RE: [Histonet] Re: Negative Controls

2014-04-30 Thread Campbell, Tasha M.
So this has confused me more. So before you would run a negative control
for each block you were testing and you would use the negative mouse or
rabbit reagent.  Now you don't have to do that but you still need a
negative tissue control.  So what exactly does this mean?  Does it mean
for every antibody that you are running you need to have a negative
tissue control for it?  So instead of using the negative mouse serum you
would run a known negative tissue control with the antibody, say CD3 or
whatever it is?  So are most people doing a control slide with a
negative tissue and a positive tissue on it?

 
 
Tasha Campbell, B.S.,HTL(ASCP)
Frederick Gastroenterology Associates
310 W. 9th St.
Frederick, MD 21701
301-695-6800 ext. 144 (w)
304-685-9307 (c)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Terri
Braud
Sent: Tuesday, April 29, 2014 1:30 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Negative Controls

On Message 7 - Negative Controls
While it is true that if you run polymers, you no longer have to run a
negative reagent control, HOWEVER, you still must have a negative tissue
control, which to quote CAP: must  show no staining of tissues known to
lack the antigen
Any of the following can serve as a negative tissue control:
1. Multi tissue blocks.  These can provide simultaneous positive and
negative tissue controls and are considered best practice...
The type of negative tissue control used (i.e. separate sections,
internal controls, or multitissue blocks) must be specified in the
laboratory manual.
Thus sayeth CAP, the almighty.  Please see ANP.22570
Our lab has defined our negative controls as a piece of Uterus as the
negative tissue in a multitissue block as a negative tissue control for
most of our antibodies, though for a few that might be too reactive in
uterus, we use a piece of skin.
I hope this helps.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

Message: 7
From: Beth Brinegar bbrinegar...@gmail.com
Subject: [Histonet] Negative controls
Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies
Appropriate negative controls are used.



-



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it was sent. It may contain information that is privileged and/or
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under applicable
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RE: [Histonet] Re: Negative Controls

2014-04-30 Thread Campbell, Tasha M.
As of now, my lab took that as you just needed one negative slide per
run.  And that negative slide is getting the negative mouse or rabbit
serum.  Is this correct?

 
 
 
Tasha Campbell, B.S.,HTL(ASCP)
Frederick Gastroenterology Associates
310 W. 9th St.
Frederick, MD 21701
301-695-6800 ext. 144 (w)
304-685-9307 (c)

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Terri
Braud
Sent: Tuesday, April 29, 2014 1:30 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Negative Controls

On Message 7 - Negative Controls
While it is true that if you run polymers, you no longer have to run a
negative reagent control, HOWEVER, you still must have a negative tissue
control, which to quote CAP: must  show no staining of tissues known to
lack the antigen
Any of the following can serve as a negative tissue control:
1. Multi tissue blocks.  These can provide simultaneous positive and
negative tissue controls and are considered best practice...
The type of negative tissue control used (i.e. separate sections,
internal controls, or multitissue blocks) must be specified in the
laboratory manual.
Thus sayeth CAP, the almighty.  Please see ANP.22570
Our lab has defined our negative controls as a piece of Uterus as the
negative tissue in a multitissue block as a negative tissue control for
most of our antibodies, though for a few that might be too reactive in
uterus, we use a piece of skin.
I hope this helps.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

Message: 7
From: Beth Brinegar bbrinegar...@gmail.com
Subject: [Histonet] Negative controls
Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies
Appropriate negative controls are used.



-



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it was sent. It may contain information that is privileged and/or
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under applicable
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[Histonet] PT

2014-04-30 Thread Campbell, Tasha M.
I need to enroll in a Proficiency testing program just for the technical
part.  I am looking for the cheapest program that CLIA would recognize.
I am only CLIA certified.  

 

Thanks.

 

 

 

 

Tasha Campbell, B.S.,HTL(ASCP)

Frederick Gastroenterology Associates

310 W. 9th St.

Frederick, MD 21701

301-695-6800 ext. 144 (w)

304-685-9307 (c)

 

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RE: [Histonet] Re: Negative Controls

2014-04-30 Thread Sebree Linda A
Tasha,

We use the negative elements within our patient sample as our negative tissue 
control.

