[Histonet] rat's hind paw skin

2013-12-02 Thread Leila Etemadi
Hello every body,

First I would like to thank you all for your great feedbacks and attention 
which is such a big improvement in my work, Thank you all!

Then, I was wonder if any one has experience on this tissue: rat hind paw skin 
( which is hairless).

Any inputs will be appreciated, whether is about any specific source where I 
can find technical information about fixation procedure..., or about 
sectioning,staining procedure…

 I am looking for melanin pigments and have no clue if it is possible to see it 
there or not?!?

Thanks in advance,

Cheers

Leila




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[Histonet] Labeling Error Policies

2013-12-02 Thread Beth.Fye
Our laboratories are currently working on policies to address specimen 
identification/labeling errors.  This is to be a laboratory policy and will 
include pathology.  Would anyone be willing to share policies that they have 
that address this and any punitive action that is mentioned?  I know this has 
been discussed before, and continues to be a hot topic.

Thanks in advance for your help regarding this.

Beth A. Fye, CT (ASCP)
Pathology Technical Manager
HCA Richmond Hospital Laboratories
office:  (804) 228-6564
fax:  (877)699-3895
mailto:beth@hcahealthcare.com

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RE: [Histonet] Rate of microtome injuries in Histotechnology schools.

2013-12-02 Thread Anne Murvosh
If anyone wants to cut down on cutting injuries.  Teach the new techs to
use two forceps instead of your fingers.  I'm too old to change but I
know a tech who cuts this way and has never had an injury.  It works
really well on automated microtomes.  Anne

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tom
Wells
Sent: Wednesday, November 27, 2013 12:11 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Rate of microtome injuries in Histotechnology
schools.

Hi,
I am curious about the rate of microtome cuts that students receive in
Histotechnology schools. We have a rather large program and take in
approximately 60 (or more)  students a year. Our Histotechnology
semester is around 20 weeks long. During that time our students cut
approximately 300 - 400 blocks per student. We typically have
approximately 10 minor cuts per semester. How does this compare to other
schools? Please email or call me directly to discuss this further. Thank
you very much. Tom

Tom Wells BSc, MEd, MLT, ART
Faculty
Department of Medical Laboratory Sciences, School of Health British
Columbia Institute of Technology SW03-3088, 3700 Willingdon Avenue
Burnaby, BC, V5G 3H2

E tom_we...@bcit.ca
T (604) 412-7594
C (778) 228 -4102 

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[Histonet] Embedding cells in Paraffin

2013-12-02 Thread Mike Tighe
Has anyone tried to embed cells grown in tissue culture? I am trying to put 
some tissue culture cells through same stress as tissue would go through. 
Fixation, dehydration, and heat. Any ideas? I could re-suspend in OCT and then 
fix for extended time with NBF but that doesn't quite seem fair.



Thanks for any ideas!
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[Histonet] embedding cells in parrafin #2

2013-12-02 Thread Helen Fedor
Making cell tissue blocks

Cells: 
.   Harvest and fix in formalin* for at least 3hrs or overnight (10 fold 
more formalin)
.   HAVE A NICE VISIBLE SIZE PELLET (1 confluent T75 minimum or 1 T175)
.   Remove formalin* and wash 2x's in cold 1x PBS
.   Cover cells with some 1x PBS and refrigerate

Materials for blocks:
1.  Toothpick or 20ul pipette tip
2.  Agarose  (2% solution agarose with 1xPBS)
ultra pure agarose cat#15510-027 from core

3.  Cells in 1x PBS
4.  0.5ml microtubes (sterile)
5.  Tissue cassettes (1 or 6 compartiment cassettes -Electron Microscopy
 Science 800-523-5874 cat.# 70078-W)  
6.  New razor blades
7.  Clean cutting board
8.  Container to submerge cassette into with enough 1x PBS to cover 
cassettes

