Re: [Histonet] thermometer

2011-04-19 Thread V. Neubert
A pyrometer should do the job, I guess.
 My last CLIA inspection, I was told to check the temperature in the wax
 chamber of my embedding station to compare against the temperature it
 says it is...does anyone know of a good thermometer to purchase?



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Re: [Histonet] Question about delayed start in Leica Tissue Processor

2011-04-19 Thread Louise Renton
The easiest way to remember is to count the midnights between starting and
ending - therefore today will be 0, tomorrow 1etc

On Mon, Apr 18, 2011 at 6:24 PM, Jenny Vega histotech...@gmail.com wrote:

 Yes, that is what makes sense to me. Tomorrow morning after removing the
 specimens from the tissue basket I will check how my supervisor set the
 clock last Friday. If she chose 3-18:20, then by logic I will have to chose
 4-18:20, since I will be away for the holidays  for 4 days straight and I
 need the tissues to be processed by the next monday (april 25). I was told
 that the tissue processor starts at 6pm and it is done the next morning. I
 did not understood military time before and now I know that 18:20 means
 6:20pm.

 Thanks

 On Mon, Apr 18, 2011 at 8:39 AM, Thomas, Nancy n...@stowers.org wrote:

  We have the same processor.  If you are returning to work next Monday
  morning, then you would choose the 4 day delay.  It would begin
 processing
  at 18:20 Sunday night and be ready on Monday morning.
  Nancy Thomas
  Stowers Institute
 
  -Original Message-
  From: histonet-boun...@lists.utsouthwestern.edu [mailto:
  histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jenny Vega
  Sent: Sunday, April 17, 2011 8:52 PM
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] Question about delayed start in Leica Tissue
 Processor
 
  Hello. I have little experience using the tissue processor from my lab
  which is an old version of the Leica  TP1020. I was taugh that since on
  weekends the processor is not going to be used then you have to set up
 the
  days of delay for example 2-18:20 (2 represents saturday and sunday). On
  Monday
  (tomorrow) I have the day off, so the processor won't be used. When I
 come
  back on Tuesday I have to change the the time as 0-18:20 so that the
  processor starts working that day and on wednesday. On thursday, friday,
  saturday and Sunday will also have the days off. I am confused because my
  supevisor told me to set the time as 3-18:20 next Wednesday, and since I
  will not be working in the lab for 4 days straight that does not make
 sense,
  it is suppose to be 4-18:20 instead. I think she made a mistake telling
 me
  that since maybe she confused the program of this week when the processor
  was programmed as 3-18:20 because used for 3 days straight (saturday to
  monday). My supervisor won't be in the lab next week so I cannot ask her.
 
  This question seems silly but I want to be sure. I know that if tissue is
  left for a long time in paraffin the tissue can get over-harden and I
 don't
  want to program de delayed start as 3-18:20 thinking it is the correct
 way
  when is not.
 
  Thanks
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-- 
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Bone Research Unit
University of the Witwatersrand
Johannesburg
South Africa
+27 11 717 2298 (tel  fax)
073 5574456 (emergencies only)
There are nights when the wolves are silent and only the moon howls.
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No trees were killed in the sending of this message.
However, many electrons were terribly inconvenienced.
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[Histonet] Tissue adhesion to slides

2011-04-19 Thread Abbey Mortimer
Hello out there!

I was wondering if any of you have experience in attaching human retinae 
(~250-300 microns thick) to slides for manual immunohistochemistry. Starfrost 
does not seem adequate.

Any advice would be greatly appreciated!
Regards,
Abbey


Abbey Mortimer
PhD Candidate
School of Psychological Science
La Trobe University
Bundoora, Victoria, 3083
AUSTRALIA

Phone: (03) 9479 2470
Email: a.morti...@latrobe.edu.au

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[Histonet] Cytotech job opening in Brooklyn NY

2011-04-19 Thread Eric Sulkosky
There is a full time position open for a Cytotechnologist in Brooklyn, NY. A
candidate with Histology background is preferred. Please forward letter of
interest and resume to



Ellen Barbarino

ebarbar...@siradonc.com



Thanks
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[Histonet] Neuronal staining mouse limb sections

2011-04-19 Thread Hendrik Mommaerts
Hello, 

 

I'm investigating a potential neuronal defect  of our transgenic mouse
embryos.

