Re: [Histonet] Stripping antibodies

2011-10-31 Thread John Kiernan
With quantum dots and a modern fluorescence microscope with channels it 
should be possible to label 2 or 3 antigens simultaneously, if you have all the 
right primaries and labelled secondaries. The company that sells you the 
quantum dot labelled secondaries or other amplification reagents should be in a 
position to tell you exactly what to do. Do they refund your hard-earned grant 
money if their expensive product fails to perform as advertized? 
 
Immunohistochemistry with non-fluorescent colours (available in brown, black, 
red and various blues) has advantages: 
(a) You do not need a fluorescence microscope. Modern fluorescence microscopes 
are very expensive; the old ones from the 1960s are no longer be good enough to 
provide publication-quality pictures.
(b) Immunostained slides can be kept for many years in boxes at room 
temperature.
(c) The colours do not fade in permanently mounted preparations. 
(c) You are not bound to use a commercially sold kit, which may not be 
optimized for your research.
 
If you go by the book (= any book with references that you can follow up), you 
will do your multiple immunostains intelligently. Never follow a set of 
instructions without knowing or questioning the reason for ever step. 
 
John Kiernan 
Anatomy, UWO 
London, Canada. 
= = = 
 On 30/10/11, Claire Weston cwes...@valasciences.com wrote:

 
 
 
 Thank you everyone for your advice, I really appreciate it!  I am doing a 
 multiplex immunofluorescent assay (4 channels) and I am planning to strip the 
 antibodies and reprobe with a second round of antibodies.  The antibodies are 
 labelled with quantum dots so I am not sure how that will influence things, 
 but luckily I won't have the DAB problem several of you mentioned.  I think I 
 will try several of these techniques and evaluate which works the best.
  
 Thanks again for all your help,
  
 Claire  
 
 --- jkier...@uwo.ca wrote:
 
 From: John Kiernan jkier...@uwo.ca
 To: histonet@lists.utsouthwestern.edu, cwes...@valasciences.com
 Cc: Amos Brooks amosbro...@gmail.com
 Subject: Re: [Histonet] Stripping antibodies
 Date: Sun, 30 Oct 2011 12:09:58 -0400
 
 
   
 Antibodies are quite easily removed by acidity - pH 1 to 2. This also removes 
 enzyme-antibody conjugates. The coloured products of the enzyme histochemical 
 reactions are generally not affected. The brown oxidation product of DAB 
 (from peroxidase) and the blue products from bromochloroindoxyl/tetrazolium 
 methods (for alkaline phosphatase) are very stable. This is good: you can 
 remove all the primary and enzyme-labelled antibodies without losing track of 
 the stained antigen in the section. A second immunostaining, with a 
 differently coloured end-product can follow.  If you use AEC as a peroxidase 
 chromogen (red), it should be for the last immunohistochemical procedure, and 
 you will have to use an aqueous mounting medium. The AEC oxidation product 
 dissolves in alcohol and other organic solvents.
  
 Amos suggests a strong oxidation (acid permanganate followed by oxalic acid 
 to remove brown manganese dioxide) to get rid of the insoluble brown 
 oxidation product of DAB. Is this what you want?  This oxidation converts the 
 sulphur-containing amino acids, including cystine -S-S- links, to sulphonic 
 acids, which attract cationic dyes even at pH 1. This oxidation couuld 
 seriously modify the epitopes for the next applied primary antibody.
  
 Multicolour immunohistochemistry has been a developed technology for several 
 years. Any lab needing to do such work needs to take training courses 
 (hundreds of dollars) or buy a book (tens of dollars).  The one by Chris van 
 der Loos, Immunoenzyme Multiple Staining Methods, Oxford, UK: Bios,  1999, is 
 very good.
  
 John Kiernan
 Anatomy, UWO 
 London, Canada 
 = = = =
 On 29/10/11, Amos Brooks amosbro...@gmail.com wrote: 
 
  
  Hi,
  Stripping sites are usually found in the more seedy areas of large
  cities ... Oh wait you meant ... nevermind :-) If you developed the reaction
  with DAB, you may be in a difficult position. DAB is a really strong
  reaction. You might try a Mallory bleach to remove it. 0.3% sulfuric acid in
  5% potassium premanganate for 5 min followed by 5% oxalic acid until it is
  clear (usually a couple of minutes). Unfortunately, I am not sure what
  effect this will have on the epitopes you are looking for, but this is
  usually what is used to clean precipitated DAB from instruments it should
  work on the tissue too.
  If you use another chromogen such as AEC it is much easier (to many
  people's dismay) to remove this end product. Using alkaline phosphatase will
  be easy to remove the chromogens as well. It would also be very easy to do
  this with fluorescent tags too. Just remove the coverslip and dip the slide
  in ethanol and it will remove the colored end product. Then just start over
  for the new antigen.
  
  Good luck,
  Amos
  
  On Fri, Oct 28, 2011 at 11:50 AM, 

RE: [Histonet] SALARY

2011-10-31 Thread Heath, Nancy L.
Histotechnologists are the most valuable employees in the laboratory
today!

THANK YOU DR. CARTUN!! 

Nancy Heath, HT (ASCP)
Neuropathology Technician
Neuropathology Department
Rhode Island Hospital
President - Rhode Island Society for Histotechnology


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Richard
Cartun
Sent: Friday, October 28, 2011 12:52 PM
To: kcasti...@frii.com; Histonet@lists.utsouthwestern.edu; Caroline
Pratt
Subject: RE: [Histonet] SALARY

I think that's low.  If you find a good candidate with years of
experience I would pay them whatever it takes to get them in the door.
It's like Free Agency in baseball; if you want a good player, you need
to put the money on table.  Histotechnologists are the most valuable
employees in the laboratory today! 

