[Histonet] NSH Meeting Hotels

2009-08-13 Thread Akemi Allison-Tacha
Hi All,
Anyone trying to reserve a room at the Doubletree should read this.
I just tried to reserve a room for the upcoming Symposium.  I went to the NSH 
website and looked under the "Hotel & Travel" icon and saw that the only hotel 
that wasn't Sold Out was the Double Tree.  I called and they never heard of us 
"NSH". I read all the information to the reservation person and she came up 
with a blank.  I requested the supervisor.  After searching for about 15 
minutes, she found us under histotechnology.  Anyone trying to book a room 
should state that our GROUP CODE is "CI0N" 

Akemi Allison-Tacha BS, HT(ASCP)HTL
Histology Manager
APMG Laboratories
105A Cooper Court, Los Gatos, CA 95032
Contact: 800.848.2764
V/M: 408.884.2718
Fax: 408.884.2758
Cell: 408.335.9994
(W) E-Mail: aallison-ta...@apmglab.com
(P) E-Mail: akemiat3...@yahoo.com

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Negative Staining Positive

2009-08-13 Thread Histonet Alias
Has anyone noticed their negative mouse having some positive staining using
the Ventana Benchmark XT? We use the iview detection. Any ideas? Thank you.

-- 
Al Ias HT(ASCP)
Histology Manager
Pathology Laboratory
United States
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] job opportunity for technologist interested in development of educational materials

2009-08-13 Thread Barbara Cebulski
This is a great opportunity for someone with expertise in laboratory
medicine and in education.

MediaLabInc. (http://www.medialabinc.net), located in metro Atlanta, GA, is
a leading provider of online compliance and training software for the
clinical laboratory industry. We presently deliver over 300,000 online
course events to individuals and institutions annually, and our customer
base continues to expand, as does the depth, breath, and quality of our
course offerings.

We are seeking an additional medical technologist (MT) to join our team.
Experience as a classroom or online educator and experience in writing
technical or educational materials is essential. Sub-speciality training,
experience in laboratory administration, safety, or compliance would be
helpful. Knowledge or experience in instructional design, digital
photography, photomicroscopy, and video production will also be considered.
We realize that no one individual will have all these skills, but a strong
background as a clinical laboratorian and educator is essential, and all
interested MT applicants with at least 5 years of laboratory and/or
educational experience are strongly encouraged to apply.

The successful candidate will work closely with our team to help us to
develop and update courseware that continues to meet the ever changing needs
of clinical laboratories. He or she will also work with other contributing
course authors and local laboratory managers and technologists.

Pay and benefits are negotiable and highly competitive. Work from home
several days per week, and enjoy working in our comfortable office in
suburban Atlanta the rest of the time. Some opportunity for travel is
available. Preference will be given to residents of metro Atlanta, but we
will consider an outstanding candidate from the United States or Canada who
is willing to relocate. We will also consider part-time employment for the
right candidate who wants to work from his / her home location in the U.S.
or Canada.

Please send your CV to Paul Fekete, MD, via email attachment to
fek...@gmail.com.

For more information about MediaLab, visit http://www.medialabinc.net.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Laura Miller is on vacation.

2009-08-13 Thread Laura . Miller

I will be out of the office starting  08/13/2009 and will not return until
08/17/2009.

I will respond to your email on Monday.  Thanks!


__
This email has been scanned by the MessageLabs Email Security System.
For more information please visit http://www.messagelabs.com/email 
__

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: [Histonet] Specimen Storage

2009-08-13 Thread Rene J Buesa
We used to store them directly in the sealed Kapak pouches. I believe there are 
some "for home" commercial alternatives, although probably for frozen storage. 
Worth exploring "out of the lab" alternatives.
René J.

--- On Thu, 8/13/09, Susan Raibley  wrote:


From: Susan Raibley 
Subject: [Histonet] Specimen Storage
To: histonet@lists.utsouthwestern.edu
Date: Thursday, August 13, 2009, 3:18 PM


I work for a research company and am looking at ideas for storage of specimens. 
We currently use Bitran bags to keep the extra parts with some formalin and 
then heat seal them in the Kapak heat seal bags. The Bitran bags are getting so 
expensive and tend to leak. Does anyone have a better system for long term 
storage of multiple animal specimens? Thanks!
 
Susan Bincsik, HT (ASCP)

__
Do You Yahoo!?
Tired of spam?  Yahoo! Mail has the best spam protection around 
http://mail.yahoo.com
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet




___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] X-gal staining

2009-08-13 Thread Nicholas David Evans
Hello,

I was wondering whether anyone might advise me on X-gal staining. 

I am looking at the expression of LacZ knocked into the locus of our gene
of interest. We cryoembed, take sections and stain for beta-galactosidase
activity using X-gal. The blue stain is often punctuate and noticeably
limited to the nucleus, whereas in other areas the staining is diffuse and
appears throughout the cytoplasm of the cells. I have guessed that this
may be related to the level of expression; i.e. that in cells with a low
reporter activity beta-gal is limited to the nucleus, but that at higher
expression the whole cell becomes riddled with it. If anyone knows
anything about the subcellular distribution/localisation of beta-gal in
mammalian cells, or can direct me to some good literature I would be
grateful.

Best wishes
Nick
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Specimen Storage

2009-08-13 Thread Susan Raibley
I work for a research company and am looking at ideas for storage of specimens. 
We currently use Bitran bags to keep the extra parts with some formalin and 
then heat seal them in the Kapak heat seal bags. The Bitran bags are getting so 
expensive and tend to leak. Does anyone have a better system for long term 
storage of multiple animal specimens? Thanks!
 