Method:
.   Suspend cells in 1xPBS - use just enough to pipette cells (1:1 dilution 
is MAX)
.   Make 2% agarose solution - keep in water bath (42C) so doesn't solidify
.   Make 200ul agarose plug in 0.5ml tube and wait 3 minutes to solidify 
.   Add *120ul of cell solution to .5ml tube and then add *150ul of agarose 
and pipette up/down ~3 times to mixed well - CUT END OF PIPETTE TIP OFF JUST A 
LITTLE SO YOU DON'T DESTROY CELL IF NECESSARY
.   Add toothpick and let sit 5 minutes
.   Remove plug with toothpick and cut into sections (if necessary) with 
new blade on clean surface and add to cassette
.   If you have extra cell plugs then store then in 1x PBS in frig.

* Varies according to how much cell suspension you have. ALWAYS add at least 
30ul more of agarose in order for it to make a nice plug.

IMPORTANT NOTES:
.   ALWAYS be sure to label your cassette with an experiment number because 
that's what the slides will be labeled with.
.   Be SURE to write on BOTH the top of the cassette and down the sides 
what cell type is in each compartment (if using a 6 compartment cassette)
.   Tell the histologist what you fixed your cells in - if fixed in 
formalin, ethanol, paraformaldehyde, etc. - this is vital for the 
processing/embedding process
.   ALWAYS put control cell types in the block  - +/-
.   ALWAYS prepare your block in an asymmetric pattern THIS IS A MUST!! or 
you will not be able to identify which cell type is placed where on the slide
Helen L. Fedor 

Prostate Tissue Bank, Manager
Oncology Tissue Services, Manager
Johns Hopkins University
600 N. Wolfe St, | Marburg Room 406
Baltimore, MD | 21287-7065

410.614.1660

http://tmalab.jhmi.edu/
http://prostatebiorepository.org/



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike Tighe
Sent: Monday, December 02, 2013 12:06 PM
To: histonet@lists.utsouthwestern.edu (histonet@lists.utsouthwestern.edu)
Subject: [Histonet] Embedding cells in Paraffin

Has anyone tried to embed cells grown in tissue culture? I am trying to put 
some tissue culture cells through same stress as tissue would go through. 
Fixation, dehydration, and heat. Any ideas? I could re-suspend in OCT and then 
fix for extended time with NBF but that doesn't quite seem fair.



Thanks for any ideas!
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[Histonet] Purple/Blue haze on ISH

2013-12-02 Thread Bauer, Karen L.
Hi all... sending out for a colleague...

After implementing the Vantage system, a lot of their ISH slides have a 
purplish to bluish haze on the slides.  Not all of them, but some and it seems 
to be consistent.  No problems before Vantage.  They were using the longer 
labels from Ventana for labeling prior to implementation, but now with Vantage, 
the slide labels are smaller.  That's the only real difference from before and 
after.  Protocols have not changed and they've checked everything else... 
buffers and such.

Any ideas on why this would happen?

Thank you,

Karen

Karen L. Bauer HTL/HT (ASCP) | Histology Supervisor | Pathology | MOHS Lab 
Supervisor | Dermatology | Phone: 715-838-3205 | 
bauer.ka...@mayo.edumailto:bauer.ka...@mayo.edu | Mayo Clinic Health System | 
1221 Whipple Street | Eau Claire, WI 54702 | 
mayoclinichealthsystem.orghttp://www.mayoclinichealthsystem.org/


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[Histonet] RE: Purple/Blue haze on ISH

2013-12-02 Thread Obregon, Cecilia
Karen,

We experienced a similar problem with the ISHs at our laboratory a few months 
ago with the Kappa, Lambda, Eber and HPV. Our pathologists were complaining of 
a blue crystal-like precipitate on all ISH slides.  

Our Ventana Technical Specialist recommended that we try the NO ALCOHOL 
dehydrating procedure. (The same one we currently use for the Red-Alkaline 
Phosphatase detection). Once you remove the slides from the Ultra or XT rinse 
throughly in soapy water and put in the 60 Degrees oven for 15 minutes. 
Dehydrate in the Symphony using a NO DEHYDRATION coverslip program. 

