Re: [Histonet] Negative Reagent Control

2012-07-18 Thread Angela Bitting
Our Prayers have been answered!!!

 Richard Cartun rcar...@harthosp.org 7/17/2012 7:04 PM 
Most of you know that I have been advocating for the elimination of the 
Negative Reagent Control when using a non-avidin-biotin detection system 
(polymer) in immunohistochemical testing.  In my opinion, it is a waste of 
healthcare dollars and, more importantly, precious patient specimen.  Last year 
at the NSH IHC Forum in Denver I met James Dvorak, MT(ASCP) from the College of 
American Pathologists.  We had a long discussion about this and he agreed to 
support my position within CAP.  With the support of James, and the help of Dr. 
Regan Fulton (from the CAP IHC Committee), the wording on the CAP Anatomic 
Pathology checklist for question ANP.22570 will be changed.  The new wording 
includes the following sentence:

Immunohistochemical tests using polymer-based detection systems (biotin-free) 
are sufficiently free of background reactivity to obviated the need for a 
negative reagent control and such controls may be omitted at the discretion of 
the laboratory director.

I announced this change at the 2012 NSH IHC/ISH Forum this past weekend in 
Windsor, CT to loud applause.  This one change stands to save the healthcare 
system millions of dollars.  Thank you Jim and Dr. Fulton for making this 
happen!

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



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RE: [Histonet] Negative Reagent Control

2012-07-18 Thread Martha Ward-Pathology
What wonderful news


 
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 Angela Bitting
Sent: Wednesday, July 18, 2012 7:26 AM
To: Richard Cartun; Histonet
Subject: Re: [Histonet] Negative Reagent Control

Our Prayers have been answered!!!

 Richard Cartun rcar...@harthosp.org 7/17/2012 7:04 PM 
Most of you know that I have been advocating for the elimination of the 
Negative Reagent Control when using a non-avidin-biotin detection system 
(polymer) in immunohistochemical testing.  In my opinion, it is a waste of 
healthcare dollars and, more importantly, precious patient specimen.  Last year 
at the NSH IHC Forum in Denver I met James Dvorak, MT(ASCP) from the College of 
American Pathologists.  We had a long discussion about this and he agreed to 
support my position within CAP.  With the support of James, and the help of Dr. 
Regan Fulton (from the CAP IHC Committee), the wording on the CAP Anatomic 
Pathology checklist for question ANP.22570 will be changed.  The new wording 
includes the following sentence:

Immunohistochemical tests using polymer-based detection systems (biotin-free) 
are sufficiently free of background reactivity to obviated the need for a 
negative reagent control and such controls may be omitted at the discretion of 
the laboratory director.

I announced this change at the 2012 NSH IHC/ISH Forum this past weekend in 
Windsor, CT to loud applause.  This one change stands to save the healthcare 
system millions of dollars.  Thank you Jim and Dr. Fulton for making this 
happen!

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



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[Histonet] IL5

2012-07-18 Thread Chiriboga, Luis
Does anyone on the net do or know of a lab that does  IL-5 IHC for 
clinical/diagnostic purposes?

TIA



Luis Chiriboga Ph.D, Director
OCS Experimental Pathology IHC Core Lab
NYU School of Medicine
Medical Science Building Room 124
646-501-6934
luis.chirib...@nyumc.org


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RE: [Histonet] Negative Reagent Control

2012-07-18 Thread Chiriboga, Luis
Outstanding!!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Richard Cartun
Sent: Tuesday, July 17, 2012 7:05 PM
To: Histonet
Subject: [Histonet] Negative Reagent Control

Most of you know that I have been advocating for the elimination of the 
Negative Reagent Control when using a non-avidin-biotin detection system 
(polymer) in immunohistochemical testing.  In my opinion, it is a waste of 
healthcare dollars and, more importantly, precious patient specimen.  Last year 
at the NSH IHC Forum in Denver I met James Dvorak, MT(ASCP) from the College of 
American Pathologists.  We had a long discussion about this and he agreed to 
support my position within CAP.  With the support of James, and the help of Dr. 
Regan Fulton (from the CAP IHC Committee), the wording on the CAP Anatomic 
Pathology checklist for question ANP.22570 will be changed.  The new wording 
includes the following sentence:

Immunohistochemical tests using polymer-based detection systems (biotin-free) 
are sufficiently free of background reactivity to obviated the need for a 
negative reagent control and such controls may be omitted at the discretion of 
the laboratory director.