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

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Campbell, Tasha 
M.
Sent: Wednesday, April 30, 2014 6:48 AM
To: Terri Braud; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Negative Controls

So this has confused me more. So before you would run a negative control for 
each block you were testing and you would use the negative mouse or rabbit 
reagent.  Now you don't have to do that but you still need a negative tissue 
control.  So what exactly does this mean?  Does it mean for every antibody that 
you are running you need to have a negative tissue control for it?  So instead 
of using the negative mouse serum you would run a known negative tissue control 
with the antibody, say CD3 or whatever it is?  So are most people doing a 
control slide with a negative tissue and a positive tissue on it?

 
 
Tasha Campbell, B.S.,HTL(ASCP)
Frederick Gastroenterology Associates
310 W. 9th St.
Frederick, MD 21701
301-695-6800 ext. 144 (w)
304-685-9307 (c)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Terri Braud
Sent: Tuesday, April 29, 2014 1:30 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Negative Controls

On Message 7 - Negative Controls
While it is true that if you run polymers, you no longer have to run a negative 
reagent control, HOWEVER, you still must have a negative tissue control, which 
to quote CAP: must  show no staining of tissues known to lack the antigen
Any of the following can serve as a negative tissue control:
1. Multi tissue blocks.  These can provide simultaneous positive and negative 
tissue controls and are considered best practice...
The type of negative tissue control used (i.e. separate sections, internal 
controls, or multitissue blocks) must be specified in the laboratory manual.
Thus sayeth CAP, the almighty.  Please see ANP.22570 Our lab has defined our 
negative controls as a piece of Uterus as the negative tissue in a multitissue 
block as a negative tissue control for most of our antibodies, though for a few 
that might be too reactive in uterus, we use a piece of skin.
I hope this helps.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

Message: 7
From: Beth Brinegar bbrinegar...@gmail.com
Subject: [Histonet] Negative controls
Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies 
Appropriate negative controls are used.



-



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This E-Mail is intended only for the use of the individual or entity to which 
it was sent. It may contain information that is privileged and/or confidential, 
and the use or disclosure of such information may also be restricted under 
applicable federal and state law. If you received this communication in error, 
please do not distribute any part of it or retain any copies, and delete the 
original E-Mail.
Please notify the sender of any error by E-Mail.

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RE: [Histonet] Re: Negative Controls

2014-04-30 Thread Martha Ward-Pathology
So do we.

 
Martha Ward, MT (ASCP) QIHC
Manager

Molecular Diagnostics Lab
Medical Center Boulevard  \  Winston-Salem, NC 27157
p 336.716.2109  \  f 336.716.5890  
mw...@wakehealth.edu  
 
 



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sebree Linda A
Sent: Wednesday, April 30, 2014 8:35 AM
To: 'Campbell, Tasha M.'; Terri Braud; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Negative Controls

Tasha,

We use the negative elements within our patient sample as our negative tissue 
control.

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

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Campbell, Tasha 
M.
Sent: Wednesday, April 30, 2014 6:48 AM
To: Terri Braud; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Negative Controls

So this has confused me more. So before you would run a negative control for 
each block you were testing and you would use the negative mouse or rabbit 
reagent.  Now you don't have to do that but you still need a negative tissue 
control.  So what exactly does this mean?  Does it mean for every antibody that 
you are running you need to have a negative tissue control for it?  So instead 
of using the negative mouse serum you would run a known negative tissue control 
with the antibody, say CD3 or whatever it is?  So are most people doing a 
control slide with a negative tissue and a positive tissue on it?

 
 
Tasha Campbell, B.S.,HTL(ASCP)
Frederick Gastroenterology Associates
310 W. 9th St.
Frederick, MD 21701
301-695-6800 ext. 144 (w)
304-685-9307 (c)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Terri Braud
Sent: Tuesday, April 29, 2014 1:30 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Negative Controls

On Message 7 - Negative Controls
While it is true that if you run polymers, you no longer have to run a negative 
reagent control, HOWEVER, you still must have a negative tissue control, which 
to quote CAP: must  show no staining of tissues known to lack the antigen
Any of the following can serve as a negative tissue control:
1. Multi tissue blocks.  These can provide simultaneous positive and negative 
tissue controls and are considered best practice...
The type of negative tissue control used (i.e. separate sections, internal 
controls, or multitissue blocks) must be specified in the laboratory manual.
Thus sayeth CAP, the almighty.  Please see ANP.22570 Our lab has defined our 
negative controls as a piece of Uterus as the negative tissue in a multitissue 
block as a negative tissue control for most of our antibodies, though for a few 
that might be too reactive in uterus, we use a piece of skin.
I hope this helps.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

Message: 7
From: Beth Brinegar bbrinegar...@gmail.com
Subject: [Histonet] Negative controls
Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies 
Appropriate negative controls are used.