 

Until now the staining I tried (luxol Fast Blue) didn't work out.

 

I was wondering now if there is an alternative for this.

Is there a staining (or an Ab), that I can use to detect any kind of neurons
in the limb of a mouse embryo?

 

I'm looking for a general detection of neurons.

 

Preferentially I would like it to work on frozen sections, but for now
anything would work for me!

 

Thank you!

 

 

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RE: [Histonet] Neuronal staining mouse limb sections

2011-04-19 Thread Anatoli Gleiberman
Hi Hendrik,
Try rabbit neuro-specific beta-III tubulin antibody (Abcam ab18207). Works fine 
on frozen and paraffin sections.

Anatoli Gleiberman, PhD
Director of Histopathology
Cleveland Biolabs, Inc
73 High Street
Buffalo, NY 14203
phone:716-849-6810 ext.354
fax:716-849-6817
e-mail: agleiber...@cbiolabs.com

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Hendrik 
Mommaerts
Sent: Tuesday, April 19, 2011 9:51 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Neuronal staining mouse limb sections

Hello, 

 

I'm investigating a potential neuronal defect  of our transgenic mouse
embryos.

 

Until now the staining I tried (luxol Fast Blue) didn't work out.

 

I was wondering now if there is an alternative for this.

Is there a staining (or an Ab), that I can use to detect any kind of neurons
in the limb of a mouse embryo?

 

I'm looking for a general detection of neurons.

 

Preferentially I would like it to work on frozen sections, but for now
anything would work for me!

 

Thank you!

 

 

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[Histonet] IHC on frozen sections

2011-04-19 Thread Jane C. Moose
Following is question on behalf of   Jana Moose Ritter, DVM
janamo...@yahoo.com

 

 

We are going to perform IHC on frozen sections, and the tissues  (pig
aorta)  will be harvested on a Friday.

 

Histo lab is wondering:

 

1) can tissue fix in paraformaldehyde over the weekend until next steps
(sucrose and frozen embedding to be completed on Monday) 

2) can fixative be switched to sucrose at the end of Friday (tissue
would remain in sucrose until frozen embedding on Monday)

3) must complete the solution switch and entire frozen embedding process
on Saturday

 

 

Thanks for your help. 

 

Jane Moose

LIS Coordinator

Newberry County Memorial Hospital

Newberry, SC  29108

P-803-405-7129

F- 803-405-7474

 

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[Histonet] Question

2011-04-19 Thread Carmen Maria Garcia Pascual

Good afternoon:

I am Carmen Garcia a PhD student from the Faculty of medicine from the 
University of Valencia.We work with cryocut of mouse ovary, now I want 
to see the filopodia of the endothelial cells, do you have any 
suggestion about what I should do?
Thank you so much,

Carmen


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[Histonet] Miller's Elastin Stain

2011-04-19 Thread Malika Benatti
** Proprietary **
** Reply Requested When Convenient **

Hi there,

Does anyone use commercial Miller's Elastic Stain other than VWR Ref 35115S one 
 ?
If so I would be grateful if you could let me know which one you use
Thanks in advance 

Malika



Malika Benatti
 
Specialist BMS 
Camelia Botnar Laboratories
Histopathology Department
Great Ormond Street Hospital
London WC1N 3JH

 
Tel:  +44 20 7405 9200 ext 5475
Fax:  +44 20 7829 7875
 
ben...@gosh.nhs.uk


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This message may contain confidential information. If you are not the intended 
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Please do not disclose, copy or distribute information in this e-mail or take 
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Thank you for your co-operation.

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[Histonet] RE: [IHCRG] Ventana EBER DNP

2011-04-19 Thread Sheila Fonner
SAME HERE!!!  I would love some help with this.  We are going to start doing
the EBER with Ventana and have no idea where to start.

 

Thanks in advance for ANY suggestions or  help you could give.

 

Sheila, HT (ASCP)

KDL Pathology

Knoxville, TN

 

 

From: ih...@googlegroups.com [mailto:ih...@googlegroups.com] On Behalf Of
Tallardy, Betty S
Sent: Tuesday, April 19, 2011 10:55 AM
To: ih...@googlegroups.com
Subject: [IHCRG] Ventana EBER DNP

 

Hi Group,

Is anyone stuck in the EBER transition with Ventanas' 

 probe changeover? The new product is supplied in a small vial and of course
there are no suggestions about how to use the product. 