We have noticed a signficant decrease in this precipitate using this procedure. 
Hope if works for you too. 

Thank you,

Cecilia M. Obregon
Memorial Regional Hospital 
3501 Johnson Street
Hollywood, FL 33021
Ph: 954-265-5317


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Bauer, Karen L. 
[bauer.ka...@mayo.edu]
Sent: Monday, December 02, 2013 12:08 PM
To: 'histonet'
Subject: [Histonet] Purple/Blue haze on ISH

Hi all... sending out for a colleague...

After implementing the Vantage system, a lot of their ISH slides have a 
purplish to bluish haze on the slides.  Not all of them, but some and it seems 
to be consistent.  No problems before Vantage.  They were using the longer 
labels from Ventana for labeling prior to implementation, but now with Vantage, 
the slide labels are smaller.  That's the only real difference from before and 
after.  Protocols have not changed and they've checked everything else... 
buffers and such.

Any ideas on why this would happen?

Thank you,

Karen

Karen L. Bauer HTL/HT (ASCP) | Histology Supervisor | Pathology | MOHS Lab 
Supervisor | Dermatology | Phone: 715-838-3205 | 
bauer.ka...@mayo.edumailto:bauer.ka...@mayo.edu | Mayo Clinic Health System | 
1221 Whipple Street | Eau Claire, WI 54702 | 
mayoclinichealthsystem.orghttp://www.mayoclinichealthsystem.org/


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RE: [Histonet] Embedding cells in Paraffin

2013-12-02 Thread joelle weaver
I spun down the cultured cells and then used a product called histogel. It kept 
them protected through the VIP, paraffin embedded like cell block buttons and 
was able to cut regular paraffin sections. I believe that I purchased the 
histogel from American Mastertech. 




Joelle Weaver MAOM, HTL (ASCP) QIHC
 
 From: mti...@trudeauinstitute.org
 To: histonet@lists.utsouthwestern.edu
 Date: Mon, 2 Dec 2013 17:06:24 +
 Subject: [Histonet] Embedding cells in Paraffin
 
 Has anyone tried to embed cells grown in tissue culture? I am trying to put 
 some tissue culture cells through same stress as tissue would go through. 
 Fixation, dehydration, and heat. Any ideas? I could re-suspend in OCT and 
 then fix for extended time with NBF but that doesn't quite seem fair.
 
 
 
 Thanks for any ideas!
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[Histonet] RE: Embedding cells in Paraffin

2013-12-02 Thread Morken, Timothy
Mike,

For EM work we fix, scrape the plate into a microtube, centrifuge at 1800  rpm 
for 10 min and then embed in Histogel or agar. Processing after that is as 
usual. They look fine by EM. I'm sure they would look fine by paraffin 
processing as well.

Tim Morken
Supervisor, Electron Microscopy and Neuromuscular Special Studies
UC San Francisco Medical Center
San Francisco, CA


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike Tighe
Sent: Monday, December 02, 2013 9:06 AM
To: histonet@lists.utsouthwestern.edu (histonet@lists.utsouthwestern.edu)
Subject: [Histonet] Embedding cells in Paraffin

Has anyone tried to embed cells grown in tissue culture? I am trying to put 
some tissue culture cells through same stress as tissue would go through. 
Fixation, dehydration, and heat. Any ideas? I could re-suspend in OCT and then 
fix for extended time with NBF but that doesn't quite seem fair.



Thanks for any ideas!
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[Histonet] Donations Needed

2013-12-02 Thread Stritmatter, Andrea N
Dear Histo Folks,

I am in the process of setting up a brand new histology/IHC laboratory on the 
campus of the Uganda Cancer Institute in Kampala, Uganda in conjunction with 
the Fred Hutchinson Cancer Research Center.  As you can imagine, we need 
anything and everything as supplies and small equipment are extremely hard to 
obtain in Uganda.  If anyone is doing any end-of-year cleaning and would like 
to donate to a very worthy endeavor, please let me know.  We are in need of 
everything from paraffin pots to weigh boats, beakers to vortex machines, dyes 
to amber bottles, and forceps to staining jars.