I announced this change at the 2012 NSH IHC/ISH Forum this past weekend in 
Windsor, CT to loud applause.  This one change stands to save the healthcare 
system millions of dollars.  Thank you Jim and Dr. Fulton for making this 
happen!

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



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[Histonet] any news on CD4, CD8 IHC on FFPE mouse tissue?

2012-07-18 Thread Connolly, Brett M
I'm wondering if anyone has recommendations for CD4 and CD8 antibodies for FFPE 
mouse tissue. Looking through the archives I see there was only success on 
frozen tissues.

Has anything changed recently?? Or should I stick with CD3.

Thanks,
Brett

Brett M. Connolly, Ph.D.
Principal Scientist, Imaging Dept.
Merck  Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
brett_conno...@merck.com
T- 215-652-2501
F- 215-993-6803







Notice:  This e-mail message, together with any attachments, contains
information of Merck  Co., Inc. (One Merck Drive, Whitehouse Station,
New Jersey, USA 08889), and/or its affiliates Direct contact information
for affiliates is available at 
http://www.merck.com/contact/contacts.html) that may be confidential,
proprietary copyrighted and/or legally privileged. It is intended solely
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[Histonet] (no subject)

2012-07-18 Thread MaryK Mendell
I work in a small lab (office bldg) that has been turned into histolab.  We 
have a portable work station with a vent to out side. (roof)  I also have my 
VIP processor in this room which has the filter carbon (activated) on the 
processor. Where we have an issue is , on very windy days there seems to be a 
down draft that happens causing fumes to go into other offices (not ours). I 
have been looking into the air filter system by leica and one mercedes sells.  
They have a filter that can be changed every 6 months or so.  Has anyone used 
these with any sort of success rate?

Kate Mendell
Histopathology/Lab Manager

HOWARD S. GOLDBERG, M.D., INC
990 Paradise Road
Swampscott, MA  01907
TEL:  781.595.0151
FAX:  781.592.6780
kmend...@goldbergmd.netmailto:kmend...@goldbergmd.net
www.cosmesticdermcenter.comhttp://www.cosmesticdermcenter.com/
PRIVACY NOTICE: This e-mail message may contain confidential patient or other 
information belonging to the sender that is legally privileged.  This 
information is intended only for the use of the individual or authorized entity 
named above. The authorized recipient of this patient or other confidential 
information is prohibited from disclosing the information to any other party.  
If you have received this message in error, please notify the sender 
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[Histonet] RELIA Histology Job Update. Summertime in the South is Sizzlin hot and it's not just the temps!

2012-07-18 Thread Pam Barker
Hi Histonetters!!
I hope everyone is having a great day. Are you keeping cool on these hot
summer days?
Summertime in the South is Sizzlin hot and it's not just the temps!! 
I have some great new opportunities to tell you about:
I have full time permanent positions with some of the best employers in the
South.  They offer competitive salaries, great benefits and awesome crews to
work with.
Here is a list of the Sizzlin Summer Stuff!
Dermpath HistoTech - Atlanta, GA
Histology Tech evenings - Charlotte, NC
Histology Tech nights - Charlotte, NC
Histology Tech Days - Bristol, TN
Histology Tech Nights - Lafayette, LA
If you have any questions or know someone who might be interested please
contact me.  I would love to tell you about these opportunities or write
another referral check like I did today if you have a friend who might be
interested.
I hope to hear from you soon.  In the meantime grab some shade and a cool
drink! 

Thank You!
  