If anyone has some ideas on how to proceed with this, I would really
appreciate some suggestions.

I hate to waste such a pricey product trying to get something workable.

Thanks in advance.

Betty Tallardy, HT(ASCP)QIHC

Dept. of Pathology

Presbyterian Hospital

200 Hawthorne Lane

Charlotte, NC 28204

704-384-5490

bstalla...@novanthealth.org

  _  

This message and any included attachments are from NOVANT HEALTH INC. and
are intended only for the addressee(s). The information contained herein may
include trade secrets or privileged or otherwise confidential information.
Unauthorized review, forwarding, printing, copying, distributing, or using
such information is strictly prohibited and may be unlawful. If you received
this message in error, or have reason to believe you are not authorized to
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disparaging or harassing or if you find it objectionable please contact
Novant Health, Inc. at 1-800-350-0094 or forward the e-mail to
repo...@novanthealth.org. Thank you. 

-- 
You received this message because you are subscribed to the Google
Groups ihcrg group. The IHC Resource Group is a standing committee within
the National Society for Histotechnology.
 
To post to this group, send email to ih...@googlegroups.com
To unsubscribe from this group, send email to
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For more options, visit this group at
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To contact the National Society for Histotechnology, email: hi...@nsh.org or
call 443.535.4060.

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Re: [Histonet] RE: [IHCRG] Ventana EBER DNP

2011-04-19 Thread Mark Tarango
If anyone has the catalog numbers for the probes, that would help.  I
couldn't get this info from Ventana when I asked.  They said we have to ask
another lab, even for catalog numbers!

Mark

On Tue, Apr 19, 2011 at 7:59 AM, Sheila Fonner sfon...@labpath.com wrote:

 SAME HERE!!!  I would love some help with this.  We are going to start
 doing
 the EBER with Ventana and have no idea where to start.



 Thanks in advance for ANY suggestions or  help you could give.



 Sheila, HT (ASCP)

 KDL Pathology

 Knoxville, TN





 From: ih...@googlegroups.com [mailto:ih...@googlegroups.com] On Behalf Of
 Tallardy, Betty S
 Sent: Tuesday, April 19, 2011 10:55 AM
 To: ih...@googlegroups.com
 Subject: [IHCRG] Ventana EBER DNP



 Hi Group,

 Is anyone stuck in the EBER transition with Ventanas'

  probe changeover? The new product is supplied in a small vial and of
 course
 there are no suggestions about how to use the product.

 If anyone has some ideas on how to proceed with this, I would really
 appreciate some suggestions.

 I hate to waste such a pricey product trying to get something workable.

 Thanks in advance.

 Betty Tallardy, HT(ASCP)QIHC

 Dept. of Pathology

 Presbyterian Hospital

 200 Hawthorne Lane

 Charlotte, NC 28204

 704-384-5490

 bstalla...@novanthealth.org

  _

 This message and any included attachments are from NOVANT HEALTH INC. and
 are intended only for the addressee(s). The information contained herein
 may
 include trade secrets or privileged or otherwise confidential information.
 Unauthorized review, forwarding, printing, copying, distributing, or using
 such information is strictly prohibited and may be unlawful. If you
 received
 this message in error, or have reason to believe you are not authorized to
 receive it, please promptly delete this message and notify the sender by
 e-mail. If you believe that any information contained in this message is
 disparaging or harassing or if you find it objectionable please contact
 Novant Health, Inc. at 1-800-350-0094 or forward the e-mail to
 repo...@novanthealth.org. Thank you.

 --
 You received this message because you are subscribed to the Google
 Groups ihcrg group. The IHC Resource Group is a standing committee within
 the National Society for Histotechnology.

 To post to this group, send email to ih...@googlegroups.com
 To unsubscribe from this group, send email to
 ihcrg+unsubscr...@googlegroups.com
 For more options, visit this group at
 http://groups.google.com/group/ihcrg?hl=en

 To contact the National Society for Histotechnology, email: histo@nsh.orgor
 call 443.535.4060.

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Re: [Histonet] RE: [IHCRG] Ventana EBER DNP

2011-04-19 Thread Angela Bitting
Your sales rep should supply these to you.
 
I'm having problems with filling my ISH Probe Kit. I logged in my EBER Probe. I 
registered the Probe kit and went to fill it and it only lets me pick from my 
Fillable Reagents list, not the Fillable probes list. Tech support can't figure 
out why this is happening and said they haven't encountered this problem with 
any other clients. Anyone else having this issue?