Please don't hesitate to contact me with any questions.

Thanks so much!

Andrea

Andrea Stritmatter, HTL (ASCP)
QA Manager
UCI/Hutchinson Center Cancer Alliance

Fred Hutchinson Cancer Research Center
1100 Fairview Ave N, M1-B140
Seattle, WA 98109-1024

Office phone: +1-206-667-2913
Cell phone: +1-206-495-7081
Fax: +1-206-667-1965
Skype address: andrea.stritmatter
Email:  astri...@fhcrc.org

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[Histonet] anti-Human CD20

2013-12-02 Thread Mike Tighe
Thanks for all the great replies!! While I have you all worried about my cell 
pellets ;-) Does anyone have a good anti-HuCD20 that works well for FFPE 
tissues (cells).



Thanks!

Mike
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[Histonet] RE: See you Soon

2013-12-02 Thread Mayer,Toysha N
Congratulations Sarah 

Sincerely,

Toysha N. Mayer, MBA, HT(ASCP)
tnma...@mdanderson.org
Instructor/Education Coordinator
Program in Histotechnology
School of Health Professions
MD Anderson Cancer Center
713-563.3481



Message: 1
Date: Wed, 27 Nov 2013 19:13:05 +
From: Sarah Dysart sdys...@mirnarx.com
Subject: [Histonet] See You Soon
To: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:

488dd7f2012c47899d4a47bfba5c9...@by2pr07mb106.namprd07.prod.outlook.com

Content-Type: text/plain; charset=us-ascii

Hey guys and gals...I have taken a new position as Pathology Supervisor at 
North Austin Medical Center here in Austin...so I am unsubscribing for now, but 
have no fear...I will be back ASAP with my new email address.  Hope everyone 
has a great Turkey Day!!

Signing off for now...

Sarah Goebel-Dysart, BA, HT(ASCP), QIHC (ASCP) Histotechnologist Mirna 
Therapeutics
2150 Woodward Street
Suite 100
Austin, Texas  78744
(512)901-0900 ext. 6912



--

Message: 2
Date: Wed, 27 Nov 2013 11:32:22 -0800
From: Heather Marlatt hmarlat...@gmail.com
Subject: Re: [Histonet] See You Soon
To: Sarah Dysart sdys...@mirnarx.com
Cc: histonet@lists.utsouthwestern.edu
histonet@lists.utsouthwestern.edu
Message-ID:
calavvk6ywzb8kqxt4s+veodxcdftpwzo4vdldaq1zxp8nmp...@mail.gmail.com
Content-Type: text/plain; charset=ISO-8859-1

CONGRATULATIONS SARAH! I hope you love the new position!

:-)


On Wed, Nov 27, 2013 at 11:13 AM, Sarah Dysart sdys...@mirnarx.com wrote:

 Hey guys and gals...I have taken a new position as Pathology 
 Supervisor at North Austin Medical Center here in Austin...so I am 
 unsubscribing for now, but have no fear...I will be back ASAP with my 
 new email address.  Hope everyone has a great Turkey Day!!

 Signing off for now...

 Sarah Goebel-Dysart, BA, HT(ASCP), QIHC (ASCP) Histotechnologist Mirna 
 Therapeutics
 2150 Woodward Street
 Suite 100
 Austin, Texas  78744
 (512)901-0900 ext. 6912

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[Histonet] Grossing tables

2013-12-02 Thread Amber McKenzie
I'm currently designing a new GI lab.  Any advice on grossing stations?  The 
only name I know is Mopec.  Is that the best one to go with or are there better 
ones out there? Thanks!


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[Histonet] RE: Grossing tables

2013-12-02 Thread Weems, Joyce K.
I think that's the best - you can charge for rides - up and down!!