 
Pam Barker
President/Senior Recruiting Specialist-Histology
RELIA Solutions
Specialists in Allied Healthcare Recruiting
5703 Red Bug Lake Road #330
Winter Springs, FL 32708-4969
Phone: (407)657-2027
Cell: (407)353-5070
FAX: (407)678-2788
E-mail: rel...@earthlink.net 
www.facebook.com http://www.facebook.com/PamBarkerRELIA /PamBarkerRELIA
www.linkedin.com/in/reliasolutions
www.twitter.com/pamatrelia 


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[Histonet] NSH S/C

2012-07-18 Thread mequita praet
I am flying into Bellingham, WA on Friday Sept. 28th to attend the NSH S/C
(much cheaper than flying into Vancouver) at 2:38pm and am looking to share
a limo to Vancouver with 5 or 6 people. If you are interested please email
me. If I get enough interest, I will follow up and see if that is feasible.
Mequita Praet
mdpr...@gmail.com
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[Histonet] Re: Image Analysis for Fat Tissue

2012-07-18 Thread Nathanael Reveal
Hi Ateret,

You've got a few choices, some of which are free and some of which are
quite expensive.


In many soft tissue staining protocols, adipocytes show up as white, oval,
void spaces. Which is good!

Software like ImageJ http://rsbweb.nih.gov/ij/, or its more integrated
variant FIJI http://fiji.sc/wiki/index.php/Fiji (which stands for Fiji is
Just Image J) is an excellent place to start. They have very good and easy
to use measurement tools for area and number.


Unfortunately, the topic takes a turn for the complex. Cell number and cell
size (i.e. cell volume) can be subject to systematic bias due to section
orientation, section thickness, and related parameters. This may cause
under or over estimation of the data. This brings us to
Stereologyhttp://en.wikipedia.org/wiki/Stereology,
the science of estimating data from 2d cross-sections of 3d structures.

Say for example, you're sectioning at 5 microns. The 2d profiles (i.e.
cross-sections) of a large adiopcyte will appear on many sections, but the
2d profile of a small adiopcyte will show up only once or twice. In this
way, if you count all the adipocyte profiles you see, you could be
overestimating the number of adipocytes. You could be counting some
adiopocytes more than once.

There are standard techniques for estimating the total number of cells in a
region and the mean volume of a group of cells. The Optical Fractionator
estimates the total number of cells. The Rotator estimates mean cell
volume. These tools are found in most stereology systems, commercial or
free. The drawback to these methods are that they require specialized
commercial software and a microscope capable of monitoring real-time
position in X, Y, and Z. This is commonly done with either a motorized
stage or encoded stage.


Some practical alternatives you could implement with ImageJ may be:

1. Measure Adipose Volume. That is the area of adipose tissue measured
over a set of serial sections. The Delesse
principlehttp://en.wikipedia.org/wiki/Stereology(again from
Stereology) says that area fractions are proportional to volume
fractions in a set of serial sections. So no special hardware or random
sampling is required.

2. Take care to only count nucleated adipocyte profiles. This helps
minimize the problem of overcounting in serial sections.

3. Count adipocytes in sections that are not adjacent. Meaning, cut 5
micron sections but make sure the sections you count are far enough apart
that you won't see the cross-sections from the same adipocyte.

4. As far as measuring the volume of individual adipocytes, you might be
able use the shortest diameter of the nucleated adipocyte profiles in you
see in your sections. This is a tricky one and very much subject to the
shape of your adipocyte population.


As always, you'll do well to mimic the methods of those that have performed
similar work in the past. This will make it easier for reviewers to
understand your methods and comment constructively on your paper. You might
find this Google Scholar
searchhttp://scholar.google.com/scholar?as_ylo=2008q=adipocyte+volume+numberhl=enas_sdt=0,43helpful.
It covers references to adipocyte volume and adipocyte number
since 2008.