-



CONFIDENTIALITY NOTICE:

This E-Mail is intended only for the use of the individual or entity to which 
it was sent. It may contain information that is privileged and/or confidential, 
and the use or disclosure of such information may also be restricted under 
applicable federal and state law. If you received this communication in error, 
please do not distribute any part of it or retain any copies, and delete the 
original E-Mail.
Please notify the sender of any error by E-Mail.

Thank you for your cooperation.


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RE: [Histonet] Re: Negative Controls

2014-04-30 Thread Weems, Joyce K.
So do we

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

This e-mail, including any attachments is the property of Saint Joseph's 
Hospital and is intended for the sole use of the intended recipient(s).  It may 
contain information that is privileged and confidential.  Any unauthorized 
review, use, disclosure, or distribution is prohibited. If you are not the 
intended recipient, please delete this message, and reply to the sender 
regarding the error in a separate email.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sebree Linda A
Sent: Wednesday, April 30, 2014 8:35 AM
To: 'Campbell, Tasha M.'; Terri Braud; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Negative Controls

Tasha,

We use the negative elements within our patient sample as our negative tissue 
control.

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

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Campbell, Tasha 
M.
Sent: Wednesday, April 30, 2014 6:48 AM
To: Terri Braud; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Negative Controls

So this has confused me more. So before you would run a negative control for 
each block you were testing and you would use the negative mouse or rabbit 
reagent.  Now you don't have to do that but you still need a negative tissue 
control.  So what exactly does this mean?  Does it mean for every antibody that 
you are running you need to have a negative tissue control for it?  So instead 
of using the negative mouse serum you would run a known negative tissue control 
with the antibody, say CD3 or whatever it is?  So are most people doing a 
control slide with a negative tissue and a positive tissue on it?



Tasha Campbell, B.S.,HTL(ASCP)
Frederick Gastroenterology Associates
310 W. 9th St.
Frederick, MD 21701
301-695-6800 ext. 144 (w)
304-685-9307 (c)
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Terri Braud
Sent: Tuesday, April 29, 2014 1:30 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Negative Controls

On Message 7 - Negative Controls
While it is true that if you run polymers, you no longer have to run a negative 
reagent control, HOWEVER, you still must have a negative tissue control, which 
to quote CAP: must  show no staining of tissues known to lack the antigen
Any of the following can serve as a negative tissue control:
1. Multi tissue blocks.  These can provide simultaneous positive and negative 
tissue controls and are considered best practice...
The type of negative tissue control used (i.e. separate sections, internal 
controls, or multitissue blocks) must be specified in the laboratory manual.
Thus sayeth CAP, the almighty.  Please see ANP.22570 Our lab has defined our 
negative controls as a piece of Uterus as the negative tissue in a multitissue 
block as a negative tissue control for most of our antibodies, though for a few 
that might be too reactive in uterus, we use a piece of skin.
I hope this helps.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

Message: 7
From: Beth Brinegar bbrinegar...@gmail.com
Subject: [Histonet] Negative controls
Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies 
Appropriate negative controls are used.



-



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This E-Mail is intended only for the use of the individual or entity to which 
it was sent. It may contain information that is privileged and/or confidential, 
and the use or disclosure of such information may also be restricted under 
applicable federal and state law. If you received this communication in error, 
please do not distribute any part of it or retain any copies, and delete the 
original E-Mail.
Please notify the sender of any error by E-Mail.

Thank you for your cooperation.