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


 Pratt, Caroline caroline.pr...@uphs.upenn.edu 10/28/2011 9:21 AM

I would say $28 to $32 dollars an hour depending on experience and
education.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
kcasti...@frii.com 
Sent: Friday, October 28, 2011 7:54 AM
To: Histonet@lists.utsouthwestern.edu 
Subject: [Histonet] SALARY

HI EVERYONE,

WOULD LIKE TO KNOW WHAT LEAD TECHS AND SUPERVISORS ARE GETTING PAID 
THESE DAYS.  HAVE A FELLOW HISTO PERSON THAT IS RUNNING THEIR OWN DERM 
LAB AND DOING MOHS ALSO.  THANKS FOR YOUR HELP.  KRISTY

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RE: [Histonet] SALARY

2011-10-31 Thread Heath, Nancy L.
Just got offered a lead tech position, salary of $85600.00 in a private lab 
opened by a group of docs. Didn't take it because the health insurance plan 
they offered was lousey. 75% health covered with a 250.00 deductable, dental 
covered at 60% and no coverage for family or husbandwould of had to pay 
that out of pocket.
I'm in New England.


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of John Shelley
Sent: Friday, October 28, 2011 2:25 PM
To: Pratt, Caroline; Richard Cartun; kcasti...@frii.com; 
Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] SALARY

With all that said what are your going rates in this area that you are speaking.

Kind Regards!
 
John J Shelley




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pratt, Caroline
Sent: Friday, October 28, 2011 2:19 PM
To: Richard Cartun; kcasti...@frii.com; Histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] SALARY

If that is an option, I would agree, but non-profit teaching hospitals
have compensation ranges and grids according to education and
experience.  We keep every employee with the same education and skill
set at the same compensation for an equitable pay system.  If we feel
our employees are being under paid we will conduct a market analysis and
the rates will be increased for all applicable employees if the market
analysis justifies it.

Car :)

-Original Message-
From: Richard Cartun [mailto:rcar...@harthosp.org] 
Sent: Friday, October 28, 2011 12:52 PM
To: kcasti...@frii.com; Histonet@lists.utsouthwestern.edu; Pratt,
Caroline
Subject: RE: [Histonet] SALARY

I think that's low.  If you find a good candidate with years of
experience I would pay them whatever it takes to get them in the door.
It's like Free Agency in baseball; if you want a good player, you need
to put the money on table.  Histotechnologists are the most valuable
employees in the laboratory today! 

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


 Pratt, Caroline caroline.pr...@uphs.upenn.edu 10/28/2011 9:21 AM

I would say $28 to $32 dollars an hour depending on experience and
education.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
kcasti...@frii.com 
Sent: Friday, October 28, 2011 7:54 AM
To: Histonet@lists.utsouthwestern.edu 
Subject: [Histonet] SALARY

HI EVERYONE,

WOULD LIKE TO KNOW WHAT LEAD TECHS AND SUPERVISORS ARE GETTING PAID 
THESE DAYS.  HAVE A FELLOW HISTO PERSON THAT IS RUNNING THEIR OWN DERM 
LAB AND DOING MOHS ALSO.  THANKS FOR YOUR HELP.  KRISTY

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RE: [Histonet] SALARY

2011-10-31 Thread Heath, Nancy L.
I agree :)

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Breeden,
Sara
Sent: Friday, October 28, 2011 3:22 PM
To: Podawiltz, Thomas; Richard Cartun; kcasti...@frii.com;
Histonet@lists.utsouthwestern.edu; Caroline Pratt
Subject: RE: [Histonet] SALARY

I nominate Dr. Cartun as the Patron Saint for Histopathology.  We should
work on a statue and a Mission Statement for him...

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[Histonet] RE: Must be Monday...

2011-10-31 Thread Blazek, Linda
That's a hoot Sally!  I don't think that DST of old was even this past weekend. 
 For the past 3 years my processor changed on the DST of old and the powers 
that be told me it was impossible because that wasn't programmed into my 
processor's data.  This year I forgot about it and it didn't change on the old 
date.  
Linda

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Breeden, Sara
Sent: Monday, October 31, 2011 8:33 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Must be Monday...

Here I sit, languishing as if I had nothing at all to do.  And why, you
ask, is that?  It seems that Daylight Savings Time of Olde has taken
command of my processor.  Nothing on any calendar I've got here in the
lab says anything about DST being a factor for this weekend - and, in
fact, my calendar says NEXT Sunday is DST.  So I have time to agitate
Histonet, having about 45 minutes left to entertain myself.  And it is
Halloween...

 

Sally Breeden, HT(ASCP)

New Mexico Department of Agriculture

Veterinary Diagnostic Services

1101 Camino de Salud NE

Albuquerque, NM  87102

505-383-9278 (Histology Lab)

 

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[Histonet] Florida Medical Directorship

2011-10-31 Thread Hale, Meredith
What are the true regulations' in Florida as far as time required for a
Medical Director to be on site at the lab ?  I am finding conflicting
information and would like to know what is truly required. Thanks 

 

Meredith Hale HT  (ASCP)cm

Operations Liaision Director and Education Coordinator 

 

Caris Life Sciences

6655 North MacArthur Blvd. 

Irving , Texas 75039

Office: 214-596-2219

Cell: 469-648-8253

 

 

 

 

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[Histonet] Problems with Frozen tissues

2011-10-31 Thread Igor Deyneko
I'm looking for some advice on frozen tissues. This is the first time I'm
doing it. All the tissues: skin, lungs, spleen, liver, and pancreas cut
well onto special Gold Plus slides from Fisher. Then, when I was ready to
stain the slides, i air dried them fro an hour and wanted to do HE and
Beta-Gal, all the tissues fell off slides. Can anyone suggest any tips on
preventing this mischief?
Thank you in advance.
Igor Deyneko
Infinity Pharmaceuticals
Cambridge, MA
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[Histonet] Stripping antibodies