Best of Luck,
Nathanael


--
Nathanael Reveal, CEO
BIOQUANT Image Analysis Corporation

5611 Ohio Avenue, Nashville, TN 37209
phone: 615-350-7866, toll free: 800-221-0549, fax: 615-350-7282

email: nathan...@bioquant.com, web: www.bioquant.com
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[Histonet] Hold IHC overnight

2012-07-18 Thread Sarah Dysart
Just found out I have to go to a meeting in 2 hours for the rest of the day (I 
haven't even eaten lunch yet).  I do IHC manually, they just got done cooling 
off from HIER...I can store them overnight in buffer right?
Just double checking myself as this run is an antibody validation run...
-S-

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] RE: Image analysis for fat tissue

2012-07-18 Thread Jerry Ricks

Hi,

That is a pretty common kind of measurement.


You will need a digital camera attached to your microscope, and a stage 
micrometer.  You can then use the free software Image-J to get area 
measurements.  If you have some extra money Image-Pro software from Media 
Cybernetics is the deluxe way to go.  

Jerry Ricks
Research Scientist
University of Washington
Department of Pathology

 From: ater...@migal.org.il
 To: histonet@lists.utsouthwestern.edu
 Date: Wed, 18 Jul 2012 11:20:42 +
 Subject: [Histonet] Image analysis for fat tissue
 
 Dear Histonet members
 I'm interested in image analysis of mice fat tissue, I would like to quantify 
 number
 Of cells per area and average cell size.
 Does anyone know a software (+instructions/ lucid manual) which does that?
 Many thanks!
 
 -- Best regards --
 Ateret Shabtay-Yanai
 Migal- Galilee Technology Center
 Southern Industrial Zone- kiryat Smona
 P.O.B 831 Kiryat Shmona 11016
 Tel: +972-46955002
 Mobile: +972-547946460
 Email: ater...@migal.org.il
 
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[Histonet] Black Biopsy Paper

2012-07-18 Thread Rebecca LeVier
I am wondering if anyone out there is using black biopsy paper to give to 
offices to place the biopsy on prior to putting it into formalin? It looks kind 
of like construction paper. If you are using this can you please give me a list 
of pros and cons associated with it?

Thanks,
Becky


Disclaimer Note: The information in this message with any attachment to it, may 
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...

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[Histonet] RE: Hold IHC overnight

2012-07-18 Thread Goins, Tresa
I vote No - this run would be valid only if you held all future slides 
overnight after HIER.  

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sarah Dysart
Sent: Wednesday, July 18, 2012 11:44 AM
To: histonet
Subject: [Histonet] Hold IHC overnight

Just found out I have to go to a meeting in 2 hours for the rest of the day (I 
haven't even eaten lunch yet).  I do IHC manually, they just got done cooling 
off from HIER...I can store them overnight in buffer right?
Just double checking myself as this run is an antibody validation run...
-S-

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] RE: Black Biopsy Paper

2012-07-18 Thread Connolly, Brett M
Becky,  

We have used this paper. What I found is that when submersed in the formalin 
the black dye leaches out of the paper and the portion of the tissue touching 
the paper turned somewhat black. These were tissues left on the paper and in 
formalin overnight. Since I never processed that tissue I don't know if the 
black washes out during processing.

Brett

Brett M. Connolly, Ph.D.
Principal Scientist, Imaging Dept.
Merck  Co., Inc.
PO Box 4, WP-44K
West Point, PA 19486
brett_conno...@merck.com
T- 215-652-2501
F- 215-993-6803




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rebecca LeVier
Sent: Wednesday, July 18, 2012 2:26 PM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Black Biopsy Paper

I am wondering if anyone out there is using black biopsy paper to give to 
offices to place the biopsy on prior to putting it into formalin? It looks kind 
of like construction paper. If you are using this can you please give me a list 
of pros and cons associated with it?

Thanks,
Becky


Disclaimer Note: The information in this message with any attachment to it, may 
be privileged and protected from disclosure. If the reader of this message is 
neither the intended recipient, nor an employee or agent responsible for 
delivering this message to the intended recipient, then you are hereby notified 
that any dissemination, distribution, unauthorized use, or copying of this 
communication is strictly prohibited. If you have received this communication 
in error, please notify us immediately by replying to this message and deleting 
it from your computer. Thank you.


...