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This e-mail message (including 

[Histonet] Special stain control validation- CAP compliance

2014-04-30 Thread Stacy McLaughlin

Hello,
We validate our control blocks prior to patient use.  We label the slide with 
the stain, date, and results.  We keep the slides in a file for reference.  Our 
recent CAP inspection cited us on this because it was not documented on paper.  
I am considering challenging this, as I feel what we're doing meets the intent 
of the checklist question.
What are your opinions?
Thanks,
Stacy

**NEW** 07/29/2013
ANP.21460 Special Stain Controls Phase I
Validated tissue controls are required for each special stain.
NOTE: Positive tissue controls assess the performance of the special stain. 
Special stains are
performed on sections of control tissue known to contain components specific to 
each special stain.
Validation of tissue used as a positive control must be performed and 
documented before being
used with clinical specimens.
Evidence of Compliance:
✓ Written results of special stain control tissue validation
[Cooley-Dickinson.org]
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Re: [Histonet] Question about high complexity testing for histotechnologists

2014-04-30 Thread Rene J Buesa
NO, because the license in histotechnology INCLUDES high complexity testing. 
On the other hand there are some tests like FISH with the VYSIS system that 
requires a special training with its own certification.
René J. 
On Tuesday, April 29, 2014 10:15 PM, Delia, Catherine deli...@uhnj.org 
wrote:
  
Does anyone know if there is a regulatory agency that requires high complexity 
testing certification for histotechnologists.

Catherine Susan Delia, BS. HT. ASCP
Chief Technologist, Anatomic Pathology
University Hospital
150 Bergen Street
E-151
Newark, New Jersey 07103
Phone: 973-972-5717
Cell: 908-391-1060
Fax: 973-972-5724
deli...@uhnj.orgmailto:deli...@uhnj.org

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[Histonet] RE: CAP question ANP.22978 - Her2 assay validation

2014-04-30 Thread Vanessa Perez
https://www.biomax.us/tissue-arrays/Breast/

theres the link, they have various kinds, so just choose the one that comes 
with the IHC results



Vanessa Perez Garcia
Pathology Reference Lab
210-892-3746
210-892-3732
vpe...@pathreflab.com

-Original Message-
From: Martha Ward-Pathology [mailto:mw...@wakehealth.edu] 
Sent: Wednesday, April 30, 2014 7:11 AM
To: Vanessa Perez
Subject: RE: CAP question ANP.22978 - Her2 assay validation

Thanks.   I like the idea of the microarray slide as well.   Where did you 
purchase your slide?

martha

-Original Message-
From: Vanessa Perez [mailto:vpe...@pathreflab.com] 
Sent: Tuesday, April 29, 2014 5:18 PM
To: Martha Ward-Pathology; histonet@lists.utsouthwestern.edu
Subject: RE: CAP question ANP.22978 - Her2 assay validation

From what I have read and understand you should be able to do a write up the 
retroactive review based on the PT results.  What we did here was bought a 
microarray slide that came with the HER2/ER/PR results, ran them on our 
machine, and compared our results to the ones that came with the slide.


Vanessa Perez Garcia
Pathology Reference Lab
210-892-3746
210-892-3732
vpe...@pathreflab.com

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Martha 
Ward-Pathology
Sent: Tuesday, April 29, 2014 2:47 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] CAP question ANP.22978 - Her2 assay validation

Hello all,

I have been reading through the most recent revisions and want to see how 
others are handling this question.   The explanation states that it is for new 
and existing assays and that if your validation does not meet current standards 
that you must supplement and bring it into compliance.  Furthermore if you do 
not have any documentation from the initial validation the assay must be fully 
revalidated and documented.

Our lab has been performing the Herceptest from Dako (FDA approved) since 
before 2008 and participating in the HER2 proficiency testing since it was 
first offered.   We have our statistical results comparing our IHC patient 
results to FISH Her2 results since 2008 and we have always done well on our CAP 
proficiency testing (95%-100%).We do inter-pathologist result comparisons, 
using know CAP slides and have 95% to 100% agreements.   

What I do not have however is the original results of the slides that were 
stained to set up the original assay.   Under these circumstances will we need 
to completely revalidate the assay, using the mandated 20+/20- cases, or can we 
simply do a retroactive formal review and write up of our past performances on 
our proficiency testing challenges?

Thanks in advance for your help with this!

 
Martha Ward, MT (ASCP) QIHC
Manager
 
Molecular Diagnostics Lab
Medical Center Boulevard  \  Winston-Salem, NC 27157


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[Histonet] Thank You!

2014-04-30 Thread Jennifer Oskins
All-

   A very sincere thank you to everyone who has responded so
graciously to my request for information for Seventh Wave Pathology and for
additional suggestions for CRO Histology/Pathology services. I have
forwarded the information on. Thank you again for the great feedback!

