Re: [Histonet] HMGB and RAGE; TLR2, TLR4 antibodies

2010-10-04 Thread Fabrice GANKAM
thanks Amos
which one did you used ? you have catalog number ?

On Fri, Oct 1, 2010 at 9:44 PM, Amos Brooks amosbro...@gmail.com wrote:

 Hi,
  I am currently working on HMGB1. It is a weird one! If you go by the
 data sheets you will get great nuclear staining on all the nuclei. This is
 not what you are after if you have necrotic tissue. What you want to see is
 the nuclei in necrotic tissue fade out and have the cytoplasm take it up. I
 am cutting the dilution to 1: 50 and 1:100 since we were just starting to
 see blushes of cytoplasmic staining and no nuclear label at higher
 dilutions. Usually you get staining that fades out at higher dilutions. This
 one was really odd.

 Good luck,
 Amos


 Message: 13
 Date: Thu, 30 Sep 2010 04:55:02 +0200
 From: Fabrice GANKAM gan...@googlemail.com
 Subject: [Histonet] HMGB and RAGE; TLR2, TLR4 antibodies
 To: histonet@lists.utsouthwestern.edu
 Message-ID: c4a46c631cd14a86aad3ce3abb29a...@pcdegankam
 Content-Type: text/plain;   charset=us-ascii


 Hey guys
 Just wanted to know if any of you had some luck with an antibody aigainst
 rat HMGB1 and its receptors RAGE, TLR2, TLR4.
 W
 Thanks
 Dr Fabrice GANKAM
 UTSW

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[Histonet] 3-6 month temp position in Gaithesburg Maryland

2010-10-04 Thread Madary, Joseph
`HT or HTL ASCP-tech will perform duties in a veterinary histology lab
at Medimmune in Gaithersburg Md.  Tech should be able to perform
full-tissue necropsies on rodents, subsequent trimming, perform manual
and automated tissue processing, decals, embedding in OCT and paraffin,
microtomy and cryotomy, manual and automated HE staining and
coverslipping.  Should be proficient in manually performed special
stains and immunohistochemistry.  Should possess excellent
troubleshooting skills, be familiar with GLP procedures and
documentation.  Tech should be clean and organized in the performance of
his or her duties.  The tech will be an Aerotek employee/contractor for
Medimmune, not a Medimmune employee.  This would be a straight up temp
position, no benefits such as 401K, medical or dental.  20-40 hours per
week.  Perfect position for a person in between jobs, semi-retired etc.
If you bring an exceptional set of skills with you but do not possess
one of the skills listed above, we may work around that say you are
excellent at necropsy but are not good at specials or IHC.  Please
submit resumes to Aerotek on your won to get the ball rolling, and then
send a resume for the hiring manager Nick Madary at
mada...@medimmune.com.

 

 

 

Nick Madary, HT/HTL(ASCP)QIHC

Histology Mgr, Medimmune

301.398.6360(lab), 4745(vm),9745(fax)

 

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[Histonet] PI for Pathologists

2010-10-04 Thread Laurie Colbert
Our pathologists do not like the CAP survey for their performance
improvement program in Surgical Pathology.  Does anyone know of any
other company/organization that might offer something like this for our
pathologists?

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[Histonet] Direct immunofluoresent question

2010-10-04 Thread bamoe

Hi all -

The pathologist that reads our direct IF slides likes to have the sections
of tissue circled on the slide so that they are easier to find.  We
currently use black marker on the back of the slide, but find that many
times it smears and are looking for a better solution.

What kind of slides do others use, and if you circle your sections what
marker/pen/etcher do you use?

Any thoughts are greatly appreciated!

Barb Moe
Gundersen Lutheran Medical Center
La Crosse WI


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[Histonet] DIF Transport Media

2010-10-04 Thread kristen arvidson
Is Michel Medium the same as Zeus?  Do these need to be refrigerated?
Thanks.



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Re: [Histonet] Direct immunofluoresent question

2010-10-04 Thread Rene J Buesa
I used to mark on the slide, around the section, with a wax marker. Once dried 
and the procedure completed, cover and observe.
René J.

--- On Mon, 10/4/10, ba...@gundluth.org ba...@gundluth.org wrote:


From: ba...@gundluth.org ba...@gundluth.org
Subject: [Histonet] Direct immunofluoresent question
To: histonet@lists.utsouthwestern.edu
Date: Monday, October 4, 2010, 1:49 PM



Hi all -

The pathologist that reads our direct IF slides likes to have the sections
of tissue circled on the slide so that they are easier to find.  We
currently use black marker on the back of the slide, but find that many
times it smears and are looking for a better solution.

What kind of slides do others use, and if you circle your sections what
marker/pen/etcher do you use?

Any thoughts are greatly appreciated!

Barb Moe
Gundersen Lutheran Medical Center
La Crosse WI


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[Histonet] IHC unfixed human brain tissue

2010-10-04 Thread Neil M. Fournier
I have limited experience working with human brain tissue and would like to
stain some human brain sections that I received. They were not fixed, but were
flash frozen and sectioned on a cryostat, and mounted onto slides.

Could someone give me a brief run down of their standard methodological staining
procedure with unfixed human brain sections?