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 Amber McKenzie
Sent: Monday, December 02, 2013 4:20 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Grossing tables

I'm currently designing a new GI lab.  Any advice on grossing stations?  The 
only name I know is Mopec.  Is that the best one to go with or are there better 
ones out there? Thanks!


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RE: [Histonet] RE: Grossing tables

2013-12-02 Thread Douglas Porter
http://www.thermoscientific.com/en/products/pathology-work-stations.html


Douglas A. Porter, HT (ASCP) 
Grossing Technician 
IT Coordinator
Cancer Registrar 

CAP-Lab, PLC 
2508 South Cedar Street 
Lansing, MI 48910-3138 

517-372-5520 (phone) 
517-372-5540 (fax) 

doug.por...@caplab.org 

www.caplab.org  
 
 
The information contained in this message may be privileged and/or
confidential and protected from disclosure. If the reader of this message is
not the intended recipient, you are hereby notified that any dissemination,
distribution, copying, forwarding or capture of this communication is
strictly prohibited. If you have received this communication in error,
please notify me immediately by return e-mail and delete this and all
copies. Thank-you.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, Joyce
K.
Sent: Monday, December 02, 2013 4:24 PM
To: 'Amber McKenzie'; 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] RE: Grossing tables

I think that's the best - you can charge for rides - up and down!!

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 Amber
McKenzie
Sent: Monday, December 02, 2013 4:20 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Grossing tables

I'm currently designing a new GI lab.  Any advice on grossing stations?  The
only name I know is Mopec.  Is that the best one to go with or are there
better ones out there? Thanks!


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[Histonet] Re: [IHCRG] macrophage eq markers?

2013-12-02 Thread Mehmet Fatih BOZKURT
In which animals works also this antibody ?

Thanks


On Mon, Dec 2, 2013 at 11:20 PM, Jan Shivers shive...@umn.edu wrote:

 Dako's MAC 387 (cat. #: M0747)


 On Mon, Dec 2, 2013 at 2:09 PM, Jackie Ferracone 
 ferra...@vet.upenn.eduwrote:

  Hi All,

 Looking for good macrophage markers for equine tissue, FFPE IHC .?

 Thanks















 Jackie Ferracone,  B.Sc.

 Research Specialist

 Dept. of Pathobiology

 University of Pennsylvania

 School of Veterinary Medicine

 382 West Street Road

 Kennett Square, PA 19348-1692

 610-925-6391

 610-350-8860 (cell)

 610-925-6810  (fax)



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 To contact the National Society for Histotechnology, email: histo@nsh.orgor 
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 --
 Jan Shivers
 Senior Scientist
 IHC/Histology Section Head
 Pathology Teaching Program
 Veterinary Diagnostic Laboratory
 University of Minnesota
 1333 Gortner Ave.
 St. Paul, MN  55108
 612-624-7297
 shive...@umn.edu

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

2013-12-02 Thread Lee Peggy Wenk
Sad news. I received an email over the weekend from a histotech, that Chris van 
der Loos died on Nov. 26, 2013. I was able to talk with the NSH office today, 
and got it confirmed. There is information about Chris on the NSH webpage as of 
later this morning.
http://www.nsh.org/content/remembering-dr-chris-van-der-loos-august-2-1955-%E2%80%93-november-26-2013

Peggy A. Wenk. HTL(ASCP)SLS
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[Histonet] Re: [IHCRG] macrophage eq markers?

2013-12-02 Thread Jan Shivers
I've had it to work in cat, cow, dog, fox, horse, otter, pig, and raccoon
in my lab.

According to vendor - it's supposed to also work in guinea pig, monkey,
rabbit, and rat, but I have not tried it in those animals

Needs either enzyme digestion or heat antigen retrieval.


Best regards,
Jan Shivers


On Mon, Dec 2, 2013 at 3:37 PM, Mehmet Fatih BOZKURT fbozk...@gmail.comwrote:

 In which animals works also this antibody ?