Jennifer
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[Histonet] animal human biopsies

2014-04-30 Thread Davis, Cassie
Some threw the thought of processing biopsies from veterinary clinics as a way 
of increasing outpatient volumes. I am concerned there may be a regulation 
against this. Does anybody know of any?

Cassandra Davis
cda...@che-east.org
302-575-8095



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[Histonet] Formalin fixation problems

2014-04-30 Thread Frances Pearsall
Recently we started having problems with our 10% nb formalin not completely 
fixing our animal tissues.  We haven't done any thing different in making up 
the solutions, but we're finding incomplete fixation in the center of the 
tissues. We are letting it stay in formalin the same amount of time (24-48 hrs) 
 as we've always done. The pH has not changed. Does any one have any 
suggestions as to where we can look to trouble shoot correcting this problem?

Our recipe method is: 4g Sodium Phosphate, monobasic monohydrate(Fisher 
Chemical co.)  6.5g Sodium Phosphate, dibasic anhydrous(EMD Chemical co.) 37% 
Formaldehyde(EMD Chem.co.)   10 parts formaldehyde to 90 parts Dh20.   Any 
helpful thoughts would be appreciated.



Thank you,  Fran Pearsall HT
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[Histonet] Is there a way to post pictures of slides on histonet? Or to make them available for people to look at?

2014-04-30 Thread Lewis, Patrick
Hi everyone,

What is a good way to post pictures of slides for you guys to look at?

I had a weird black precipitate in one of my IHCs and I'd like for you guys to 
look at them and see if you recognize what this artifact is?

Thanks

Patrick.

PS: I tried uploading them as attachments but the size was too large even 
though I tried to crop things to keep the size to a minimum.

Thanks

Patrick.


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[Histonet] Is there a way to post pictures of slides on histonet? Or to make them available for people to look at?

2014-04-30 Thread Shirley A. Powell
HI Patrick, Marvin Hanna posted these instructions in the below message on 
histonet yesterday.  This is a good way to post images you wish to discuss on 
histonet.  He has made available a way to do this for the histonet community, 
as well as has the archives of histonet on the www.histosearch.com website.  
You cannot post images on histonet. 

Shirley Powell


 Hi Histonetters,

 Tim Morken asked me about posting images for discussion on Histonet a couple 
 of weeks ago and we noticed our images website is no longer running. As we 
 move into digital pathology, having the ability to post images to discuss on 
 Histonet is important. So, we set up an easy way to post images for Histonet 
 on Histosearch at http://histosearch.com/imageupload/. You need to fill in 
 your name, a title for your images, select images to upload from your 
 computer or smartphone and click submit. There is no need to register and it 
 takes about 2 minutes. We intentionally did not include comments on the 
 website so the discussions will take place on Histonet.

 We have also set up mobile pages for searching Histosearch and the archives 
 at http://m.histosearch.com and http://m.histosearch.com/histonet/ for 
 histologists on the go. You may also want to try out the new image searching 
 capabilities on Histosearch. After searching with keyword(s) such as ki67 or 
 alcian blue, there is a link at the top of the results page for images.
 Clicking this will provide images related to your keyword(s) from the over 12 
 million histopathology related pages searched in Histosearch. We believe we 
 have the largest list of histology educational resources on the internet at 
 Histosearch and they are searchable for text and images.
 Let us know if we've missed any histology resources.

 Best Regards,

 Marvin Hanna


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lewis, Patrick
Sent: Wednesday, April 30, 2014 1:43 PM
To: 'Histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Is there a way to post pictures of slides on histonet? Or 
to make them available for people to look at?

Hi everyone,

What is a good way to post pictures of slides for you guys to look at?

I had a weird black precipitate in one of my IHCs and I'd like for you guys to 
look at them and see if you recognize what this artifact is?

Thanks

Patrick.

PS: I tried uploading them as attachments but the size was too large even 
though I tried to crop things to keep the size to a minimum.

Thanks

Patrick.


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

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Re: [Histonet] Is there a way to post pictures of slides on histonet? Or to make them available for people to look at?

2014-04-30 Thread Marvin Hanna

Hi Patrick,

You can upload images for Histonet at 
http://histosearch.com/imageupload/. The Histonet listserver does not 
allow attachments to messages to prevent the spread of malware. Let me 
know if you have any problems.