 Mark Tarango marktara...@gmail.com 4/19/2011 11:08 AM 
If anyone has the catalog numbers for the probes, that would help.  I
couldn't get this info from Ventana when I asked.  They said we have to ask
another lab, even for catalog numbers!

Mark

On Tue, Apr 19, 2011 at 7:59 AM, Sheila Fonner sfon...@labpath.com wrote:

 SAME HERE!!!  I would love some help with this.  We are going to start
 doing
 the EBER with Ventana and have no idea where to start.



 Thanks in advance for ANY suggestions or  help you could give.



 Sheila, HT (ASCP)

 KDL Pathology

 Knoxville, TN





 From: ih...@googlegroups.com [mailto:ih...@googlegroups.com] On Behalf Of
 Tallardy, Betty S
 Sent: Tuesday, April 19, 2011 10:55 AM
 To: ih...@googlegroups.com 
 Subject: [IHCRG] Ventana EBER DNP



 Hi Group,

 Is anyone stuck in the EBER transition with Ventanas'

  probe changeover? The new product is supplied in a small vial and of
 course
 there are no suggestions about how to use the product.

 If anyone has some ideas on how to proceed with this, I would really
 appreciate some suggestions.

 I hate to waste such a pricey product trying to get something workable.

 Thanks in advance.

 Betty Tallardy, HT(ASCP)QIHC

 Dept. of Pathology

 Presbyterian Hospital

 200 Hawthorne Lane

 Charlotte, NC 28204

 704-384-5490

 bstalla...@novanthealth.org 

  _

 This message and any included attachments are from NOVANT HEALTH INC. and
 are intended only for the addressee(s). The information contained herein
 may
 include trade secrets or privileged or otherwise confidential information.
 Unauthorized review, forwarding, printing, copying, distributing, or using
 such information is strictly prohibited and may be unlawful. If you
 received
 this message in error, or have reason to believe you are not authorized to
 receive it, please promptly delete this message and notify the sender by
 e-mail. If you believe that any information contained in this message is
 disparaging or harassing or if you find it objectionable please contact
 Novant Health, Inc. at 1-800-350-0094 or forward the e-mail to
 repo...@novanthealth.org. Thank you.

 --
 You received this message because you are subscribed to the Google
 Groups ihcrg group. The IHC Resource Group is a standing committee within
 the National Society for Histotechnology.

 To post to this group, send email to ih...@googlegroups.com 
 To unsubscribe from this group, send email to
 ihcrg+unsubscr...@googlegroups.com 
 For more options, visit this group at
 http://groups.google.com/group/ihcrg?hl=en 

 To contact the National Society for Histotechnology, email: histo@nsh.orgor 
 call 443.535.4060.

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[Histonet] [Histonet Biopsy Program for Sakura VIP 5/6 Processor

2011-04-19 Thread Mayer,Toysha N
Try to eliminate one of the 100% Alcohols.  If it cannot eliminate it, then 
just pump it in and out.
Microwave processing actually uses Ethanol, Isopropyl, and paraffin only.


Toysha N. Mayer, MBA, HT (ASCP)
Education Coordinator
Program in Histotechnology
School of Health Professions
MD Anderson Cancer Center
(713) 563-3481
tnma...@mdanderson.org


 Message: 8
 Date: Tue, 12 Apr 2011 14:57:18 -0400
 From: Evans, Andria B aeva...@lghealth.org
 Subject: [Histonet] Biopsy program for Sakura VIP 5/6 Processor
 To: histonet@lists.utsouthwestern.edu
   histonet@lists.utsouthwestern.edu
 Message-ID:

 4182fdf23d7c9948bc41c4c082c3a54f021557b3a...@mail-ag-cluster.lha.org
 Content-Type: text/plain; charset=iso-8859-1

 Our lab is currently looking for a way to shorten our Biopsy 
 processing program without compromising the patient specimen.  We do 
 have an issue with our GI's being very dry, which causes us to have to 
 soak between each level taken and also causes a lot of chatter.  Also 
 we have a goal to do a run during the day to improve turn around time. 
 Here is what our current protocol is

 Formalin1 min   37degrees
 Formalin15 mins37degrees
 70 14 mins40 degrees
 95 14 mins40 degrees
 95 9 mins  40 degrees
 100   9 mins  40 degrees
 100   7 mins  40 degrees
 100   4 mins  40 degrees
 Xylene   23 minsno heat
 Xylene   15 minsno heat
 Paraffin  20 mins   60 degrees
 Paraffin  18 mins   60 degrees
 Paraffin  10 mins   60 degrees
 Paraffin  0 mins 60 degrees

 All the steps are set on a fast mix setting.  All of our biopsy 
 specimens are put into sponges.