2011-10-31 Thread C.M. van der Loos
Amos and John,
I do not agree with John saying that antibodies could be easily removed by 
acidity pH1-2. High affinity primaries will stay at the tissue section nicely 
bound to the epitope. Try for example SMA, clone 1A4 antibody in the usual 
dilution. After this incubation strip off the antibody by glycin-HCl buffer pH2 
and then apply an anti-mouse detection system. You will stain SMA for sure. The 
only way to get antibodies off is 10 min boiling with citrate pH6.0 or so, as 
in HIER. I have described that in JOH in 2008, vol 31, pp. 119-127, being the 
basis of an AP sequential double staining.

Chris van der Loos
Academic Medical Center
Dept. of Pathology M2-230
Amsterdam
The Netherlands

Date: Sun, 30 Oct 2011 12:09:58 -0400
From: John Kiernan jkier...@uwo.ca
Subject: Re: [Histonet] Stripping antibodies
To: histonet@lists.utsouthwestern.edu, cwes...@valasciences.com
Cc: Amos Brooks amosbro...@gmail.com
Message-ID: 7640acec48487.4ead3...@uwo.ca
Content-Type: text/plain; CHARSET=US-ASCII

 
Antibodies are quite easily removed by acidity - pH 1 to 2. This also removes 
enzyme-antibody conjugates. The coloured products of the enzyme histochemical 
reactions are generally not affected. The brown oxidation product of DAB (from 
peroxidase) and the blue products from bromochloroindoxyl/tetrazolium methods 
(for alkaline phosphatase) are very stable. This is good: you can remove all 
the primary and enzyme-labelled antibodies without losing track of the stained 
antigen in the section. A second immunostaining, with a differently coloured 
end-product can follow.  If you use AEC as a peroxidase chromogen (red), it 
should be for the last immunohistochemical procedure, and you will have to use 
an aqueous mounting medium. The AEC oxidation product dissolves in alcohol and 
other organic solvents.
 
Amos suggests a strong oxidation (acid permanganate followed by oxalic acid to 
remove brown manganese dioxide) to get rid of the insoluble brown oxidation 
product of DAB. Is this what you want?  This oxidation converts the 
sulphur-containing amino acids, including cystine -S-S- links, to sulphonic 
acids, which attract cationic dyes even at pH 1. This oxidation couuld 
seriously modify the epitopes for the next applied primary antibody.
 
Multicolour immunohistochemistry has been a developed technology for several 
years. Any lab needing to do such work needs to take training courses (hundreds 
of dollars) or buy a book (tens of dollars).  The one by Chris van der Loos, 
Immunoenzyme Multiple Staining Methods, Oxford, UK: Bios,  1999, is very good.
 
John Kiernan
Anatomy, UWO
London, Canada

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[Histonet] RE: Must be Monday...

2011-10-31 Thread Beckham, Sharon
Yes it was this past weekend back when.  My alarm clock went to DST Sunday 
morning.
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Blazek, Linda
Sent: Monday, October 31, 2011 7:40 AM
To: 'Breeden, Sara'; Histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Must be Monday...

That's a hoot Sally!  I don't think that DST of old was even this past weekend. 
 For the past 3 years my processor changed on the DST of old and the powers 
that be told me it was impossible because that wasn't programmed into my 
processor's data.  This year I forgot about it and it didn't change on the old 
date.  
Linda

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Breeden, Sara
Sent: Monday, October 31, 2011 8:33 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Must be Monday...

Here I sit, languishing as if I had nothing at all to do.  And why, you ask, is 
that?  It seems that Daylight Savings Time of Olde has taken command of my 
processor.  Nothing on any calendar I've got here in the lab says anything 
about DST being a factor for this weekend - and, in fact, my calendar says NEXT 
Sunday is DST.  So I have time to agitate Histonet, having about 45 minutes 
left to entertain myself.  And it is Halloween...

 

Sally Breeden, HT(ASCP)

New Mexico Department of Agriculture

Veterinary Diagnostic Services

1101 Camino de Salud NE

Albuquerque, NM  87102

505-383-9278 (Histology Lab)

 

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[Histonet] RE: SALARY

2011-10-31 Thread Mayer,Toysha N
Add location to that.  $28-32 is great for places that do not have an abundant 
supply of techs.  Here in Houston, we have 2 schools and a very large medical 
center.  Entry level techs are not hard to find.  Graduates expect $23-28 
minimum depending on facility.  
In other states, neighboring Louisiana and such, they expect $21-24.  It just 
depends on the cost of living in the area.
Entry supervisors earn $30+ an hour, but again, it is based on cost of living 
and work conditions.  Reference labs pay more, but expect more.

My first supervisor job paid $32, and I worked like crazy.  It wasn't worth it. 
You get what you pay for though, and in this economic climate, the high 
salaries are not as plentiful as they once were.

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




Message: 6
Date: Fri, 28 Oct 2011 12:52:23 -0400
From: Richard Cartun rcar...@harthosp.org
Subject: RE: [Histonet] SALARY
To: kcasti...@frii.com,Histonet@lists.utsouthwestern.edu,
Caroline Pratt caroline.pr...@uphs.upenn.edu
Message-ID: 4eaaa586.7400.007...@harthosp.org
Content-Type: text/plain; charset=US-ASCII

I think that's low.  If you find a good candidate with years of experience I 
would pay them whatever it takes to get them in the door.  It's like Free 
Agency in baseball; if you want a good player, you need to put the money on 
table.  Histotechnologists are the most valuable employees in the laboratory 
today! 