Best Regards,

Marvin Hanna

On 04/30/2014 01:43 PM, Lewis, Patrick wrote:

Hi everyone,

What is a good way to post pictures of slides for you guys to look at?

I had a weird black precipitate in one of my IHCs and I'd like for you guys to 
look at them and see if you recognize what this artifact is?

Thanks

Patrick.

PS: I tried uploading them as attachments but the size was too large even 
though I tried to crop things to keep the size to a minimum.

Thanks

Patrick.


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

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[Histonet] I just posted 2 photos to histosearch

2014-04-30 Thread Lewis, Patrick
Thanks everyone,

I just posted 2 images to histo search.  IS there a way to post up to 5 pics at 
once?  It looked like it suggested that you could post up to  5 pics as a group 
but I didn't see HOW to do it.

Anyway,  I have one post of outside of the tissue area, and one post of the 
tissue area.

What is this weird black precipitate?  I was using Red AEC as a substrate.

Patrick.


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[Histonet] Awards Spotlight - The Newcomer Helping Hand Award

2014-04-30 Thread Elizabeth Chlipala
Award Spotlight - The Newcomer Helping Hand Award
This award is sponsored by Newcomer Supply Inc. and consist of a $1500.00 
grant. This is a new award for the NSH it has only been given out once so far, 
last year was the first year it was given and Jean Mitchell NSH's Region IV 
director was its first recipient.  Jean knows first-hand what it's like to help 
others internationally she was able to travel to Botswana, Africa in August 
2013 as part of an ASCP Laboratory Mission to assess and teach good 
histotechnology practices in Botswana.
This grant is intended to:
Support national and or international histology education outreach efforts.  
Increase the quality and expertise of histology educational opportunities for 
student groups with limited or deteriorated access to educational facilities 
and educators.  Affect efforts to recruit future generations of 
histotechnologists and promote the study of histology.   Provide needed 
educational supplies or equipment.
This grant can be used to support any educational opportunity such as hosting 
high school students in your laboratory or at a STEM event.  Nominate yourself 
if you are planning such an event or a colleague if you know that they have 
been involved in educational opportunities in the past and are planning to do 
so in the future at the following link 
http://nsh.org/scholarships-awards/advocacy/service%20awards?nid=2930  This is 
just one way that this award can be used.
Helping others both nationally and internationally learn about histology can be 
a really fun experience.  We host students yearly in our lab and it is an 
exhausting but very rewarding experience.  Getting our young students 
interested in science is in my opinion is a really worthy cause especially if I 
can do that by teaching them about histology.
Liz

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

March 10, 2014 is Histotechnology Professionals Day

Ship to Address:

Premier Laboratory, LLC
1567 Skyway Drive, Unit E
Longmont, CO 80504

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Re: [Histonet] I just posted 2 photos to histosearch

2014-04-30 Thread Marvin Hanna

Hi Patrick,

To post more than one image, there is a link under choose file where 
you uploaded the first picture for add another image. When you click 
add another image, it opens up another choose file box for a second 
image to upload. Or you can just post them one at a time if you like.


I've seen that black precipitate on slides in an IHC lab I was at a 
couple of years ago. If I remember correctly, we thought it was a 
formalin-heme pigment which can be caused when formalin is acidic (not 
buffered).


Marvin

On 04/30/2014 02:05 PM, Lewis, Patrick wrote:

Thanks everyone,

I just posted 2 images to histo search.  IS there a way to post up to 5 pics at 
once?  It looked like it suggested that you could post up to  5 pics as a group 
but I didn't see HOW to do it.

Anyway,  I have one post of outside of the tissue area, and one post of the 
tissue area.

What is this weird black precipitate?  I was using Red AEC as a substrate.

Patrick.


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

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[Histonet] gmed/ggastro interfacing with pathology for seamless transition?

2014-04-30 Thread Sophia Lin
Hi all,

Our practice is moving forward to bringing in-house pathology since we
already have in-house histology. Any gastro practices that use gmed/ggastro
and have a seamless pathology module that can be added for a smooth
transition? This would entail using ggastro/gmed and interfacing with the
pathology module. We currently use WINSURGE but cannot interface with
ggmed/gastro easily.

Any thoughts?

Thanks,
Sophia
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