 Any feedback would be greatly appreciated.

 Andria B Evans HTL(ASCP)CM
 Lancaster General Hospital
 555 North Duke Street
 Lancaster, PA  17604
 (717)544-5511 ext: 77329
 aeva...@lgheath.orgmailto:aeva...@lgheath.org

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Re: [Histonet] thermometer

2011-04-19 Thread Rene J Buesa
You can bay a certified digital thermometer for less than $35 and will be more 
than adequate for what you need.
René J.

--- On Mon, 4/18/11, Amber McKenzie amber.mcken...@gastrodocs.net wrote:


From: Amber McKenzie amber.mcken...@gastrodocs.net
Subject: [Histonet] thermometer
To: histonet@lists.utsouthwestern.edu
Date: Monday, April 18, 2011, 5:06 PM



My last CLIA inspection, I was told to check the temperature in the wax
chamber of my embedding station to compare against the temperature it
says it is...does anyone know of a good thermometer to purchase?



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Re: [Histonet] Tissue adhesion to slides

2011-04-19 Thread Rene J Buesa
Such thick sections are usually handled better if stained floating (not adhered 
to sledes).
René J.

--- On Tue, 4/19/11, Abbey Mortimer a.morti...@latrobe.edu.au wrote:


From: Abbey Mortimer a.morti...@latrobe.edu.au
Subject: [Histonet] Tissue adhesion to slides
To: Histonet@lists.utsouthwestern.edu Histonet@lists.utsouthwestern.edu
Date: Tuesday, April 19, 2011, 5:00 AM


Hello out there!

I was wondering if any of you have experience in attaching human retinae 
(~250-300 microns thick) to slides for manual immunohistochemistry. Starfrost 
does not seem adequate.

Any advice would be greatly appreciated!
Regards,
Abbey


Abbey Mortimer
PhD Candidate
School of Psychological Science
La Trobe University
Bundoora, Victoria, 3083
AUSTRALIA

Phone: (03) 9479 2470
Email: a.morti...@latrobe.edu.au

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[Histonet] in-situ hybridization

2011-04-19 Thread Bales, Candy A
This questions is for the labs that do in-situ hybridization for diagnostic 
purposes. Do you take slides for ISH from other labs and if so, please contact 
me via my email.

My next question is; one of my doc's is interested in us doing ISH herein our 
lab but I have been putting her off with the fact that we do not need this very 
often, it is very expensive to start up, etc.
But she is persistent. Any suggestions for starting up this procedure, 
including vendor preferences for supplies? I know next to nothing about ISH 
other than what I have read on-line.

Thank you in advance
Candy



Candy Bales, HT
Chief Histologist
The University  of Texas Dental Branch at Houston
Diagnostic Sciences-Oral Pathology
6516 M.D. Anderson Blvd. # 3.093
Houston, TX 77030
713.500.4411 office
713.500.4416 fax

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[Histonet] slide drying ovens

2011-04-19 Thread Bell, Mandy
I'm looking for recommendations for a new slide drying oven.  Something 
relatively small, with convection.  Any input would be appreciated.  Thanks !
 
Mandy M Bell , HTL (ASCP)
Histology Department
Community Hospital of the Monterey Peninsula
831.625.4791
 
 
P Please consider the environment before printing this e-mail 

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[Histonet] Disposing of gross only items

2011-04-19 Thread Stella Mireles
Hello Everyone,

Need some info on the disposal of gross only items.
These items include hardware, wires, gallstones and foreign objects.

We are running out of room for the storage of gross only specimens.
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Re: [Histonet] slide drying ovens

2011-04-19 Thread Akemi Allison
There are many so called convection ovens out there that are gravity  
convection.  Biocare has a great convection oven that has an internal  
fan, and can be set with several different programs. You can set it  
for IHC at the end of the day and it automatically stops and is ready  
for you in the AM when you come in.  It has a small footprint. It is  
not cheap, but well worth it.