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


 Pratt, Caroline caroline.pr...@uphs.upenn.edu 10/28/2011 9:21 AM 
I would say $28 to $32 dollars an hour depending on experience and education.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
kcasti...@frii.com 
Sent: Friday, October 28, 2011 7:54 AM
To: Histonet@lists.utsouthwestern.edu 
Subject: [Histonet] SALARY

HI EVERYONE,

WOULD LIKE TO KNOW WHAT LEAD TECHS AND SUPERVISORS ARE GETTING PAID 
THESE DAYS.  HAVE A FELLOW HISTO PERSON THAT IS RUNNING THEIR OWN DERM 
LAB AND DOING MOHS ALSO.  THANKS FOR YOUR HELP.  KRISTY

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RE: [Histonet] SALARY

2011-10-31 Thread joelle weaver

I know the cost of living is greater on the east coast, but that sounds good to 
me. The insurance is not better, and as an HTL I make less than 1/2 of that! 
Things are determined by the market I realize, but all these postings are sure 
making me feel bad and also realize that I am not marketing myself well

Joelle Weaver MAOM, BA, (HTL) ASCP
  Date: Mon, 31 Oct 2011 06:29:12 -0400
 From: nhe...@lifespan.org
 To: jshel...@sanfordburnham.org; caroline.pr...@uphs.upenn.edu; 
 rcar...@harthosp.org; kcasti...@frii.com; Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] SALARY
 CC: 
 
 Just got offered a lead tech position, salary of $85600.00 in a private lab 
 opened by a group of docs. Didn't take it because the health insurance plan 
 they offered was lousey. 75% health covered with a 250.00 deductable, dental 
 covered at 60% and no coverage for family or husbandwould of had to pay 
 that out of pocket.
 I'm in New England.
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of John Shelley
 Sent: Friday, October 28, 2011 2:25 PM
 To: Pratt, Caroline; Richard Cartun; kcasti...@frii.com; 
 Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] SALARY
 
 With all that said what are your going rates in this area that you are 
 speaking.
 
 Kind Regards!
  
 John J Shelley
 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pratt, 
 Caroline
 Sent: Friday, October 28, 2011 2:19 PM
 To: Richard Cartun; kcasti...@frii.com; Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] SALARY
 
 If that is an option, I would agree, but non-profit teaching hospitals
 have compensation ranges and grids according to education and
 experience.  We keep every employee with the same education and skill
 set at the same compensation for an equitable pay system.  If we feel
 our employees are being under paid we will conduct a market analysis and
 the rates will be increased for all applicable employees if the market
 analysis justifies it.
 
 Car :)
 
 -Original Message-
 From: Richard Cartun [mailto:rcar...@harthosp.org] 
 Sent: Friday, October 28, 2011 12:52 PM
 To: kcasti...@frii.com; Histonet@lists.utsouthwestern.edu; Pratt,
 Caroline
 Subject: RE: [Histonet] SALARY
 
 I think that's low.  If you find a good candidate with years of
 experience I would pay them whatever it takes to get them in the door.
 It's like Free Agency in baseball; if you want a good player, you need
 to put the money on table.  Histotechnologists are the most valuable
 employees in the laboratory today! 
 
 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
 
 
  Pratt, Caroline caroline.pr...@uphs.upenn.edu 10/28/2011 9:21 AM
 
 I would say $28 to $32 dollars an hour depending on experience and
 education.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
 kcasti...@frii.com 
 Sent: Friday, October 28, 2011 7:54 AM
 To: Histonet@lists.utsouthwestern.edu 
 Subject: [Histonet] SALARY
 
 HI EVERYONE,
 
 WOULD LIKE TO KNOW WHAT LEAD TECHS AND SUPERVISORS ARE GETTING PAID 
 THESE DAYS.  HAVE A FELLOW HISTO PERSON THAT IS RUNNING THEIR OWN DERM 
 LAB AND DOING MOHS ALSO.  THANKS FOR YOUR HELP.  KRISTY
 
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 have received this document in error and that any review, dissemination, 
 distribution, or copying of this message is strictly prohibited. If you have 
 received this 

[Histonet] RE: need help with TMA

2011-10-31 Thread Helen Fedor
Hello, Do 30 minutes at 37 degrees on a glass slide. take from oven and apply 
gentle pressure to center of block and slide complex, cool to RT and repeat 1 
or two times.

Helen

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Patricia F Lott
Sent: Friday, October 28, 2011 1:13 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] need help with TMA

We have recently started doing tissue microarrays.  The problem we have is that 
some of the small cores drop out after the first few sections.

I think my problem is in the step where we are supposed to melt the donor and 
recipient blocks together.  We tried 5 minutes at 37 degrees, and then  minutes 
at 60 degrees x3, with cooling to room temp in between.

Any suggestions?

Thanks,
Patty Lott, UAB
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RE: [Histonet] RE: SALARY

2011-10-31 Thread joelle weaver

Still sounds good to me, at my first supervisor's job ( the credentials I had 
at the time were HTL + Bachelor's), and I made less than $23 per hour and 
worked an average of 16 hours a day with no OT or comp time that was ever 
granted ( though promised). I guess I am just trying to say, count your 
blessings. Having a school near by really seems to impact the supply and demand 
and the general hiring environment. What I have noticed also is that when you 
go somewhere and the cost of living is less the tax burden is greater, so it 
has always seemed to come out in the wash. Anyhow, all these salary 
revelations have really made me think, thanks for the postings.