Much appreciated

Neil

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[Histonet] Re: PI for Pathologists

2010-10-04 Thread Robert Richmond
From: Laurie Colbert laurie.colb...@huntingtonhospital.com
Subject: [Histonet] PI for Pathologists
Laurie Colbert at Huntington Hospital in Pasadena CA asks:

Our pathologists do not like the CAP survey for their performance improvement 
program in Surgical Pathology.  Does anyone know of any other 
company/organization that might offer something like this for our 
pathologists?

Do your pathologists have any input into this decision? I think there
are some local programs in California. You're probably referring to
the PIP - the Performance Improvement Program in Surgical Pathology
of the College of American Pathologists. I've subscribed since 1993
and have never thought very much of it. The CAP need to avail
themselves of the new virtual slide technology (such as Aperio's) -
this will become more attractive with the new DICOM image standards
for pathology - and re-do the PIP program.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] Re: Marking inks

2010-10-04 Thread Tony Henwood
The following might be of use

Marking surgical margins are often required for determining the adequacy
of excision of lesions. Sometimes up to 6 margins (medial, lateral,
superior, inferior, superial and deep margins) are required to be
individually marked.

The properties of a good marker include:

1.  It is quick to dry. 
2.  It is easy to apply. 
3.  It has a long shelf life. 
4.  It is cheap. 
5.  It is non-toxic. 
6.  It does not spread beyond the edge of the marked area. 
7.  It is preserved during processing (no contamination of
solutions). 
8.  It is visible macroscopically and microscopically. 
9.  Sectioning is not affected. 
10. It is radiolucent. 
11. There are multiple colours available.

India Ink, a colloidal suspension of particulate carbon in aqueous gum
has been used for many years, but is messy, slow to dry and spreads
readily over the tissue surface. 10% Silver Nitrate in methanol has been
suggested but it also spreads over the surface and is macroscopically
invisible.

5% alcian blue in 80% ethanol is an excellent tissue marker. It is easy
to apply, quick to dry, has a long shelf life and is preserved during
processing.

Birch et al (1990) have suggested that specimens can be dunked into 1%
aqueous alcian blue. This method is quick, cheap and the coating is
radiolucent.

Harris (1990) has suggested the use of Tippex fluid. This is a solution
of titanium dioxide and polyacrylate in trichloethane. It has a long
shelf life, is easy to use, quick drying, non-toxic and the tissue
processor is not affected. The marker does however have a tendency to
lift and is radiodense.

Hunter-Craig et al (1991) rolled blotted dry specimens in starch powder.
The surface coating of starch is visible on light microscopy but
strikingly apparent if crossed polarisers are used.

Artist's pigments in acetone (a 50% solution) were used by Patterson and
Davies (1988). The pigments are quick drying, have a good range of
different colours that are visible both macroscopically and
microscopically (especially using polarised light) and are resistant to
processing. They are however, radiodense and have a short storage life.
It must be remembered that the dry powders (which contain cobalt,
manganese and cadmium) are toxic. The pigment granules are also of
similar size and density to microcalcification and there may be
confusion on subsequent specimen mammography after tissue slicing.

Suggested pigments are as follows:

PIGMENT   COLOURMACROSCOPIC MICROSCOPIC
Cobalt Blue BlueBlue
Alizarin CrimsonRed Red 
ViridianGreen   Green

Armstrong et al (1990) have described the use of organically coloured
gelatines, where 8% solution of dye is prepared in 24% aqueous gelatine.
They found it easier to discriminate between colours of particulate dyes
(i.e. plant substances), with the gelatine staining with both
haematoxylin and eosin giving a pink to purple colour. They found clear
demarcation between two adjacent colours and only a modest knowledge of
botany was required for the identification of the three plant materials.


DYE COLOUR  MACROSCOPIC MICROSCOPIC
Janus Green BluePurple 
India Ink   Black   Black  
Paprika Red/brown   Red-pigmented cellulose 
Tumeric Yellow  Cerebriform starch granules
Henna   Brown   Brown-pigmented cellulose
Bismark Brown   Brown   Brown particles

Unfortunately tumeric causes knife scratching.

Armstrong et al (1990) J.Clin.Pathol., 43:604-607
Birch et al (1990) J.Clin.Pathol 43:608-609
Harris (1990) J.Clin.Pathol 43:346
Hunter-Craig et al (1991) J.Clin.Pathol. 44:874-875
Patterson  Davies (1988) J.Clin.Pathol 41:1013-1016


Regards

Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC)
Laboratory Manager  Senior Scientist
Tel: 612 9845 3306
Fax: 612 9845 3318
the children's hospital at westmead 
Cnr Hawkesbury Road and Hainsworth Street, Westmead 
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA 




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Robert
Richmond
Sent: Saturday, 2 October 2010 3:48 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Marking inks


Richard Cartun asks about marking inks used for surgical pathology
specimens.

if I just need one color (great majority of specimens) I use india ink
bought from a stationer or craft supply store - cheap, easily replaced,
and it gets the job done.

If I need colors, I prefer the Davidson marking inks, available through
some though not all vendors. They offer seven colors, including orange
(they have to sell their product in Tennessee and Texas, after all!) and
purple. (I have no commercial connection with Davidson inks.)

I blot my specimens thoroughly dry, and don't use a fixative. If I did,
I'd use white vinegar (5% acetic acid), possibly diluted 1:1 with water.
Bouin's fixative and acetone both have obvious 

[Histonet] CAP programs

2010-10-04 Thread Tench, Bill
There are now online CAP PIP programs.  I have done one on prostate.
Also there are online programs for the cytology part.  Review the
catalogue.
 
Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604
 

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