Akemi Allison BS, HT (ASCP) HTL
Director
Phoenix Lab Consulting
Tele: 408.335.9994
E-Mail: akemiat3...@yahoo.com

On Apr 19, 2011, at 10:13 AM, Bell, Mandy wrote:

I'm looking for recommendations for a new slide drying oven.   
Something relatively small, with convection.  Any input would be  
appreciated.  Thanks !


Mandy M Bell , HTL (ASCP)
Histology Department
Community Hospital of the Monterey Peninsula
831.625.4791


P Please consider the environment before printing this e-mail

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[Histonet] Rabbit eye holder?

2011-04-19 Thread Laura Conner

Hi all,

I'm looking for something to hold my rabbit eyes in place (and other eyes if 
they're available like rat) while cutting them in half before further 
processing. My boss said he used them a long time ago but doesn't know what 
they're called. I can't figure out what they'd be called either but I'd like to 
buy some if they exist.

Any input? Ideas?

Thanks!

Laura

  
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[Histonet] 3, 000 Breast Cancer Specimens from Quebec Breast Cancer being retested

2011-04-19 Thread Akemi Allison
PhenoPath Laboratories Retests Nearly 3,000 Breast Cancer Specimens  
from Quebec Breast Cancer specimens which may have been misdiagnosed.  
In the re-analysis, results of which were just announced, a total of  
87 women were found to have received a false negative result from the  
original pathology laboratory tests in Quebec. Of this number, 39  
were required to alter their treatment and among them five women  
died. Minister of Health Yves Bolduc said it was impossible to  
determine whether the women died as a result of being improperly  
treated. Check out this link. http://www.ihc.co/a824362-seattle-based- 
phenopath-laboratories-retests-nearly-.cfm



Akemi Allison BS, HT (ASCP) HTL
Director
Phoenix Lab Consulting
Tele: 408.335.9994
E-Mail: akemiat3...@yahoo.com

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[Histonet] unsubscribe

2011-04-19 Thread Mahoney,Janice A



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Re: [Histonet] in-situ hybridization

2011-04-19 Thread Emily Sours
Roche Diagnostics has great DIG labels, antibodies and color reaction
chemicals.
It is a pain to just start up, you need to buy a lot of stuff for it.  Could
you use someone else's set up and pay for part of the chemicals?

Emily


A great book should leave you with many experiences, and slightly exhausted.
You should live several lives while reading it.
-William Styron



On Tue, Apr 19, 2011 at 12:51 PM, Bales, Candy A
candy.a.ba...@uth.tmc.eduwrote:

 This questions is for the labs that do in-situ hybridization for diagnostic
 purposes. Do you take slides for ISH from other labs and if so, please
 contact me via my email.

 My next question is; one of my doc's is interested in us doing ISH herein
 our lab but I have been putting her off with the fact that we do not need
 this very often, it is very expensive to start up, etc.
 But she is persistent. Any suggestions for starting up this procedure,
 including vendor preferences for supplies? I know next to nothing about ISH
 other than what I have read on-line.

 Thank you in advance
 Candy



 Candy Bales, HT
 Chief Histologist
 The University  of Texas Dental Branch at Houston
 Diagnostic Sciences-Oral Pathology
 6516 M.D. Anderson Blvd. # 3.093
 Houston, TX 77030
 713.500.4411 office
 713.500.4416 fax

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[Histonet] Re: Standardization??? 3, 000 Breast Cancer Specimens from Quebec Breast Cancer being retested

2011-04-19 Thread Akemi Allison
From what I have experienced in my observations of various labs;  
numerous labs do not follow proper standardization practices which  
are set by FDA guidelines for Her2-neu.  Prognostic markers are  
particularly susceptible to heat. Baking slides in excess  
temperatures (over 62 degrees C) for prolonged lengths of time can  
also drop the antigenicity of the test tissues a full grade.  There  
has been documentation of this through publications.  Temperatures  
MUST be monotored and recorded. The Antigen Retrieval Process is very  
important and QC measures MUST be followed. Internal temperature and  
pressure MUST be met and recorded.  QC monitor strips will record and  
show any irregularities in this step. If the pressure and temp has  
not been met, the test should be repeated. A lot of IHC techs do not  
monitor this process.  Unfortunately, internal laboratory  
standardization can vary from shift to shift.  Just think about non- 
standardization practices throughout the country because of under- 
education and strict adherence to established guidelines.