Joelle Weaver MAOM, BA, (HTL) ASCP
  From: tnma...@mdanderson.org
 To: histonet@lists.utsouthwestern.edu
 Date: Mon, 31 Oct 2011 09:25:58 -0500
 Subject: [Histonet] RE: SALARY
 
 Add location to that.  $28-32 is great for places that do not have an 
 abundant supply of techs.  Here in Houston, we have 2 schools and a very 
 large medical center.  Entry level techs are not hard to find.  Graduates 
 expect $23-28 minimum depending on facility.  
 In other states, neighboring Louisiana and such, they expect $21-24.  It just 
 depends on the cost of living in the area.
 Entry supervisors earn $30+ an hour, but again, it is based on cost of living 
 and work conditions.  Reference labs pay more, but expect more.
 
 My first supervisor job paid $32, and I worked like crazy.  It wasn't worth 
 it. 
 You get what you pay for though, and in this economic climate, the high 
 salaries are not as plentiful as they once were.
 
 Toysha N. Mayer, MBA, HT (ASCP)
 Instructor
 Program in Histotechnology
 School of Health Professions
 MD Anderson Cancer Center
 (713) 563-3481
 tnma...@mdanderson.org
 
 
 
 
 Message: 6
 Date: Fri, 28 Oct 2011 12:52:23 -0400
 From: Richard Cartun rcar...@harthosp.org
 Subject: RE: [Histonet] SALARY
 To: kcasti...@frii.com,Histonet@lists.utsouthwestern.edu,
   Caroline Pratt caroline.pr...@uphs.upenn.edu
 Message-ID: 4eaaa586.7400.007...@harthosp.org
 Content-Type: text/plain; charset=US-ASCII
 
 I think that's low.  If you find a good candidate with years of experience I 
 would pay them whatever it takes to get them in the door.  It's like Free 
 Agency in baseball; if you want a good player, you need to put the money on 
 table.  Histotechnologists are the most valuable employees in the laboratory 
 today! 
 
 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
 
 
  Pratt, Caroline caroline.pr...@uphs.upenn.edu 10/28/2011 9:21 AM 
 I would say $28 to $32 dollars an hour depending on experience and education.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
 kcasti...@frii.com 
 Sent: Friday, October 28, 2011 7:54 AM
 To: Histonet@lists.utsouthwestern.edu 
 Subject: [Histonet] SALARY
 
 HI EVERYONE,
 
 WOULD LIKE TO KNOW WHAT LEAD TECHS AND SUPERVISORS ARE GETTING PAID 
 THESE DAYS.  HAVE A FELLOW HISTO PERSON THAT IS RUNNING THEIR OWN DERM 
 LAB AND DOING MOHS ALSO.  THANKS FOR YOUR HELP.  KRISTY
 
 ___
 Histonet mailing list
 Histonet@lists.utsouthwestern.edu 
 http://lists.utsouthwestern.edu/mailman/listinfo/histonet 
 
 
 The information contained in this e-mail message is intended only for the 
 personal and confidential use of the recipient(s) named above. If the reader 
 of this message is not the intended recipient or an agent responsible for 
 delivering it to the intended recipient, you are hereby notified that you 
 have received this document in error and that any review, dissemination, 
 distribution, or copying of this message is strictly prohibited. If you have 
 received this communication in error, please notify us immediately by e-mail, 
 and delete the original message.
 
 
 
 
 --
 
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 End of Histonet Digest, Vol 95, Issue 34
 
 
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[Histonet] background checks required by AHCA

2011-10-31 Thread Nicole Tatum
I am currently filing out my ahca renewal application. There are many
changes and the form and I do not find it user friendly. Anyways here my
question: Medical directors and chief finicial officers or any person who
stands to gain profit must undergo a level 2 background screeening. On the
new app is states all empolyees and health care providers. I called acha
licensing division and they said only directors and so forth. But, on ahca
website statue 408(something, ill have to get exact number) when into
effect in 2010 that says all employees and newly hired employees must
underground background screening. So does all the arnp, pa, ht, and ma's
need to be screened because we have a lab?

Nicole Tatum, HT ASCP

http://ahca.myflorida.com/mchq/long_term_care/Background_Screening/BGS_WhoRequiredToBeScreened.pdf


taken directly from ahca site:

Employees and Contractors employed before August 1, 2010

Every employee/contractor must attest to meeting the requirements of this
chapter and agreeing to inform the employer immediately if arrested for
any of the disqualifying offenses while employed by the employer. [Section
435.05(2)]. This attestation must be maintained in the employee’s
personnel file. You may use the Affidavit of Compliance with Background
Screening to satisfy the attestation requirement.

If an employer becomes aware that an employee/contractor has been arrested
for a disqualifying offense, the employer must remove the
employee/contractor from contact with any vulnerable person that places
the employee/contractor in a role that requires background screening until
the arrest is resolved in a way that the employer determines that the
employee/contractor is still eligible for employment/contracting under
this chapter. [Section 435.06(2)(b)]


Rescreening




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[Histonet] Dako Pr on Ventana?

2011-10-31 Thread Orr, Rebecca
Hi Friends,
If anyone is using Dako  PR concentrate clone 1294 on a Ventana, could you 
please contact me separately?
I'd like some advice.
Thank you
Becky

Becky Orr CLA,HT(ASCP)QIHC
Technical Specialist
Anatomic Pathology
NorthShore University HealthSystem
847-570-2771

-Original Message-


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Re: [Histonet] Problems with Frozen tissues

2011-10-31 Thread Kim Donadio
Ive never just air dried my frozen sections. always put them in a fixative such 
as pen fix, a alcohol and or formalin mixture, something( depends on what your 
going to look for, test etc). That with using charged slides and never had too 
many problems with this. 
 
