows:
10% NBF x 2 for 1 hour ea.
80% Reagent Alcohol for 1 hour
95% Reagent Alcohol x 2 for 1 hour each
100% Reagent Alcohol for 1 hour each
Xylene x 3 for 1 hour each
Paraffin x 3 for 1 hour each
 
The specimens are mushy and swell on the ice
Any input is welcome.
 
send response to :
_scrochiere@nedlc.com_ (mailto:scrochi...@nedlc.com) 
 
thanks
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RE: [Histonet] Processing of derm specimens

2011-08-02 Thread Elizabeth Chlipala
That processing schedule should be fine for skin samples, we add an additional 
100% alcohol step so we have three absolute steps at 1 hour each (I would 
remove one 95%).  Thickness of your samples is also important they should be 
around 3mm in thickness if they are thicker than that they may not process 
properly.  The other thing is that your solutions need to be fresh for samples 
to process properly.

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, CO 80308-1592
(303) 682-3949 office
(303) 682-9060 fax
(303) 881-0763 cell
www.premierlab.com

Ship to address:

1567 Skyway Drive, Unit E
Longmont, CO 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
crochierest...@aol.com
Sent: Tuesday, August 02, 2011 4:46 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Processing of derm specimens

I have recently had a problem with my skin specimens being
underprocessed. I use a Leica 300ASP. The schedule is as follows:
10% NBF x 2 for 1 hour ea.
80% Reagent Alcohol for 1 hour
95% Reagent Alcohol x 2 for 1 hour each
100% Reagent Alcohol for 1 hour each
Xylene x 3 for 1 hour each
Paraffin x 3 for 1 hour each

The specimens are mushy and swell on the ice
Any input is welcome.

send response to :
_scrochiere@nedlc.com_ (mailto:scrochi...@nedlc.com)

thanks
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[Histonet] Reorienting frozen tissue

2011-08-02 Thread Daniela Bodemer
Hi all,

 

I would like to know if it is possible and how to reorient or reembedd
human tissue, that has been frozen at -80C in OCT. 

 

Many thanks,

 

Daniela Bodemer 

Research Assistant

Surgical Research, Infection and Immunity

 

Murdoch Childrens Research Institute

The Royal Children's Hospital

Flemington Road Parkville Victoria 3052 Australia 

T 03 9345 5930 T (03 9345 4116) 

E daniela.bode...@mcri.edu.au mailto:firstname.surn...@mcri.edu.au 

www.mcri.edu.au http://www.mcri.edu.au/ 

 

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[Histonet] Manual embedding

2011-08-02 Thread Scott Parker
Dear Histonetters:

I am interested in acquiring a pitcher and heating jacket for melting and
pouring paraffin during manual embedding. My work is relatively low volume
and in a university research lab setting so I am trying to avoid purchasing
an expensive embedding station. Can anyone recommend an honest supplier of
used histology equipment that might be able to provide me with this item?

Thank you for your expertise!

Scott L. Parker
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