Akemi Allison BS, HT (ASCP) HTL
Director
Phoenix Lab Consulting
Tele: 408.335.9994
E-Mail: akemiat3...@yahoo.com

On Apr 19, 2011, at 10:36 AM, Akemi Allison wrote:

PhenoPath Laboratories Retests Nearly 3,000 Breast Cancer Specimens  
from Quebec Breast Cancer specimens which may have been  
misdiagnosed. In the re-analysis, results of which were just  
announced, a total of 87 women were found to have received a false  
negative result from the original pathology laboratory tests in  
Quebec. Of this number, 39 were required to alter their treatment  
and among them five women died. Minister of Health Yves Bolduc said  
it was impossible to determine whether the women died as a result  
of being improperly treated. Check out this link. http://www.ihc.co/ 
a824362-seattle-based-phenopath-laboratories-retests-nearly-.cfm



Akemi Allison BS, HT (ASCP) HTL
Director
Phoenix Lab Consulting
Tele: 408.335.9994
E-Mail: akemiat3...@yahoo.com

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[Histonet] Re: Histonet Biopsy Program for Sakura VIP 5/6 Processor

2011-04-19 Thread Johnson, Teri
Wow, somehow I missed this email. Sorry for the delay.

Andria, take the heat off your alcohols. Keep it on the formalin and the 
paraffin, but do the rest of the processing at ambient temperature. Make sure 
you put only small soft tissues on this schedule though, tougher collagenous 
skin specimens might not process well enough with the quick dehydration times 
you have.

I am curious how you arrived at the timing for the steps. 14 minutes, 9 
minutes, 7 minutes, 23 minutes, etc?

Good luck and best wishes,

Teri

Teri Johnson, HT(ASCP)QIHC
Head, Histology and Electron Microscopy
Stowers Institute for Medical Research
Kansas City, MO


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[Histonet] IHC validation

2011-04-19 Thread Ring, Mary L
Does a change in the type of hematoxylin counterstain require any re-validation 
of IHC stains?
Thanks for your help!

Mary Ring, HT, QIHC
Regions Hospital, St Paul, Mn


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[Histonet] Tissue Microarray

2011-04-19 Thread Kiranjit Grewal

Are you using tissue microarrays as controls for all your routine IHC stains 
(not antibody validation or research) ? If so, how are you making the arrays?
 
thank you,
 
-Kiranjit
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Re: [Histonet] Disposing of gross only items

2011-04-19 Thread Rene J Buesa
First talk to your legal department, just in case!
René J.

--- On Tue, 4/19/11, Stella Mireles estellamire...@gmail.com wrote:


From: Stella Mireles estellamire...@gmail.com
Subject: [Histonet] Disposing of gross only items
To: Histonet@lists.utsouthwestern.edu
Date: Tuesday, April 19, 2011, 1:22 PM


Hello Everyone,

Need some info on the disposal of gross only items.
These items include hardware, wires, gallstones and foreign objects.

We are running out of room for the storage of gross only specimens.
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Re: [Histonet] IHC validation

2011-04-19 Thread Rene J Buesa
Not really because the Hematoxylin should affect only the nuclei UNLESS it is 
a nuclear antibody, in which case the antigenic reaction could be obscured. 
For nuclear Abs I used to dilute my hematoxylin as much as possible or did not 
use it at all.
René J.

--- On Tue, 4/19/11, Ring, Mary L mary.l.r...@healthpartners.com wrote:


From: Ring, Mary L mary.l.r...@healthpartners.com
Subject: [Histonet] IHC validation
To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
Date: Tuesday, April 19, 2011, 3:04 PM


Does a change in the type of hematoxylin counterstain require any re-validation 
of IHC stains?
Thanks for your help!

Mary Ring, HT, QIHC
Regions Hospital, St Paul, Mn


This e-mail and any files transmitted with it are confidential and are intended 
solely for the use of the individual or entity to whom they are addressed. If 
you are not the intended recipient or the individual responsible for delivering 
the e-mail to the intended recipient, please be advised that you have received 
this e-mail in error and that any use, dissemination, forwarding, printing, or 
copying of this e-mail is strictly prohibited.

