Re: [Histonet] Bodian

2013-10-04 Thread LuAnn Anderson
Renecould I please get a copy of that procedure ?  I would 
greatly appreciate it.


On 10/4/2013 9:35 AM, Rene J Buesa wrote:

The fundamental problem with the Bodian stain is the silver protargol. Once you 
open your expensive bottle (only very few manufacturers of the powder) it 
starts to oxidize end in only a few days it is no longer able to react properly.
That is why I developed a procedure where you prepare your own silver protargol 
FRESH before every procedure. This, although sound difficult, it is not. Under 
separate cover I am sending you a publication I did on this method and I am 
sure you will overcome all your difficulties.
René J.

  



From: Helene Degan deg...@upstate.edu
To: histonet@lists.utsouthwestern.edu
Sent: Thursday, October 3, 2013 4:38 PM
Subject: [Histonet] Bodian


Hi
Thanks to every one that sent me Acid Phosphotase procedure for muscle 
biopsies. I also need some help with the bodian stain, we are not  getting any 
staining on the slides, we have a procedure that they used years ago and now we 
can't get it working (we did purchase new chemicals) and we also tried a stain 
kit with very little results.

Thanks again

Helene
Upstate Medical University

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Re: [Histonet] Farewell

2012-03-30 Thread LuAnn Anderson
   Wishing you all the best in your retirement, Sally !! Do try to keep 
in touch though~~your advice and expertise will be missed !!!  Enjoy!


LuAnn



On 3/30/2012 8:41 AM, Rene J Buesa wrote:

Sarah:
It has been always a pleasure communicating with you as we have done so many 
times in the past.  You are a real specialist in the difficult field of 
veterinary histology and you should remember that when in retirement.
Try to pass on your knowledge. Being retired does not mean to go into mental 
hibernation.
Participate in HistoNet even more than before. Now you are the owner of your 
time.
My sincere congratulations and enjoy your retirement as I have been doing for 
the last 10 years.
René J.

--- On Fri, 3/30/12, Breeden, Sarasbree...@nmda.nmsu.edu  wrote:


From: Breeden, Sarasbree...@nmda.nmsu.edu
Subject: [Histonet] Farewell
To: histonet@lists.utsouthwestern.edu
Date: Friday, March 30, 2012, 9:16 AM


Hard as it is to believe - and I probably won't until I've been away for
a week or more - this is my LAST day to work.  Retirement? Who knew it
would come around so fast? I remember having only fifteen years left to
work and that was just yesterday!  Histology has been 'bery, 'bery good
to me and although I fell into it by accident, it has been a
fascinating, involving, liberating experience.  I'll be lurking on
Histonet but under the alias of nmhisto and I'll probably do some p.r.n.
work but I'm going home and throwing away my alarm clock and resetting
the coffee maker for 6:00 a.m. instead of 3:45 a.m.  Thank you all for
your advice, guidance, humor, relative insanity and wisdom.  Enjoy what
you do and try to recruit at least one person into this field before
it's your time to pick out the color of the tennis balls on your walker.



Hail and Farewell and best of everything to every one of you.



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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Re: [Histonet] Re[2]:

2012-03-27 Thread LuAnn Anderson
I agree~~they need to be deleted from Histonet !!  Getting them several 
times daily !



On 3/27/2012 12:05 PM, Kara Lee wrote:

I am getting these constantly as well.  Very annoying.


Date: Tue, 27 Mar 2012 11:58:39 -0500
From: jmitch...@uwhealth.org
To: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re[2]:

How about these postings to histonet?  Is everyone else getting these
from Tuyen Nguyen  Diamond Ranch Music?  If so - can these people/email
addresses be deleted from the histonet service?

A little redneck humor is one thing - but the love boutique sex shop is
another.