 Thanks


 On Mon, Dec 2, 2013 at 11:20 PM, Jan Shivers shive...@umn.edu wrote:

 Dako's MAC 387 (cat. #: M0747)


 On Mon, Dec 2, 2013 at 2:09 PM, Jackie Ferracone 
 ferra...@vet.upenn.eduwrote:

  Hi All,

 Looking for good macrophage markers for equine tissue, FFPE IHC .?

 Thanks















 Jackie Ferracone,  B.Sc.

 Research Specialist

 Dept. of Pathobiology

 University of Pennsylvania

 School of Veterinary Medicine

 382 West Street Road

 Kennett Square, PA 19348-1692

 610-925-6391

 610-350-8860 (cell)

 610-925-6810  (fax)



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 --
 Jan Shivers
 Senior Scientist
 IHC/Histology Section Head
 Pathology Teaching Program
 Veterinary Diagnostic Laboratory
 University of Minnesota
 1333 Gortner Ave.
 St. Paul, MN  55108
 612-624-7297
 shive...@umn.edu

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 You received this message because you are subscribed to the Google
 Groups ihcrg group. The IHC Resource Group is a standing committee
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 call
 443.535.4060.

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




-- 
Jan Shivers
Senior Scientist
IHC/Histology Section Head
Pathology Teaching Program
Veterinary Diagnostic Laboratory
University of Minnesota
1333 Gortner Ave.
St. Paul, MN  55108
612-624-7297
shive...@umn.edu
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RE: [Histonet] Chris van der Loos

2013-12-02 Thread Bea DeBrosse-Serra
Very sad news indeed. He will be missed dearly!

Beatrice DeBrosse-Serra HT(ASCP)QIHC
Isis Pharmaceuticals
Antisense Drug Discovery
2855 Gazelle Ct.
Carlsbad, CA 92010
760-603-2371



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lee  Peggy Wenk
Sent: Monday, December 02, 2013 1:46 PM
To: Histonet
Subject: [Histonet] Chris van der Loos

Sad news. I received an email over the weekend from a histotech, that Chris van 
der Loos died on Nov. 26, 2013. I was able to talk with the NSH office today, 
and got it confirmed. There is information about Chris on the NSH webpage as of 
later this morning.
http://www.nsh.org/content/remembering-dr-chris-van-der-loos-august-2-1955-%E2%80%93-november-26-2013

Peggy A. Wenk. HTL(ASCP)SLS
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RE: [Histonet] Chris van der Loos

2013-12-02 Thread Tony Henwood (SCHN)
This is very sad.

Chris was knowledgeable, with a wonderful sense of humour and always had time 
for his colleagues.

He will be missed

Regards 
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA) 
Laboratory Manager  Senior Scientist, the Children's Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney 

Tel: 612 9845 3306 
Fax: 612 9845 3318 
Pathology Department
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 Lee  Peggy Wenk
Sent: Tuesday, 3 December 2013 8:46 AM
To: Histonet
Subject: [Histonet] Chris van der Loos

Sad news. I received an email over the weekend from a histotech, that Chris van 
der Loos died on Nov. 26, 2013. I was able to talk with the NSH office today, 
and got it confirmed. There is information about Chris on the NSH webpage as of 
later this morning.
http://www.nsh.org/content/remembering-dr-chris-van-der-loos-august-2-1955-%E2%80%93-november-26-2013

Peggy A. Wenk. HTL(ASCP)SLS
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[Histonet] Chris van der Loos

2013-12-02 Thread Manavis, Jim (Health)
I had the privilege and good fortune of getting to know and swap ideas with 
Chris after spending a few weeks with him in Breda back in 2001.

Never short of advice and always willing to help and learn from others.

To use an Australian expression he was an absolute Cracker of a guy.