If you have received this e-mail in error, please immediately notify the 
HealthPartners Support Center by telephone at (952) 967-6600. You will be 
reimbursed for reasonable costs incurred in notifying us. HealthPartners R001.0
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Re: [Histonet] IHC validation

2011-04-19 Thread Richard Cartun
In my opinion, only if it affects immunoreactivity.

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


 Ring, Mary L mary.l.r...@healthpartners.com 4/19/2011 3:04 PM 
Does a change in the type of hematoxylin counterstain require any re-validation 
of IHC stains?
Thanks for your help!

Mary Ring, HT, QIHC
Regions Hospital, St Paul, Mn


This e-mail and any files transmitted with it are confidential and are intended 
solely for the use of the individual or entity to whom they are addressed. If 
you are not the intended recipient or the individual responsible for delivering 
the e-mail to the intended recipient, please be advised that you have received 
this e-mail in error and that any use, dissemination, forwarding, printing, or 
copying of this e-mail is strictly prohibited.

If you have received this e-mail in error, please immediately notify the 
HealthPartners Support Center by telephone at (952) 967-6600. You will be 
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[Histonet] AUTO: Carolyn J Kent is out of the office. (returning 04/21/2011)

2011-04-19 Thread CKent

I am out of the office until 04/21/2011.

I will respond to your message when I return.


Note: This is an automated response to your message  Histonet Digest, Vol
89, Issue 21 sent on 4/19/2011 12:02:59 PM.

This is the only notification you will receive while this person is away.


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[Histonet] whole retinal staining

2011-04-19 Thread David A. Wright
Dear Abbey  Histonet

I agree with René Buesa: I would try to stain whole retinae by a 'floating 
section' method i.e. hand processing in a dipping tray or mesh baskets (brush 
transfer can be done too but is laborious). Then mount them at the end.

Floating allows reagents to penetrate from both sides of the retina - extra 
valuable because your incubation times are going to be very long with material 
this thick. (I assume you are not just interested in superficial layers.) A 
microwave processor would help with penetration, but I have no direct 
experience. 

-David
==
David A. Wright, Ph.D.
University of Chicago
Section of Neurosurgery

ORIGINAL POST:
Histonet Digest, Vol 89, Issue 21 Message: 7
Date: Tue, 19 Apr 2011 19:00:27 +1000
From: Abbey Mortimer a.morti...@latrobe.edu.au
Subject: [Histonet] Tissue adhesion to slides


Hello out there!

I was wondering if any of you have experience in attaching human retinae 
(~250-300 microns thick) to slides for manual immunohistochemistry. Starfrost 
does not seem adequate.

Any advice would be greatly appreciated!
Regards,
Abbey


Abbey Mortimer
PhD Candidate
School of Psychological Science
La Trobe University
Bundoora, Victoria, 3083
AUSTRALIA

Phone: (03) 9479 2470
Email: a.morti...@latrobe.edu.au 

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[Histonet] RE: IHC on frozen sections

2011-04-19 Thread Tony Henwood
Jana,

Since you are fixing in formaldehyde, why not paraffin embed them?
Frozen sectioning of formalin fixed tissue and doing IPX on them is difficult 
as well as problems with storing the tissue.
I would cut frozen of unfixed tissue and do IPX on them rather than doing IPX 
on formalin fixed frozen sections.

Any reason why you have chosen the frozen section of formalin fixed tissue?

Regards 
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA) 
Laboratory Manager  Senior Scientist 
Tel: 612 9845 3306 
Fax: 612 9845 3318 
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jane C. Moose
Sent: Wednesday, 20 April 2011 12:19 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] IHC on frozen sections

Following is question on behalf of   Jana Moose Ritter, DVM
janamo...@yahoo.com

 

 

We are going to perform IHC on frozen sections, and the tissues  (pig
aorta)  will be harvested on a Friday.

 

Histo lab is wondering:

 

1) can tissue fix in paraformaldehyde over the weekend until next steps 
(sucrose and frozen embedding to be completed on Monday) 

2) can fixative be switched to sucrose at the end of Friday (tissue would 
remain in sucrose until frozen embedding on Monday)

3) must complete the solution switch and entire frozen embedding process on 
Saturday

 

 

Thanks for your help. 

 

Jane Moose

LIS Coordinator

Newberry County Memorial Hospital

Newberry, SC  29108

P-803-405-7129

F- 803-405-7474

 

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