Jean Mitchell

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tuyen
Nguyen
Sent: Tuesday, March 27, 2012 11:23 AM
To: histonet@lists.utsouthwestern.edu; boost...@diamondranchmusic.org
Subject: [Histonet] Re[2]:


Welcome, friend!
http://loveboutiquesexshop.com/contact.php?yfupu=65ugazylycy=167myroli
ma=28

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Re: [Histonet] PAS staining

2010-10-06 Thread LuAnn Anderson
 I still make my own Schiff's reagent. It is easy to make and I've 
never had a problem with it. Keeps well in refrigerator. I do make the 
periodic acid fresh each time. If anyone wants the recipe, let me know.


LuAnn


On 10/6/2010 11:43 AM, Janet Keeping wrote:

I have for some time had a problem with Schiff's reagent and PAS staining.

- I have tested each new, unopened bottle of Schiff's reagent with
formaldehyde and always the color development was immediate, but purple,
definately not pink.This result has been quite consistant.
- PAS staining for glycogen using the method in *Histotechnology a self
Instructional text,* would fail to demonstrate any glycogen in autopsy
liver specimens.

I teach Histology at a community college and this problem has driven me
crazy for a number of years. I have tried several brands of Schiff with the
same results. Recently I obtained sheep tissues which were promptly
refrigerated and fixed after death, and I had hoped these tissues would
demonstrate glycogen. ( My thinking was that perhaps delay before autopsy
was somehow diminishing the glycogen in the specimens that I had.or that
perhaps long term NBF fixation had hampered staining.) Basement membranes
were stained with the Schiff reagent as expected despite the purple color in
the formaldehyde test. Hotchkiss Mcmanus with the same reagent also produced
beautiful staining of fungus a lovely magenta color. A search of the web
made me suspiciious when I noted that Schiff added to 37-40% formaldehyde
should produce a pink or red color, however, A spot check of formalin using
Schiff should produce a purple color. I sent an e-mail to Brian Hewlett to
ask if he could make any recommendation.

Brian was not surprised by the purple color devopment in testing, He
suggested that a large number of available aldehyde groups would be expected
to produce this color. He suggested that I increase my periodate oxidation
to 20-30 minutes and my Schiff application to 30 minutes.

This worked and I am extremely grateful!. Has anyone else had an experience
like this?
Janet
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[Histonet] histology stories

2010-03-11 Thread LuAnn Anderson

Another funny story:
 When my son was in kindergarten, the teacher went around the class 
asking the kids what their parents did. When she got to Michael he 
stood up and announced quite boldly she cuts up brains!!. The 
teacher asked me at the next conference what I really did and after 
explaining histology to her, she told me the story and said that she 
was afraid to ask him for more details on that day!  I got a chuckle 
out of that and so did she!


LuAnn 
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Re: [Histonet] Victoria Blue stain

2009-11-04 Thread LuAnn Anderson


VICTORIA BLUE - NUCLEAR FAST RED FOR HBSAg

PRINCIPLE
To demonstrate copper associated protein, elastic 
and Hepatitis B surface antigen (HBSAg) in paraffin wax sections.


REFERENCE
. AFIP laboratory methods in Histotechnology p210 
Tanaka method Ref:Acta Pathol Jpn 1981;31:93


SPECIMEN
10% neutral buffered formalin. Standard paraffin wax sections.

CONTROL
Known case of primary biliary cirrhosis.

REAGENTS
(A) VICTORIA BLUE
Distilled water 200 mL Dextrine 0.5 g Victoria 
Blue 2 g Resorcinol 4 g Gradually warm up the 
mixed solution of all the above until it boils. 
Remove form heat then gradually add 25mL of 
boiling 29% ferric chloride solution (12mL 
commercial 60% ferric chloride solution plus 13mL 
distilled water) and boil the solution for a 
further 3 minutes. Cool. After cooling filter it. 
Dry the filtrate on the filter paper in a 56øC 
oven until completely dry. Dissolve the dried 
filtrate in 400mL of 70% alcohol. Finally add 4mL 
concentrated hydrochloric acid and 6g phenol. It 
is best to leave this solution to mature for at least two weeks prior to use.