Kim



From: Igor Deyneko igor.deyn...@gmail.com
To: Histonet@lists.utsouthwestern.edu
Sent: Monday, October 31, 2011 9:56 AM
Subject: [Histonet] Problems with Frozen tissues

I'm looking for some advice on frozen tissues. This is the first time I'm
doing it. All the tissues: skin, lungs, spleen, liver, and pancreas cut
well onto special Gold Plus slides from Fisher. Then, when I was ready to
stain the slides, i air dried them fro an hour and wanted to do HE and
Beta-Gal, all the tissues fell off slides. Can anyone suggest any tips on
preventing this mischief?
Thank you in advance.
Igor Deyneko
Infinity Pharmaceuticals
Cambridge, MA
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[Histonet] slide labeling

2011-10-31 Thread Setlak, Lisa

Hi,
Just curious because this questions has come up multiple times from 
non-histology people so I thought I'd post it here. When labeling slides at 
microtomy what info do you include on the slide? I know the automated slide 
labelers that are out there will include patient name, surgical number etc.; 
but when handwriting slides as you cut what do you write on them? Currently we 
write the case number, part number and level as well as the cutters initials. 
After staining we put the permanent label on that has patient name and case 
number etc (hence two identifiers). Is there anyone out there who hand writes 
the patient name on the slide or a second identifier on it at the time of 
microtomy?
Thanks for your help,
Lisa

Lisa V.
Chg., IL

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[Histonet] stripping antibodies

2011-10-31 Thread MKing
If your antibodies are labeled with quantum dots and you strip the 
antibodies (e.g. with low pH) you will no longer have labeled targets in 
your tissue.  Not clear if you understood this from your post.


Message: 2
Date: Sun, 30 Oct 2011 11:58:19 -0700
From: Claire Weston cwes...@valasciences.com
Subject: Re: [Histonet] Stripping antibodies


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[Histonet] Re: Stripping antibodies

2011-10-31 Thread John Kiernan
Thanks Chris. I didn't know there were antibodies with such strong adhesion. 
 
John. 
 = = =
On 31/10/11, C.M. van der Loos c.m.vanderl...@amc.uva.nl wrote:

 
 Amos and John,
 I do not agree with John saying that antibodies could be easily removed by 
 acidity pH1-2. High affinity primaries will stay at the tissue section 
 nicely bound to the epitope. Try for example SMA, clone 1A4 antibody in the 
 usual dilution. After this incubation strip off the antibody by glycin-HCl 
 buffer pH2 and then apply an anti-mouse detection system. You will stain SMA 
 for sure. The only way to get antibodies off is 10 min boiling with citrate 
 pH6.0 or so, as in HIER. I have described that in JOH in 2008, vol 31, pp. 
 119-127, being the basis of an AP sequential double staining.
 
 Chris van der Loos
 Academic Medical Center
 Dept. of Pathology M2-230
 Amsterdam
 The Netherlands
 
 Date: Sun, 30 Oct 2011 12:09:58 -0400
 From: John Kiernan jkier...@uwo.ca
 Subject: Re: [Histonet] Stripping antibodies
 To: histonet@lists.utsouthwestern.edu, cwes...@valasciences.com
 Cc: Amos Brooks amosbro...@gmail.com
 Message-ID: 7640acec48487.4ead3...@uwo.ca
 Content-Type: text/plain; CHARSET=US-ASCII
 
  
 Antibodies are quite easily removed by acidity - pH 1 to 2. This also removes 
 enzyme-antibody conjugates. The coloured products of the enzyme histochemical 
 reactions are generally not affected. The brown oxidation product of DAB 
 (from peroxidase) and the blue products from bromochloroindoxyl/tetrazolium 
 methods (for alkaline phosphatase) are very stable. This is good: you can 
 remove all the primary and enzyme-labelled antibodies without losing track of 
 the stained antigen in the section. A second immunostaining, with a 
 differently coloured end-product can follow.  If you use AEC as a peroxidase 
 chromogen (red), it should be for the last immunohistochemical procedure, and 
 you will have to use an aqueous mounting medium. The AEC oxidation product 
 dissolves in alcohol and other organic solvents.
  
 Amos suggests a strong oxidation (acid permanganate followed by oxalic acid 
 to remove brown manganese dioxide) to get rid of the insoluble brown 
 oxidation product of DAB. Is this what you want?  This oxidation converts the 
 sulphur-containing amino acids, including cystine -S-S- links, to sulphonic 
 acids, which attract cationic dyes even at pH 1. This oxidation couuld 
 seriously modify the epitopes for the next applied primary antibody.
  
 Multicolour immunohistochemistry has been a developed technology for several 
 years. Any lab needing to do such work needs to take training courses 
 (hundreds of dollars) or buy a book (tens of dollars).  The one by Chris van 
 der Loos, Immunoenzyme Multiple Staining Methods, Oxford, UK: Bios,  1999, is 
 very good.
  
 John Kiernan
 Anatomy, UWO
 London, Canada
 
 

 
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[Histonet] RE: slide labeling

2011-10-31 Thread Goins, Tresa
Hi Lisa -

We hand write our labels, but do so prior to cutting sections.
  
The accession numbers [unique to every slide] are read from a printed data 
sheet and written on the slides.  This allows verification that the numbers 
match [slide and block] as the tissues are cut.  If the numbers are written at 
microtomy I see it as a source of possible labeling errors.

All blocks and slides are processed in numerical order so there is a number 
check at embedding, at cutting and at final labeling.


Tresa Goins
Veterinary Diagnostic Lab
South 19th and Lincoln
Bozeman, MT 59718
406-994-6353 - phone
406-994-6344 - fax

   

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Setlak, Lisa
Sent: Monday, October 31, 2011 10:09 AM
To: 'histonet@lists.utsouthwestern.edu'; 
'histonet-requ...@lists.utsouthwestern.edu'; 
'histonet-boun...@lists.utsouthwestern.edu'
Subject: [Histonet] slide labeling


Hi,
Just curious because this questions has come up multiple times from 
non-histology people so I thought I'd post it here. When labeling slides at 
microtomy what info do you include on the slide? I know the automated slide 
labelers that are out there will include patient name, surgical number etc.; 
but when handwriting slides as you cut what do you write on them? Currently we 
write the case number, part number and level as well as the cutters initials. 
After staining we put the permanent label on that has patient name and case 
number etc (hence two identifiers). Is there anyone out there who hand writes 
the patient name on the slide or a second identifier on it at the time of 
microtomy?
Thanks for your help,
Lisa

Lisa V.
Chg., IL

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RE: [Histonet] background checks required by AHCA

2011-10-31 Thread Sebree Linda A
Everyone employed in our hospital undergoes periodic background checks. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nicole
Tatum
Sent: Monday, October 31, 2011 9:33 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] background checks required by AHCA

I am currently filing out my ahca renewal application. There are many
changes and the form and I do not find it user friendly. Anyways here my
question: Medical directors and chief finicial officers or any person
who stands to gain profit must undergo a level 2 background screeening.
On the new app is states all empolyees and health care providers. I
called acha licensing division and they said only directors and so
forth. But, on ahca website statue 408(something, ill have to get exact
number) when into effect in 2010 that says all employees and newly hired
employees must underground background screening. So does all the arnp,
pa, ht, and ma's need to be screened because we have a lab?

Nicole Tatum, HT ASCP

http://ahca.myflorida.com/mchq/long_term_care/Background_Screening/BGS_W
hoRequiredToBeScreened.pdf


taken directly from ahca site:

Employees and Contractors employed before August 1, 2010

Every employee/contractor must attest to meeting the requirements of
this chapter and agreeing to inform the employer immediately if arrested
for any of the disqualifying offenses while employed by the employer.
[Section 435.05(2)]. This attestation must be maintained in the
employee's personnel file. You may use the Affidavit of Compliance with
Background Screening to satisfy the attestation requirement.

If an employer becomes aware that an employee/contractor has been
arrested for a disqualifying offense, the employer must remove the
employee/contractor from contact with any vulnerable person that places
the employee/contractor in a role that requires background screening
until the arrest is resolved in a way that the employer determines that
the employee/contractor is still eligible for employment/contracting
under this chapter. [Section 435.06(2)(b)]


Rescreening




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[Histonet] The SC Histo Meeting in Myrtle Beach, SC

2011-10-31 Thread Wanda.Smith
November 4-5, 2011 is the SC Society of Histotechnology meeting at Marina Inn 
at Grande Dunes in Myrtle Beach, SC.  Everyone is still invited even if you 
have not pre-registered!  Gayle Callis is presenting 2 workshops and we 
will have good food and good fellowship  If you think you are coming, 
please email me back so we can get a head count!!!
Thanks,
Wanda

WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC  29406
843-847-4586
843-847-4296 fax


This email and any files transmitted with it may contain PRIVILEGED or 
CONFIDENTIAL information and may be read or used only by the intended 
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[Histonet] Automated coverslipper with Ventana labels

2011-10-31 Thread Theresa (Teri) Johnson
Hi all,

I wanted to ask if any of you out there are currently using an automated 
coverslipper and do not have issues with the forks picking up the slides if 
they have Ventana labels on them.  I have used a Leica and had only very 
occasionally a dropped slide. Is this your experience as well? Are there other 
units that would work well for this?

Feel free to contact me off list if you need to.

Thanks!

Teri Johnson, HT(ASCP)QIHC
GNF Histology Lab Manager
Genomics Institute of the Novartis Research Foundation
858-332-4752

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[Histonet] RE: Automated coverslipper with Ventana labels

2011-10-31 Thread Bea DeBrosse-Serra
Hi Teri, 

And welcome to San Diego  :-)

My experience is, that you cannot leave the slides with the Ventana labels 
sitting in xylene for too long before coverslipping. I believe it is just how 
these labels are and doesn't have much to do with the coverslipper itself.

Bea

Beatrice DeBrosse-Serra HT(ASCP)QIHC
Isis Pharmaceuticals
Antisense Drug Discovery
1896 Rutherford Road
Carlsbad, CA 92008
760-603-2371



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Theresa (Teri) 
Johnson
Sent: Monday, October 31, 2011 10:05 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automated coverslipper with Ventana labels

Hi all,

I wanted to ask if any of you out there are currently using an automated 
coverslipper and do not have issues with the forks picking up the slides if 
they have Ventana labels on them.  I have used a Leica and had only very 
occasionally a dropped slide. Is this your experience as well? Are there other 
units that would work well for this?

Feel free to contact me off list if you need to.

Thanks!

Teri Johnson, HT(ASCP)QIHC
GNF Histology Lab Manager
Genomics Institute of the Novartis Research Foundation
858-332-4752

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[Histonet] Field Histology Tech FL/GA/AL

2011-10-31 Thread Matt Ward
Good Afternoon,



New Position Alert!



Our client is a world leader in Cancer Diagnostics who is currently seeking
Histotechs who have experience working with IHC analyzers that would be
interested in Field Support roles. We currently have an opening covering
Northern FL, AL, and part of GA.







The Position Offers:





- Outstanding Base Salary and Competitive Bonus!







- Gold Standard Benefits including but not limited to Medical, Cell Phone,
Laptop, Car Allowance, Expenses, 401k, Paid Vacation!







- Opportunity for Career Advancement!











If you are interested in learning more please contact me directly at



800.875.6188 ext. 103 or m...@personifysearch.com





Matt Ward

*Account Executive*

*Personify*

5020 Weston Parkway Suite 315

Cary NC 27513

(Tel) 800.875.6188 direct ext 103

(Fax) 919.460.0642

 www.personifysearch.com
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RE: [Histonet] SALARY

2011-10-31 Thread Heath, Nancy L.
Not so good when you fall into a higher tax bracket and uncle sam takes
25% of your salary and the insurance with dental weekly would have cost
me around $232.55 a week...no thanks

 

From: joelle weaver [mailto:joellewea...@hotmail.com] 
Sent: Monday, October 31, 2011 10:35 AM
To: Heath, Nancy L.; jshel...@sanfordburnham.org;
caroline.pr...@uphs.upenn.edu; rcar...@harthosp.org; kcasti...@frii.com;
Histonet
Subject: RE: [Histonet] SALARY

 

I know the cost of living is greater on the east coast, but that sounds
good to me. The insurance is not better, and as an HTL I make less than
1/2 of that! Things are determined by the market I realize, but all
these postings are sure making me feel bad and also realize that I am
not marketing myself well


Joelle Weaver MAOM, BA, (HTL) ASCP
 

 Date: Mon, 31 Oct 2011 06:29:12 -0400
 From: nhe...@lifespan.org
 To: jshel...@sanfordburnham.org; caroline.pr...@uphs.upenn.edu;
rcar...@harthosp.org; kcasti...@frii.com;
Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] SALARY
 CC: 
 
 Just got offered a lead tech position, salary of $85600.00 in a
private lab opened by a group of docs. Didn't take it because the health
insurance plan they offered was lousey. 75% health covered with a 250.00
deductable, dental covered at 60% and no coverage for family or
husbandwould of had to pay that out of pocket.
 I'm in New England.
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of John
Shelley
 Sent: Friday, October 28, 2011 2:25 PM
 To: Pratt, Caroline; Richard Cartun; kcasti...@frii.com;
Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] SALARY
 
 With all that said what are your going rates in this area that you are
speaking.
 
 Kind Regards!
  
 John J Shelley
 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pratt,
Caroline
 Sent: Friday, October 28, 2011 2:19 PM
 To: Richard Cartun; kcasti...@frii.com;
Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] SALARY
 
 If that is an option, I would agree, but non-profit teaching hospitals
 have compensation ranges and grids according to education and
 experience. We keep every employee with the same education and skill
 set at the same compensation for an equitable pay system. If we feel
 our employees are being under paid we will conduct a market analysis
and
 the rates will be increased for all applicable employees if the market
 analysis justifies it.
 
 Car :)
 
 -Original Message-
 From: Richard Cartun [mailto:rcar...@harthosp.org] 
 Sent: Friday, October 28, 2011 12:52 PM
 To: kcasti...@frii.com; Histonet@lists.utsouthwestern.edu; Pratt,
 Caroline
 Subject: RE: [Histonet] SALARY
 
 I think that's low. If you find a good candidate with years of
 experience I would pay them whatever it takes to get them in the door.
 It's like Free Agency in baseball; if you want a good player, you
need
 to put the money on table. Histotechnologists are the most valuable
 employees in the laboratory today! 
 
 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
 
 
  Pratt, Caroline caroline.pr...@uphs.upenn.edu 10/28/2011 9:21
AM
 
 I would say $28 to $32 dollars an hour depending on experience and
 education.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
 kcasti...@frii.com 
 Sent: Friday, October 28, 2011 7:54 AM
 To: Histonet@lists.utsouthwestern.edu 
 Subject: [Histonet] SALARY
 
 HI EVERYONE,
 
 WOULD LIKE TO KNOW WHAT LEAD TECHS AND SUPERVISORS ARE GETTING PAID 
 THESE DAYS. HAVE A FELLOW HISTO PERSON THAT IS RUNNING THEIR OWN DERM 
 LAB AND DOING MOHS ALSO. THANKS FOR YOUR HELP. KRISTY
 
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RE: [Histonet] Alcian blue on the Ventana/Cryoembedding Apparatus

2011-10-31 Thread anita dudley

allison,  we do all of our alcian blue on the machine.  we love it!!
anita dudley
providence hosp
mobile, ala
 

 From: allison_sc...@hchd.tmc.edu
 To: histonet@lists.utsouthwestern.edu
 Date: Fri, 21 Oct 2011 14:00:44 +
 Subject: [Histonet] Alcian blue on the Ventana/Cryoembedding Apparatus
 
 Hello to all in histo land. For those of you that have the ventana special 
 stains machine, can the alcian blue 2.5 be done on the machine? I am not sure 
 if they have kits for this stain. Also is anyone using the cryoembedding 
 apparatus from pathology innovations? Thanks in advance.
 
 Allison Scott HT(ASCP)
 Histology Supervisor
 LBJ Hospital.
 
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[Histonet] RE: Automated coverslipper with Ventana labels

2011-10-31 Thread Burton, Lynn
We have a 15 year old Sakura film coverslipper that has performed famously with 
Venatana labels.
Lynn Burton
Lab Assoc I
Animal Disease Lab
Galesburg, Il
309-344-2451

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Theresa (Teri) Johnson 
[tjohn...@gnf.org]
Sent: Monday, October 31, 2011 12:04 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automated coverslipper with Ventana labels

Hi all,

I wanted to ask if any of you out there are currently using an automated 
coverslipper and do not have issues with the forks picking up the slides if 
they have Ventana labels on them.  I have used a Leica and had only very 
occasionally a dropped slide. Is this your experience as well? Are there other 
units that would work well for this?

Feel free to contact me off list if you need to.

Thanks!

Teri Johnson, HT(ASCP)QIHC
GNF Histology Lab Manager
Genomics Institute of the Novartis Research Foundation
858-332-4752

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