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Re: [Histonet] RE: Hold IHC overnight

2012-07-18 Thread Erin and Jesse
I agree 



On Jul 18, 2012, at 2:35 PM, Goins, Tresa tgo...@mt.gov wrote:

 I vote No - this run would be valid only if you held all future slides 
 overnight after HIER.  
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sarah Dysart
 Sent: Wednesday, July 18, 2012 11:44 AM
 To: histonet
 Subject: [Histonet] Hold IHC overnight
 
 Just found out I have to go to a meeting in 2 hours for the rest of the day 
 (I haven't even eaten lunch yet).  I do IHC manually, they just got done 
 cooling off from HIER...I can store them overnight in buffer right?
 Just double checking myself as this run is an antibody validation run...
 -S-
 
 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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RE: [Histonet] RE: Hold IHC overnight

2012-07-18 Thread Blazek, Linda
But only because it's a validation run.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Erin and Jesse
Sent: Wednesday, July 18, 2012 3:35 PM
To: Goins, Tresa
Cc: histonet
Subject: Re: [Histonet] RE: Hold IHC overnight

I agree 



On Jul 18, 2012, at 2:35 PM, Goins, Tresa tgo...@mt.gov wrote:

 I vote No - this run would be valid only if you held all future slides 
 overnight after HIER.  
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sarah Dysart
 Sent: Wednesday, July 18, 2012 11:44 AM
 To: histonet
 Subject: [Histonet] Hold IHC overnight
 
 Just found out I have to go to a meeting in 2 hours for the rest of the day 
 (I haven't even eaten lunch yet).  I do IHC manually, they just got done 
 cooling off from HIER...I can store them overnight in buffer right?
 Just double checking myself as this run is an antibody validation run...
 -S-
 
 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] RE: Hold IHC overnight

2012-07-18 Thread Jerry Ricks

No you can't do that.  If it were just a research IHC then you could give it a 
whirl, write down what you did and often it would work just fine depending on 
antigen and antibody.
But if you are validating an antibody for clinical lab you have to document you 
follow GLP SOP every time else you messed up.  

There's no getting around it.  You are just going to have to run the IHC stain 
again.

Jerry Ricks

 From: sdys...@mirnarx.com
 To: histonet@lists.utsouthwestern.edu
 Date: Wed, 18 Jul 2012 17:44:12 +
 Subject: [Histonet] Hold IHC overnight
 
 Just found out I have to go to a meeting in 2 hours for the rest of the day 
 (I haven't even eaten lunch yet).  I do IHC manually, they just got done 
 cooling off from HIER...I can store them overnight in buffer right?
 Just double checking myself as this run is an antibody validation run...
 -S-
 
 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] automated H+E and cover slipper

2012-07-18 Thread Joe Hardin

Hi All,
I will be trying out new H+E autostainers and cover slippers soon. Does 
anyone have a favorite, and why? Thanks for your responses.


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RE: [Histonet] automated H+E and cover slipper

2012-07-18 Thread Harrison, Sandra C.
Leica Autostainer XL with CV5030 coverslipper and transfer station.  

This has been a real timesaver for us.  It automatically moves the
slides from the stainer to the coverslipper.  It has been relatively
trouble free.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joe
Hardin
Sent: Wednesday, July 18, 2012 3:23 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] automated H+E and cover slipper

Hi All,
I will be trying out new H+E autostainers and cover slippers soon. Does
anyone have a favorite, and why? Thanks for your responses.


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RE: [Histonet] automated H+E and cover slipper

2012-07-18 Thread Elizabeth Chlipala
We have a Sakura Tissue Tek Prisma and Glas coverslipper we really like it.  
It's a workhorse.

Liz

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

Ship to address:

1567 Skyway Drive, Unit E
Longmont, CO 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joe Hardin
Sent: Wednesday, July 18, 2012 2:23 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] automated H+E and cover slipper

Hi All,
I will be trying out new H+E autostainers and cover slippers soon. Does
anyone have a favorite, and why? Thanks for your responses.


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RE: [Histonet] automated H+E and cover slipper

2012-07-18 Thread Bea DeBrosse-Serra
I second on that!