(B) NUCLEAR FAST RED
Dissolve 0.5g nuclear fast red in 500mL of warmed 
5% aluminium sulphate. Filter when cool.

(C) 4% AQUEOUS SODIUM METABISULPHITE

PROCEDURE
1. Deparaffinize and hydrate to distilled water.
2. Treat with acidified potassium permanganate 
(as for Gordon and Sweet's Reticular fibres method 2.4) for 5 minutes.

3. Treat with 4% sodium bisulphite for 1 minute.
4. Wash in running tap water.
5. Wash well with 70% alcohol.
6. Stain in the Victoria Blue solution, in a 
Coplin jar, for a minimum of 4 hours (preferably overnight).
7. Wash well with 70% alcohol for approx 1 
minute. This is the differentiation step - ensure 
the background of the section is clear.

8. Wash in running tap water for 1 minute.
9. Stain with nuclear fast red solution for 5 minutes.
10. Wash in running water for 2 minutes.
11. Dehydrate, clear and mount.

RESULTS
HBsAg, elastic fibres, copper associated protein blue
All other tissue components pink/red

HEALTH AND SAFETY
Potassium permanganate Harmful by ingestion. 
Irritating to eyes and skin Ferric chloride 
Irritant. Hydrochloric acid Vesicant. Causes 
burns. Phenol Harmful by ingestion. Irritating to eyes and skin.









At 12:30 PM 11/4/2009, Justin Peters wrote:

One of my pathologists has requested that we start offering a Victoria
Blue stain for liver specimens.  I am unfamiliar with this stain and was
wondering if anyone had a protocol for this that works well?  Thanks in
advance for any help :-)



Justin Peters, HTL (ASCP)

IHC Supervisor

Bostwick Laboratories(tm)
For Absolute Confidence(r)

4355 Innslake Drive
Glen Allen, Virginia 23060
Phone:(804) 967-9225 ext. 1831
Cell:(804) 822-6084
Email: jpet...@bostwicklaboratories.com
mailto:jpet...@bostwicklaboratories.com



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RE: [Histonet] misleading message on Histonet last Friday

2009-07-13 Thread LuAnn Anderson

I received the message on Friday


At 02:35 PM 7/13/2009, Mike Pence wrote:

I did not receive this message and have not seen this message come up in
the last several weeks.
Are you sure this came on the listserv?

Mike

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of LINDA
MARGRAF
Sent: Monday, July 13, 2009 1:41 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] misleading message on Histonet last Friday


Dear Histonetters:
I got the message below privately from one of the list members and (with
their permission) wanted to pass it along to the membership.

Dear Linda:
Matthew Semovoski [histosea...@gmail.com] posted this on Histonet this
AM: Hey everyone,  I am looking at getting some supplies for a new
histology lab. Has anyone ever purchased from Gorilla Scientific?
www.GorillaScientific.com  I just got a flyer in the mail from them and
it seems like they have some really good prices. I think I can save a
lot on my slides if I purchase from them. Has anyone else on here
purchased anything from them?  Thanks,  Alex histosea...@gmail.com
Well it was not Alex who posted it was Matthew Semovoski who posted this
 he is the man who answers the phone when you call up Gorilla
Scientific. I as a sales person play fair  do not try to do any slick
sales adds on histonet  wanted to make you aware of this. (I really am
such a geek  LOVE TO LEARN from Histonet too!) So I really do want to
thank you for all of the hard work that you do  just wanted to make you
aware of this instance. Thank you so much  have a great weekend!


I don't want to turn this into a major discussion but would like to
remind everyone that we run Histonet using University of Texas resources
and they would not appreciate (or support) its use for commercial
advertising even if it is disguised in a misleading message. Thank you,
Linda M Histonet administrator



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