Cheers

Jim


Jim Manavis

Laboratory Manager

Hanson Institute

Centre for Neurological Diseases

SA Pathology, Adelaide, SA, 5000

Australia

Phone: 61-08-8222-3668 / 0401120697

FAX: 61-08-8222 3392

email: jim.mana...@imvs.sa.gov.au

Disclaimer: Not this little black duck!

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[Histonet] RE: Chris van der Loos

2013-12-02 Thread Tony Henwood (SCHN)
I agree

Regards 
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA) 
Laboratory Manager  Senior Scientist, the Children's Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney 

Tel: 612 9845 3306 
Fax: 612 9845 3318 
Pathology Department
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 Manavis, Jim 
(Health)
Sent: Tuesday, 3 December 2013 10:37 AM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Chris van der Loos

I had the privilege and good fortune of getting to know and swap ideas with 
Chris after spending a few weeks with him in Breda back in 2001.

Never short of advice and always willing to help and learn from others.

To use an Australian expression he was an absolute Cracker of a guy.

Cheers

Jim


Jim Manavis

Laboratory Manager

Hanson Institute

Centre for Neurological Diseases

SA Pathology, Adelaide, SA, 5000

Australia

Phone: 61-08-8222-3668 / 0401120697

FAX: 61-08-8222 3392

email: jim.mana...@imvs.sa.gov.au

Disclaimer: Not this little black duck!

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sender, and are not necessarily the views of The Sydney Children's Hospitals 
Network.

This note also confirms that this email message has been virus scanned and 
although no computer viruses were detected, The Sydney Childrens Hospital's 
Network accepts no liability for any consequential damage resulting from email 
containing computer viruses.
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Re: [Histonet] rat's hind paw skin

2013-12-02 Thread Barry Rittman
Hi Leila
As no one seems to have responded to your email I will add a few items.
I used to do some work on wound healing on mouse footpads so circumstances
are the same.
If you are looking for melanin routine fixation and processing should be
finem, melanin will remain.
Only thing is that the epidermis is tough and there is not much dermis in
this region.
Need to make sure that you are careful in cutting sections or the epidermis
will separate.
Hope this helps
if you need any more details please email me.
Barry



On Mon, Dec 2, 2013 at 3:44 AM, Leila Etemadi leila.etem...@med.lu.sewrote:

 Hello every body,

 First I would like to thank you all for your great feedbacks and attention
 which is such a big improvement in my work, Thank you all!

 Then, I was wonder if any one has experience on this tissue: rat hind paw
 skin ( which is hairless).

 Any inputs will be appreciated, whether is about any specific source where
 I can find technical information about fixation procedure..., or about
 sectioning,staining procedure…

  I am looking for melanin pigments and have no clue if it is possible to
 see it there or not?!?

 Thanks in advance,

 Cheers

 Leila




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[Histonet] (no subject)

2013-12-02 Thread Amos Brooks
Hi,
There are a few ways of doing this. Perhaps the easiest  is scraping the 
cells off while it is still in the media. Transfer it to a centrifuge tube and 
spin it down. Pour off the supernatant add formalism vortex it and centrifuge 
it again and pour off the supernatant again and add Histogel or agar. Then 
process as usual. This is about as close as you are going to get to treating it 
like normal tissue.

Amos


Message: 4 Date: Mon, 2 Dec 2013 17:06:24 + From: Mike Tighe 
mti...@trudeauinstitute.org Subject: [Histonet] Embedding cells in Paraffin 
To: histonet@lists.utsouthwestern.edu (histonet@lists.utsouthwestern.edu) 
histonet@lists.utsouthwestern.edu Message-ID: 
46d5589df0864870848089e6780fb...@by2pr07mb469.namprd07.prod.outlook.com

Content-Type: text/plain; charset=us-ascii

Has anyone tried to embed cells grown in tissue culture? I am trying to put 
some tissue culture cells through same stress as tissue would go through. 
Fixation, dehydration, and heat. Any ideas? I could re-suspend in OCT and then 
fix for extended time with NBF but that doesn't quite seem fair.

Thanks for any ideas!___
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