Susan Bincsik, HT (ASCP)

__
Do You Yahoo!?
Tired of spam?  Yahoo! Mail has the best spam protection around 
http://mail.yahoo.com
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Re: Freezing in Hexane

2009-08-13 Thread Robert Richmond
Dorothy Murphy Traczyk at Murphy-Traczyk & Associates in Point
Pleasant, NJ asks about using hexane for snap-freezing.

I wouldn't want any of the hexanes (there are several isomers) or
2-methylbutane around my lab because of the explosion hazard if I
could avoid it.

Look up 3M Novec Engineered Fluid HFE-7100 (methyl nonafluoroisobutyl
ether) in the Histonet archives (accessible through Google). Probably
usable for this purpose, and not flammable.

If you do this, please report your experience to Histonet - several of
us on here are interested.

Bob Richmond
Samurai Pathologist
Knoxville TN

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Picric Acid

2009-08-13 Thread Diane Gerjets

Hello everyone!
I would like to know what all of you are doing now that 
picric acid is so hard to get? We use it for bouin's,  trichrome and 
gram stain. I know we can buy these already made up, but we wanted to 
know if there might be other alternatives. I'll be off tomorrow 
(state  fair time), but will check my e-mail first thing monday 
morning. Thank-you in advance for all your help!

Diane


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] advice about bone section please

2009-08-13 Thread Wei-Hsiang Huang
Hi all, I'm planning to do paraffin embed section on mouse joint (E12~P10)
to detect the GFP-tagged protein expression. Since bone has
autofluorescence, I'm wondering whether IHC would be a good choice for
postnatal bone, and can I do immunofluorescence on joint in E12~16 mouse
without having autofluorescence effect?

I've tried cryosection (10 micrometer) but the bone detached and doesn't
give me good morphology so I decided to try paraffin.

thank you all in advance.

W
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: [Histonet] optimal IHC thickness

2009-08-13 Thread Rene J Buesa
I always used 3-4µm and prefer HIER over enzymes.
René J.

--- On Thu, 8/13/09, Katelin Lester  wrote:


From: Katelin Lester 
Subject: [Histonet] optimal IHC thickness
To: histonet@lists.utsouthwestern.edu
Date: Thursday, August 13, 2009, 10:24 AM


Hi everyone,

I am staining lymph nodes for staging of breast cancer with CKAE1/AE3 and
would like to know what everyone is cutting this type of slide at.



I searched the archives and my understanding is that, for IHC, how thick the
sections are cut is not necessarily critical.  I typically cut all IHC at
4μm and I want to achieve the best results possible.



Also, on a side note, the Data Sheet suggests using Trypsin, but I have been
using Pepsin. Any comments or suggestions about time, quality of Trypsin vs.
Pepsin?



Thank you,

Katelin



Katelin Lester

Cutting Edge Histology Services, LLC

(503) 443-2157



___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet




___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Freezing in Hexane

2009-08-13 Thread Della Speranza, Vinnie
Hi Dorothy,
I've not used hexane. I think 2-methly butane is more commonly used if you are, 
as I suspect, snap freezing in a solvent chilled in liquid nitrogen. The 
solvent just needs to have a low freezing point. 2-methyl butane freezes at 
about - 150 degrees C. I do not know if hexane has a lower freezing point but 
you can determine that with an internet search.

My point in all of this is that you may have other choices for snap freezing if 
you can't get an answer to your original question re hexane as long as you are 
able to freeze the needed temperature.

Vinnie Della Speranza
Manager for Anatomic Pathology Services
165 Ashley Avenue Suite 309
Charleston, SC 29425
tel. 843-792-6353
fax. 843-792-8974
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of tracz...@aol.com
Sent: Wednesday, August 12, 2009 12:47 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Freezing in Hexane

I have a procedure that refers to freezing a tissue sample in chilled  
Hexane.  When I look in a chemical catalogue I find there are several  formulas 
listed.  Any direction on which one to use would be greatly  appreciated.  
Thank you.
Dorothy
 
Dorothy Murphy Traczyk
Murphy-Traczyk & Associates LLC
PO Box 602
Point Pleasant, NJ 08742
_doro...@mtahistology.com_ (mailto:doro...@mtahistology.com) 
www.mtahistology.com
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] optimal IHC thickness

2009-08-13 Thread Katelin Lester
Hi everyone,

I am staining lymph nodes for staging of breast cancer with CKAE1/AE3 and
would like to know what everyone is cutting this type of slide at.

 

I searched the archives and my understanding is that, for IHC, how thick the
sections are cut is not necessarily critical.  I typically cut all IHC at
4μm and I want to achieve the best results possible.

 

Also, on a side note, the Data Sheet suggests using Trypsin, but I have been
using Pepsin. Any comments or suggestions about time, quality of Trypsin vs.
Pepsin?

 

Thank you,

Katelin

 

Katelin Lester

Cutting Edge Histology Services, LLC

(503) 443-2157

 

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


Re: [Histonet] Stain Disposal

2009-08-13 Thread Shelly Christenson
Sally, the "Hazardous Materials in the Histopathology Laboratory " 
Regulations,, Risks, Handling and Disposal  is a nice reference book to have. 
It can be purchased from Anatech LTD 1-800-ANATECH

Shelly Christenson HT(ASCP)
Veterinary Diagnostic Lab.
Kansas State University
1800 Denison Ave
Manhattan Ks 66506


>>> "Breeden, Sara"  8/12/2009 8:51 AM >>>
Looking for a one-source listing of how to dispose of stains (i.e.,
specials - carbol fuchsin, iodine, Tartrazine, etc.). Is there such a
list or reference? Thanks.

 

Sally Breeden, HT(ASCP)

NM Dept. of Agriculture

Veterinary Diagnostic Services

PO Box 4700

Albuquerque, NM  87106

505-841-2576

 

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu 
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet