RE: [Histonet] Bachelor's Degrees

2009-12-07 Thread Cynthia Pyse
Tom,
I agree with you about Nate qualifications. Unfortunately in NYS if you
bring in outside work your tech MUST be licensed in NY. The copy of the
license need to be displayed in the lab. I haven't found any way to hire
employees without a license.

Cindy Pyse, CLT, HT (ASCP)
Histology Supervisor
X-Cell Laboratories
e-mail cp...@x-celllab.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Thomas
Jasper
Sent: Saturday, December 05, 2009 3:23 PM
To: Nathan Jentsch
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Bachelor's Degrees

One more reason to consider carefully before throwing support to state
licensure where it does not exist.  I feel sorry for you Nathan and I'd
like to have someone explain the upside of licensing to you.  It seems
it's not about having a license (like a driver's license) to practice
histology.  I fear it's just more about fattening state coffers and
adding another level of bureauracracy to things.

If you are educated (as you are Nate) and if you are academically
eligible to sit for the registry exam.  And if you can satisfactorily
pass the exam, what has state licensing got to do with it?  Are you a
better histologist in New York because you're licensed as opposed to
your neighbors in PA, for example who aren't?  I think not.

Does licensing prove something that science degrees and registry
certifications do not?  Maybe I just don't get it.  And I'm not trying
to pick a fight here with the supporters of licensing.  I just haven't
heard a good convincing argument for it yet.  I'm also quite certain
that even though monetary compensation has improved somewhat, the last
thing most Histologists need is another payment.  The privilege to work
in a certain state, which is paid for (by you) nothing more?!  

I suppose some kindly employers out there somewhere could pay for
it...good luck with that.  Here's an idea, let's say you're degreed and
registry eligible and/or have passed your board exam(s) and are
certified.  How 'bout the state says you've met the qualification for
licensing, here you go!  Nate you are degreed and certified and in my
book and in the book of the current state I live in - Oregon - and the
states I've worked in - Wisconsin, Michigan and Minnesota - you are more
than qualified to work.  I for one would not hesitate in the least to
consider a person such as yourself for employment.  Again you are more
than qualified, even though you are unlicensed. 

I guess I just don't understand how credentialing - degrees and
certifications - aren't enough, but licensing is the magic ticket to
better science/medicine/patient care/whatever.  I'm sure some folks out
there will bring on the firestorm, but again Nathan I feel sorry for you
and I don't see the reasoning behind this.

Tom Jasper

Thomas Jasper HT (ASCP) BAS
Histology Supervisor
Central Oregon Regional Pathology Services
Bend, Oregon 97701
541/693-2677
tjas...@copc.net

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nathan
Jentsch
Sent: Saturday, December 05, 2009 11:46 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Bachelor's Degrees

Paula,
Let me tell you that this is an extremely frustrating point for me not
for getting a job but for getting a license in New York State (which is
related because I'm technically supposed to have a license to work).
Despite the fact that I have a B.S. in a science field and have been
working competently at my job for almost two years now, the state wants
me to have an A.S. in histotechnology to get my license.  They won't
even consider HT certification as sufficient.  If a collective group of
experts in the fields of laboratory science and pathology say I'm
qualified, why isn't that good enough for a bunch of beurocrats who
can't even manage the pocket book of our state.

Nate
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Re: [Histonet] slide handling for special stains

2009-12-07 Thread V. Neubert
I don't see any point in leaving deparaffinized and rehydrated(!) slides 
any longer in water. The tissue might even fall off.


What special stains are you goint to do?



Hello all,
I need some information on special stains in regards to handling of slides.   
Would it be good practice to deparaffinize and rehydrate slides then allow them 
to sit in water over night or over the weekend before doing the actual staining?
Thanks
Roger

Roger Charles
Microbiologist
Pennsylvania Veterinary Laboratory
2305 N Cameron St
Harrisburg, PA 17110
717-787-8808
rchar...@state.pa.usmailto:rchar...@state.pa.us


No trees were hurt in the sending of this email, However many electrons were 
severely inconvenienced!

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Re: [Histonet] slide handling for special stains

2009-12-07 Thread Kim . Donadio
I wouldn't make that a habit. It eventually saturates the cells and then 
they fall off like the previous poster mentioned. Also, especially leaving 
them in water for a whole weekend you risk contamination. Not good 
practice. If you absolutely have to leave them in something after they 
have been deparaffinized I would suggest 95% alcohol. With that said, I 
think best practice would be to leave them paraffinized until you have 
time to do the stains. 




Kim Donadio 
Pathology Supervisor
Baptist Hospital
1000 W Moreno St.
Pensacola FL 32501
Phone (850) 469-7718
Fax (850) 434-4996



Charles, Roger rchar...@state.pa.us 
Sent by: histonet-boun...@lists.utsouthwestern.edu
12/07/2009 07:19 AM

To
Histonet (histonet@lists.utsouthwestern.edu) 
histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] slide handling for special stains






Hello all,
I need some information on special stains in regards to handling of 
slides.   Would it be good practice to deparaffinize and rehydrate slides 
then allow them to sit in water over night or over the weekend before 
doing the actual staining?
Thanks
Roger

Roger Charles
Microbiologist
Pennsylvania Veterinary Laboratory
2305 N Cameron St
Harrisburg, PA 17110
717-787-8808
rchar...@state.pa.usmailto:rchar...@state.pa.us


No trees were hurt in the sending of this email, However many electrons 
were severely inconvenienced!

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RE: [Histonet] Bachelor's Degrees

2009-12-07 Thread Rene J Buesa
Cindy:
And not being able to hire anybody without the license is absolutely great and 
why the license was created in the firs place, namely, to avoid having low paid 
people doing histology work in detriment to others more qualified.
The salary competition posed by those not licensed is the cause for the low pay 
histotechs receive when compared with other professionals in the medical 
laboratory.
That was exactly the point: to assure a just salary for histotechs.
René J.

 

--- On Mon, 12/7/09, Cynthia Pyse cp...@x-celllab.com wrote:


From: Cynthia Pyse cp...@x-celllab.com
Subject: RE: [Histonet] Bachelor's Degrees
To: 'Thomas Jasper' tjas...@copc.net, 'Nathan Jentsch' 
njblademas...@gmail.com
Cc: histonet@lists.utsouthwestern.edu
Date: Monday, December 7, 2009, 8:12 AM


Tom,
I agree with you about Nate qualifications. Unfortunately in NYS if you
bring in outside work your tech MUST be licensed in NY. The copy of the
license need to be displayed in the lab. I haven't found any way to hire
employees without a license.

Cindy Pyse, CLT, HT (ASCP)
Histology Supervisor
X-Cell Laboratories
e-mail cp...@x-celllab.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Thomas
Jasper
Sent: Saturday, December 05, 2009 3:23 PM
To: Nathan Jentsch
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Bachelor's Degrees

One more reason to consider carefully before throwing support to state
licensure where it does not exist.  I feel sorry for you Nathan and I'd
like to have someone explain the upside of licensing to you.  It seems
it's not about having a license (like a driver's license) to practice
histology.  I fear it's just more about fattening state coffers and
adding another level of bureauracracy to things.

If you are educated (as you are Nate) and if you are academically
eligible to sit for the registry exam.  And if you can satisfactorily
pass the exam, what has state licensing got to do with it?  Are you a
better histologist in New York because you're licensed as opposed to
your neighbors in PA, for example who aren't?  I think not.

Does licensing prove something that science degrees and registry
certifications do not?  Maybe I just don't get it.  And I'm not trying
to pick a fight here with the supporters of licensing.  I just haven't
heard a good convincing argument for it yet.  I'm also quite certain
that even though monetary compensation has improved somewhat, the last
thing most Histologists need is another payment.  The privilege to work
in a certain state, which is paid for (by you) nothing more?!  

I suppose some kindly employers out there somewhere could pay for
it...good luck with that.  Here's an idea, let's say you're degreed and
registry eligible and/or have passed your board exam(s) and are
certified.  How 'bout the state says you've met the qualification for
licensing, here you go!  Nate you are degreed and certified and in my
book and in the book of the current state I live in - Oregon - and the
states I've worked in - Wisconsin, Michigan and Minnesota - you are more
than qualified to work.  I for one would not hesitate in the least to
consider a person such as yourself for employment.  Again you are more
than qualified, even though you are unlicensed. 

I guess I just don't understand how credentialing - degrees and
certifications - aren't enough, but licensing is the magic ticket to
better science/medicine/patient care/whatever.  I'm sure some folks out
there will bring on the firestorm, but again Nathan I feel sorry for you
and I don't see the reasoning behind this.

Tom Jasper

Thomas Jasper HT (ASCP) BAS
Histology Supervisor
Central Oregon Regional Pathology Services
Bend, Oregon 97701
541/693-2677
tjas...@copc.net

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nathan
Jentsch
Sent: Saturday, December 05, 2009 11:46 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Bachelor's Degrees

Paula,
Let me tell you that this is an extremely frustrating point for me not
for getting a job but for getting a license in New York State (which is
related because I'm technically supposed to have a license to work).
Despite the fact that I have a B.S. in a science field and have been
working competently at my job for almost two years now, the state wants
me to have an A.S. in histotechnology to get my license.  They won't
even consider HT certification as sufficient.  If a collective group of
experts in the fields of laboratory science and pathology say I'm
qualified, why isn't that good enough for a bunch of beurocrats who
can't even manage the pocket book of our state.

Nate
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Re: [Histonet] slide handling for special stains

2009-12-07 Thread Rene J Buesa
No, it is not a good idea. In many occasions leaving the dewaxed sections in DW 
for prolonged periods of time can cause the section to peel off (not always, 
but sometimes).
The idea is to dewax and do the special stains immediately after.
René J.

--- On Mon, 12/7/09, Charles, Roger rchar...@state.pa.us wrote:


From: Charles, Roger rchar...@state.pa.us
Subject: [Histonet] slide handling for special stains
To: Histonet (histonet@lists.utsouthwestern.edu) 
histonet@lists.utsouthwestern.edu
Date: Monday, December 7, 2009, 8:19 AM


Hello all,
I need some information on special stains in regards to handling of 
slides.   Would it be good practice to deparaffinize and rehydrate slides then 
allow them to sit in water over night or over the weekend before doing the 
actual staining?
Thanks
Roger

Roger Charles
Microbiologist
Pennsylvania Veterinary Laboratory
2305 N Cameron St
Harrisburg, PA 17110
717-787-8808
rchar...@state.pa.usmailto:rchar...@state.pa.us


No trees were hurt in the sending of this email, However many electrons were 
severely inconvenienced!

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[Histonet] opinion please

2009-12-07 Thread Kim Merriam
Help!

My refrigerator died over the weekend.  This fridge had most of my antibodies 
and IHC reagents.  When I came in, the temperature inside the fridge was a 
balmy 37C!

Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA 



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[Histonet] CM 3600

2009-12-07 Thread Terry OBrien
Looking for someone close to Pittsburgh, PA (or within a 300 miles) with a
Leica CM3600 that I could come by and look at.

Thanks,
Terry
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Re: [Histonet] opinion please

2009-12-07 Thread Kim . Donadio
Amazing! How hot do you keep the room temp there? 

I would toss them, one false test on a patient is more valuable than all 
those lost reagents. 




Kim Donadio 
Pathology Supervisor
Baptist Hospital
1000 W Moreno St.
Pensacola FL 32501
Phone (850) 469-7718
Fax (850) 434-4996



Kim Merriam kmerriam2...@yahoo.com 
Sent by: histonet-boun...@lists.utsouthwestern.edu
12/07/2009 08:51 AM

To
Histonet histonet@lists.utsouthwestern.edu
cc

Subject
[Histonet] opinion please






Help!

My refrigerator died over the weekend.  This fridge had most of my 
antibodies and IHC reagents.  When I came in, the temperature inside the 
fridge was a balmy 37C!

Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA 


 
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Re: [Histonet] opinion please

2009-12-07 Thread Rene J Buesa
Perhaps yes or perhaps no, that is the problem.
From now on you cannot know if something that did not work was because of the 
fridge malfunction.
Advise? (Costly advise?): discard everything and get an alarm system for your 
fridge after you repair it (or get a new one)..
René J.

--- On Mon, 12/7/09, Kim Merriam kmerriam2...@yahoo.com wrote:


From: Kim Merriam kmerriam2...@yahoo.com
Subject: [Histonet] opinion please
To: Histonet histonet@lists.utsouthwestern.edu
Date: Monday, December 7, 2009, 9:51 AM


Help!

My refrigerator died over the weekend.  This fridge had most of my antibodies 
and IHC reagents.  When I came in, the temperature inside the fridge was a 
balmy 37C!

Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA 



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Re: [Histonet] opinion please

2009-12-07 Thread Greg Dobbin
I agree with Renee. It will proabaly be at least as costly to have to 
re-validate everything!
Greg

Greg Dobbin, R.T.
Chief Technologist, Anatomic Pathology
Dept. of Laboratory Medicine,
Queen Elizabeth Hospital,
P.O. Box 6600
Charlottetown, PEC1A 8T5
Phone: (902) 894-2337
Fax: (902) 894-2385

I find that the harder I work, the 
more luck I seem to have.
- Thomas Jefferson


 Rene J Buesa rjbu...@yahoo.com 12/7/2009 11:21 AM 
Perhaps yes or perhaps no, that is the problem.
From now on you cannot know if something that did not work was because of the 
fridge malfunction.
Advise? (Costly advise?): discard everything and get an alarm system for your 
fridge after you repair it (or get a new one)..
René J.

--- On Mon, 12/7/09, Kim Merriam kmerriam2...@yahoo.com wrote:


From: Kim Merriam kmerriam2...@yahoo.com
Subject: [Histonet] opinion please
To: Histonet histonet@lists.utsouthwestern.edu
Date: Monday, December 7, 2009, 9:51 AM


Help!

My refrigerator died over the weekend.  This fridge had most of my antibodies 
and IHC reagents.  When I came in, the temperature inside the fridge was a 
balmy 37C!

Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA 



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[Histonet] FW: OT fuchsia

2009-12-07 Thread Johnson, Teri
 
One of the researchers here summed it up nicely when he reported that most 
discoveries in the lab are not heralded with cries of Eureka!, but rather 
with hmmmnow that's interesting...

Teri Johnson, HT(ASCP)QIHC
Stowers Institute for Medical Research
Kansas City, MO
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[Histonet] Glypican 3

2009-12-07 Thread Rick . Garnhart

Anyone out there know were Glypican 3 antibody for IHC may be purchased from.


Rick Garnhart HT(ASCP)
Memorial Health System
Histology Supervisor
1400 E. Boulder St.
Colorado Springs, CO 80909
Cell: 719-365-8357
Ph:  719-365-6926
Fax: 719-365-6373
rick.garnh...@memorialhealthsystem.com



Mission: To provide the highest quality health care
Vision: To create an outstanding health system where patients heal and people 
thrive
Values: Compassion - Integrity - Quality - Respect - Teamwork

www.memorialhealthsystem.com

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Re: [Histonet] Overstaining - Mayers HE

2009-12-07 Thread Rene J Buesa
You have to consider that the thicker the section the more intense the staining 
will be.
If you are using now 1 minute and they are still too dark, reduce the staining 
time even further.
Otherwise I don't see anything wrong with the rest of the protocol.
René J.

--- On Mon, 12/7/09, Josephine Garcia j...@u.washington.edu wrote:


From: Josephine Garcia j...@u.washington.edu
Subject: [Histonet] Overstaining - Mayers HE
To: histonet@lists.utsouthwestern.edu
Date: Monday, December 7, 2009, 11:42 AM


Hi all,

My (frozen-section, fixed) slides are coming out much too dark (overstained
purple) and I'm not sure why. They are 15-20 micrometer slices of rat
gastrocnemius muscle. Can someone please look over our current protocol and
tell me what I'm doing wrong? Thanks! Here it is:

1. Perfuse animal with 4% paraformaldehyde fixative.
2. Soak in 0.4% paraformaldehyde
3. Sucrose cycle (5% rinse, 10%, 20%, 30% soak)
4. Embed in OCT, Frozen sections (15-20 micrometers)
5. Let dry for 15-30 min
6. Stain as follows:

- Distilled H2O (quick dip)
- Mayer's Hematoxylin - 1min (originally we were dipping for 5-10 minutes. I
slowly reduced the time to 2min, then 1min, then 30s... still overstained!)
- Running lukewarm tap water - drain and continuously fill - 15min or until
water runs clear
- Distilled H2O (quick dip)
- 80% EtOH - 1-2min
- Eosin - 2 min
- 95% EtOH I - 10sec
- 95% EtOH  II - 10sec
- 100% EtOH I - 10sec
- 100% EtOH II - 10sec
- Xylene I - 2min
- Xylene II - 2min

7. Coverslip and let dry overnight
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[Histonet] FW: Coarse abrasive

2009-12-07 Thread Hannen, Valerie
 



From: Hannen, Valerie 
Sent: Friday, December 04, 2009 9:43 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Coarse abrasive


Help!! My section chief just got word that Leica is no longer producing
coarse abrasive. We only have steel blades in our department and we are
SO dependent on the abrasives. She does not want to  switch to
disposable blades. Is there anyone out there in Histo-land who might
know a solution to our dilema.
 
Thanks in advance for your answers.
 
Valerie Hannen,MLT(ASCP),HTL,SU(FL)
Parrish Medical Center
951 N. Washington Ave.
Titusville, Florida 32796


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Re: [Histonet] FW: Coarse abrasive

2009-12-07 Thread Jan . Minshew
Hello Valerie,

I believe you may have been given misinformation regarding the knife
sharpening abrasives.  You can order through Leica Microsystems using
catalog number 14041819700 for a single bottle or 14937000 for a case of 6
bottles.

Please feel free to contact me if you have any questions.

Best wishes,


Jan Minshew, HT/HTL(ASCP)
Marketing Manager
Leica Microsystems
Biosystems Division
2345 Waukegan Road
Bannockburn, IL 60015

800.248.0123 Toll Free
847.405.7051 Direct
847.405.6560 Fax

www.leica-microsystems.com

Click Here for this month's special offers!


   
 Hannen, Valerie 
 valerie.han...@p 
 arrishmed.com To 
 Sent by:  histonet@lists.utsouthwestern.edu 
 histonet-bounces@  cc 
 lists.utsouthwest 
 ern.edu   Subject 
   [Histonet] FW: Coarse abrasive  
   
 12/07/2009 12:01  
 PM
   
   
   








From: Hannen, Valerie
Sent: Friday, December 04, 2009 9:43 AM
To: 'histo...@list.utsouthwestern.edu'
Subject: Coarse abrasive


Help!! My section chief just got word that Leica is no longer producing
coarse abrasive. We only have steel blades in our department and we are
SO dependent on the abrasives. She does not want to  switch to
disposable blades. Is there anyone out there in Histo-land who might
know a solution to our dilema.

Thanks in advance for your answers.

Valerie Hannen,MLT(ASCP),HTL,SU(FL)
Parrish Medical Center
951 N. Washington Ave.
Titusville, Florida 32796


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Re: [Histonet] Overstaining - Mayers HE

2009-12-07 Thread Bryan Llewellyn

There doesn't appear to be anything wrong with the staining schedule.

Mayer published more than one alum hematoxylin and one of them is a strong 
regressive type, and would produce the staining you see.  Is it possible 
that has been used instead of his progressive one?  If it has, make the 
following diluent.


Potassium or ammonium alum 50 g
Citric acid 1 g or glacial acetic acid 20 mL
Distilled water 1L

Then dilute the strong alum hematoxylin 1 part with 3 parts diluent.

Or,

Immediately before the 80% ethanol prior to the eosin, place into a solution 
of 0.5% acid ethanol for a few seconds.  Wash well to blue, and carry on.


If that doesn't correct it, then make up a fresh batch of Mayer's hemalum.

Bryan Llewellyn



- Original Message - 
From: Josephine Garcia j...@u.washington.edu

To: histonet@lists.utsouthwestern.edu
Sent: Monday, December 07, 2009 8:42 AM
Subject: [Histonet] Overstaining - Mayers HE



Hi all,

My (frozen-section, fixed) slides are coming out much too dark 
(overstained

purple) and I'm not sure why. They are 15-20 micrometer slices of rat
gastrocnemius muscle. Can someone please look over our current protocol 
and

tell me what I'm doing wrong? Thanks! Here it is:

1. Perfuse animal with 4% paraformaldehyde fixative.
2. Soak in 0.4% paraformaldehyde
3. Sucrose cycle (5% rinse, 10%, 20%, 30% soak)
4. Embed in OCT, Frozen sections (15-20 micrometers)
5. Let dry for 15-30 min
6. Stain as follows:

- Distilled H2O (quick dip)
- Mayer's Hematoxylin - 1min (originally we were dipping for 5-10 minutes. 
I
slowly reduced the time to 2min, then 1min, then 30s... still 
overstained!)
- Running lukewarm tap water - drain and continuously fill - 15min or 
until

water runs clear
- Distilled H2O (quick dip)
- 80% EtOH - 1-2min
- Eosin - 2 min
- 95% EtOH I - 10sec
- 95% EtOH  II - 10sec
- 100% EtOH I - 10sec
- 100% EtOH II - 10sec
- Xylene I - 2min
- Xylene II - 2min

7. Coverslip and let dry overnight
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RE: [Histonet] FL Supervisor License

2009-12-07 Thread Santiago, Jerry
Marie,

If the person is licensed as a technologist with no ASCP certification
but at least 5 years of experience, he/she qualifies under rule
64B3-5.002(C)(3). See below.


64B3-5.002 Supervisor.
Qualifications and Responsibilities.
(1) Qualification. Degrees or semester hours of academic credit required
in this section shall be obtained at a regionally accredited college or
university or by foreign education equated pursuant to subsection
64B3-6.002(6), F.A.C. In order to be licensed as a supervisor, an
applicant shall be licensed or meet the requirements for licensure as a
technologist, have a Board approved 2-hour course relating to the
prevention of medical errors, which shall include root-cause analysis,
error reduction and prevention, patient safety, complete an educational
course acceptable to the Department on human immunodeficiency virus and
acquired immune deficiency syndrome, and one of the following:

(c) Histology

Route 1

Five years of pertinent clinical laboratory experience in histology and
25 hours of Board-approved continuing education in supervision and
administration within the previous 5 years and HTL (ASCP)

Route 2

Five years of pertinent clinical laboratory experience
post-certification and 48 hours of Board-approved continuing education
in supervision and administration within the previous 5 years and HT
(ASCP)

Route 3

Five years of pertinent clinical laboratory experience, and 48 hours of
Board-approved continuing education in supervision and administration
within the previous 5 years, and licensure as a technologist in the
specialty of histology

Jerry Santiago, BS, HTL(ASCP)QIHC
Shands Jacksonville
655 W 8th Street
Jacksonville, FL  32209
Tel: 904-244-6149
E-mail: jerry.santi...@jax.ufl.edu




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
histospr...@aol.com
Sent: Wednesday, December 02, 2009 1:00 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] FL Supervisor License


This may have been covered already, please accept my apologies for a
repeat question. I was curious if anyone knows if you can upgrade a
technologist (FL state license only, grandfathered in so NO ASCP)
license WITHOUT a 4 year degree? The work experience is 10+ years but
this person does NOT have a 2 or 4 year degree of any kind. I know the
laws constantly change, was just curious about the current ones, I am
not familiar with ASCP guidelines for FL. 
Thank you in advance.
Marie
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RE: [Histonet] opinion please

2009-12-07 Thread Morken, Tim
Kim,

Test a random sampling (10%) of the antibodies and see if they work. If so, 
then they are most likely fine. Document the test. Antibodies are very robust 
and the warmup probably won't damage many, if any, of them. 

BTW, When I worked for an antibody manufacturer I did a test once as part of a 
stability problem investigation and left six different antibodies in a 37C oven 
for up to 4 months. We tested a sample of each weekly. All worked fine and some 
even worked better even after 4 months!

The issue I would be concerned about is bacterial growth in any of them. Keep 
an eye on that.

Tim Morken
Supervisor, Histology / IPOX
UCSF Medical Center
San Francisco, CA  
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Kim Merriam
Sent: Monday, December 07, 2009 6:51 AM
To: Histonet
Subject: [Histonet] opinion please

Help!

My refrigerator died over the weekend.  This fridge had most of my antibodies 
and IHC reagents.  When I came in, the temperature inside the fridge was a 
balmy 37C!

Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA 


  
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[Histonet] plasminogen activator inhibitor 1 (PAI 1) antibody

2009-12-07 Thread Walters, Katherine S
Has anyone had any experience with this antibody?  There are many
companies selling them and I'm not sure which would be best for my
paraffin-embedded human tissue?

Katherine Walters
Histology Director
Central Microscopy Research Facilities
85 Eckstein Medical Research Building
University of Iowa
Iowa City, Iowa 52242-1101

phone: # 319-335-8142
fax:  # 319-384-4469

katherine-walt...@uiowa.edu
www.uiowa.edu/~cemrf




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Re: [Histonet] opinion please

2009-12-07 Thread Akemi Allison


I agree with Tim.  This is a very common practice for antibody  
manufacturer's.   Also, manufacturer's will revalidate antibodies  
when they are close to their exploration date and if that antibody  
has the same sensitivity.  They will extend the shelf-life date.


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

On Dec 7, 2009, at 2:32 PM, Morken, Tim wrote:


Kim,

Test a random sampling (10%) of the antibodies and see if they  
work. If so, then they are most likely fine. Document the test.  
Antibodies are very robust and the warmup probably won't damage  
many, if any, of them.


BTW, When I worked for an antibody manufacturer I did a test once  
as part of a stability problem investigation and left six different  
antibodies in a 37C oven for up to 4 months. We tested a sample of  
each weekly. All worked fine and some even worked better even after  
4 months!


The issue I would be concerned about is bacterial growth in any of  
them. Keep an eye on that.


Tim Morken
Supervisor, Histology / IPOX
UCSF Medical Center
San Francisco, CA


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet- 
boun...@lists.utsouthwestern.edu] On Behalf Of Kim Merriam

Sent: Monday, December 07, 2009 6:51 AM
To: Histonet
Subject: [Histonet] opinion please

Help!

My refrigerator died over the weekend.  This fridge had most of my  
antibodies and IHC reagents.  When I came in, the temperature  
inside the fridge was a balmy 37C!


Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA



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Re: [Histonet] opinion please

2009-12-07 Thread Akemi Allison
Sorry I made a type O I meant to say Also, manufacturer's will  
revalidate antibodies when they are close to their expiration date  
and if that antibody has the same sensitivity.  They will extend the  
shelf-life date.





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

On Dec 7, 2009, at 5:02 PM, Akemi Allison wrote:



I agree with Tim.  This is a very common practice for antibody  
manufacturer's.   Also, manufacturer's will revalidate antibodies  
when they are close to their exploration date and if that antibody  
has the same sensitivity.  They will extend the shelf-life date.


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

On Dec 7, 2009, at 2:32 PM, Morken, Tim wrote:


Kim,

Test a random sampling (10%) of the antibodies and see if they  
work. If so, then they are most likely fine. Document the test.  
Antibodies are very robust and the warmup probably won't damage  
many, if any, of them.


BTW, When I worked for an antibody manufacturer I did a test once  
as part of a stability problem investigation and left six  
different antibodies in a 37C oven for up to 4 months. We tested a  
sample of each weekly. All worked fine and some even worked better  
even after 4 months!


The issue I would be concerned about is bacterial growth in any of  
them. Keep an eye on that.


Tim Morken
Supervisor, Histology / IPOX
UCSF Medical Center
San Francisco, CA


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet- 
boun...@lists.utsouthwestern.edu] On Behalf Of Kim Merriam

Sent: Monday, December 07, 2009 6:51 AM
To: Histonet
Subject: [Histonet] opinion please

Help!

My refrigerator died over the weekend.  This fridge had most of my  
antibodies and IHC reagents.  When I came in, the temperature  
inside the fridge was a balmy 37C!


Do you think any of my reagents are still usable?

Kim
 Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA



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[Histonet] Mircom 505 E Cryostat 0000

2009-12-07 Thread Karen Young
Hi,

 We have a microm 505 E cryostat in the lab, the microtome part of which
a repairer came to clean. Since the return of the microtome to the
cryostat, when we turn it on we no longer get any of the error messages
specified in the manual (such as those that come up when the cryostat
has been off for a while and is not cool), but rather the displays show
. The blank reset button does not work and nor do any of the other
buttons.  I can find no reference to this display in our manual. Does
anyone know what  means or how it can be fixed?

 

Many Thanks,

 

Karen.

PhD Candidate

School of Biological Sciences

University of Queensland

Goddard Building (8), Rm 363a

 

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Re: [Histonet] opinion please

2009-12-07 Thread Bader Siddiki
Hello
I have the same experience.
When I worked for a company and right after 9/11, we shipped antibodies to
Israel via Post office at ambient temp.
This package came back after 6-8 weeks or may be longer.
We do not know how they were stored at post office.
We tested the antibodies and could not find differences in the activity
using IHC.
Bader

On Mon, Dec 7, 2009 at 4:02 PM, Akemi Allison akemiat3...@yahoo.com wrote:


 I agree with Tim.  This is a very common practice for antibody
 manufacturer's.   Also, manufacturer's will revalidate antibodies when they
 are close to their exploration date and if that antibody has the same
 sensitivity.  They will extend the shelf-life date.

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

 On Dec 7, 2009, at 2:32 PM, Morken, Tim wrote:

  Kim,

 Test a random sampling (10%) of the antibodies and see if they work. If
 so, then they are most likely fine. Document the test. Antibodies are very
 robust and the warmup probably won't damage many, if any, of them.

 BTW, When I worked for an antibody manufacturer I did a test once as part
 of a stability problem investigation and left six different antibodies in a
 37C oven for up to 4 months. We tested a sample of each weekly. All worked
 fine and some even worked better even after 4 months!

 The issue I would be concerned about is bacterial growth in any of them.
 Keep an eye on that.

 Tim Morken
 Supervisor, Histology / IPOX
 UCSF Medical Center
 San Francisco, CA


 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet-
 boun...@lists.utsouthwestern.edu] On Behalf Of Kim Merriam
 Sent: Monday, December 07, 2009 6:51 AM
 To: Histonet
 Subject: [Histonet] opinion please

 Help!

 My refrigerator died over the weekend.  This fridge had most of my
 antibodies and IHC reagents.  When I came in, the temperature inside the
 fridge was a balmy 37C!

 Do you think any of my reagents are still usable?

 Kim
  Kim Merriam, MA, HT(ASCP)QIHC
 Cambridge, MA



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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.
Phone: + 425 367 4601
Phone: + 425 514 3761
Fax: + 425 367 4817
cell (mobile) phone: + 425 314 0199
e-mail address: bade...@gmail.com
Web site: www.immunobioscience.com
Marketing: phone: + 650 343 IBSC (4272)
   E-mail: anitai...@aol.com
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[Histonet] re: bachelor's degrees

2009-12-07 Thread Nathan Jentsch
Rene makes an excellent point as to the reason for having a license.  I
agree that it is a good idea.  Unfortunately NYS took the idea and botched
it.  The NSH tried to push them in the direction of using the HT exam as
their qualifying exam, but instead they want to write their own and they are
placing unrealistic education requirements.  There is only one school in NYS
to get an A.S. in histotechnology, and it would require most people in the
state to relocate well away from where they have established their careers.
I don't think the bureaucrats realize that they are making it difficult for
labs to fill positions, and this will only get worse as people retire from
the field and there will only be a handful of fresh graduates every year.
As it stands now, I will be taking an online program through Indiana
University starting in August in order to meet the requirements set for me.
Hopefully they will grant me a limited license until I finish the program so
that I can continue to work.
Nathan Jentsch
B.S. Environmental Science
Rochester Institute of Technology
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pH meter calibration. Was Re: [Histonet] Alcian Blue

2009-12-07 Thread John Kiernan
A pH meter must be calibrated hourly or daily, not monthly! 
 
In a research environment, with frequently changing chemicals that might damage 
the glass electrode, you need to calibrate against standard (usually bought) 
buffers several times within every day. pH meter electrodes are horribly 
fragile and horribly expensive. Replacing them is a big item in every lab's 
budget. 
 
John Kiernan
Anatomy, UWO
London, Canada
= = =
- Original Message -
From: Diana McCaig dmcc...@ckha.on.ca
Date: Sunday, December 6, 2009 13:49
Subject: [Histonet] Alcian Blue
To: histonet@lists.utsouthwestern.edu

 In the past, when we made up 1% Alcian blue in 3% acetic acid (using
 bottle distilled water), the pH was always 2.5.  We did not 
 have to
 modify it to get the proper pH.  Still using the same 
 powder, we are
 getting a pH of 2.1.  I hate to adjust it because it seems 
 to affect the
 staining.  Any suggestions.  The pH meter is 
 calibrated monthly.
  
 Diana 
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[Histonet] paper on osteoclasts

2009-12-07 Thread louise renton
Hi all,

I am going crazy - and its not even friday yet! A little while ago (OK about
3 years) i came across a paper where the researcher had shown the transition
of macrophages to osteoclasts  using immuno staining - i cannot seem to find
it on Pubmed, dont know the author date or journal.

i hope soemone out there can help

best egards

-- 
Louise Renton
Bone Research Unit
University of the Witwatersrand
Johannesburg
South Africa
There are nights when the wolves are silent and only the moon howls.
George Carlin
No trees were killed in the sending of this message.
However, many electrons were terribly inconvenienced.
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