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 Harrison, 
Sandra C.
Sent: Wednesday, July 18, 2012 1:44 PM
To: Joe Hardin; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] automated H+E and cover slipper

Leica Autostainer XL with CV5030 coverslipper and transfer station.  

This has been a real timesaver for us.  It automatically moves the slides from 
the stainer to the coverslipper.  It has been relatively trouble free.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joe Hardin
Sent: Wednesday, July 18, 2012 3:23 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] automated H+E and cover slipper

Hi All,
I will be trying out new H+E autostainers and cover slippers soon. Does anyone 
have a favorite, and why? Thanks for your responses.


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Re: [Histonet] (no subject)

2012-07-18 Thread Jennifer MacDonald
It is added to formaldehyde to prevent polymerization of the formaldehyde.




Bader Siddiki bade...@gmail.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
07/17/2012 01:44 PM

To
Rene J Buesa rjbu...@yahoo.com
cc
histonet Histonet@lists.utsouthwestern.edu, Kelly Boyd 
kdboydhi...@yahoo.com
Subject
Re: [Histonet] (no subject)






Hello
 Methanol is added to reagent alcohol (ethyl alcohol) so that people do 
not
use for drinking purpose and for tax purposes. Alcohol (ethyl alcohol) has
federal tax just like liquor.
One can buy pure alcohol, but you have keep inventory and make sure it is
not misused.
Bader

On Tue, Jul 17, 2012 at 1:28 PM, Rene J Buesa rjbu...@yahoo.com wrote:

 To prevent oxidation of those 2 reagents
 René J.


 
 From: Kelly Boyd kdboydhi...@yahoo.com
 To: histonet Histonet@lists.utsouthwestern.edu
 Sent: Tuesday, July 17, 2012 1:16 PM
 Subject: [Histonet] (no subject)

 Since there is discussion of formalin and methanol, I would like to ask
 everyone.Why would a vendor add methanol to their reagent alcohol 
and
 their 10% buffered formalin?

 What are the advantages/disadvantages to the tissue especially for
 processing?

 Kelly
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-- 
If any Q's please feel free to contact us
Have a nice day/weekend
Mit freundlichen Grüßen / With Kind Regards /
avec l'aimable ce qui concerne
Met vriendelijke groeten
種とについて
Bader
Bader B Siddiki, PhD
Executive director,
Research and development
ImmunoBioScience Corp. (IBSC)
Phone: + 1 425 367 4601
Fax: + 1 425 367 4817
cell (mobile) phone: + 1 425 314 0199
e-mail address: bade...@gmail.com
Web site: www.ImmunoBioScience.Com
Marketing: phone: + 1 650 343 IBSC (4272)
E-mail: anitai...@aol.com
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RE: [Histonet] automated H+E and cover slipper

2012-07-18 Thread WILLIAM DESALVO

Sakura Prisma w/ tape cover slip. It also is available w/ glass cover slip. 
Reliable, fast and a workhorse.

William DeSalvo, B.S., HTL(ASCP)

  From: bdebrosse-se...@isisph.com
 To: sandra.harris...@va.gov; har...@oncology.wisc.edu; 
 histonet@lists.utsouthwestern.edu
 Date: Wed, 18 Jul 2012 14:18:53 -0700
 Subject: RE: [Histonet] automated H+E and cover slipper
 CC: 
 
 I second on that!
 
 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 Harrison, 
 Sandra C.
 Sent: Wednesday, July 18, 2012 1:44 PM
 To: Joe Hardin; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] automated H+E and cover slipper
 
 Leica Autostainer XL with CV5030 coverslipper and transfer station.  
 
 This has been a real timesaver for us.  It automatically moves the slides 
 from the stainer to the coverslipper.  It has been relatively trouble free.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joe Hardin
 Sent: Wednesday, July 18, 2012 3:23 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] automated H+E and cover slipper
 
 Hi All,
 I will be trying out new H+E autostainers and cover slippers soon. Does 
 anyone have a favorite, and why? Thanks for your responses.
 
 
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 Histonet@lists.utsouthwestern.edu
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