[Histonet] Any help for this oil red o paper

2009-07-20 Thread abi jag
Dear histonetters,

Can anybody will help me with the following oil red o paper from Charles 
Churukian.

Journal of Histotechnology, 22(4):309-311 Charles Churukian, Lillie's Oil Red O 
method for neutral lipids.
I am not able to access the NSH site,the following error message is coming.
 
(ERROR: Specified ROOT dir [/var/www/html/live/tools/htdocs/newsite_templates/] 
is not a directory) 
Thanks

abijag





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[Histonet] anyone tried to get onto the NSH website today?

2009-07-20 Thread Kim Merriam
Good morning everyone,

I have tried several times to get onto the NSH website today and I keep getting 
an error.  I am wondering if it is down or if there is something wrong on my 
end.

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



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[Histonet] Part Time Position In Surprise, AZ

2009-07-20 Thread Alyssa Peterson
Good Morning All,

I have an immediate opening for a Histotechnician/Histotechnologist
candidate in Surprise, AZ. The position would require the qualified
candidate to work 2 days/week. 7:30am-5:00pm. HT ASCP is required, and 2+
years experience required as well. To apply please send an updated copy of
your resume for prescreening purposes, *All inquires are kept confidential*
following resume submitted you will be contacted to set up an initial phone
screen. Thank you in advance for any inquiries. :-)

-- 
*Be sure to visit us on the web* www.alliedsearchpartners.com
Alyssa Peterson, Director Of Recruitment
Allied Search Partners
O:888.388.7571 ext. 101
F: 888.388.7572
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[Histonet] NSH Website Down?

2009-07-20 Thread Breeden, Sara
I just tried the NSH website, and it seems to be down so it must not be
us... J  I'm sure someone has contacted them.

 

Sally Breeden, HT(ASCP)

NM Dept. of Agriculture

Veterinary Diagnostic Services

PO Box 4700

Albuquerque, NM  87106

505-841-2576

 

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Re: [Histonet] Any help for this oil red o paper

2009-07-20 Thread John Kiernan
Try
http://www.urmc.rochester.edu/path/zqu/StainsManual/index.html?OILREDOMETHODFORFATS
This is from the latest version of Chuck Churukian's lab manual; I think the 
method is the same as in his 1999 paper in J. Histotechnol.
 
John Kiernan
Anatomy, UWO
London, Canada
= = =
- Original Message -
From: abi jag abija...@yahoo.co.in
Date: Monday, July 20, 2009 7:30
Subject: [Histonet] Any help for this oil red o paper
To: histonet@lists.utsouthwestern.edu

 Dear histonetters,
 
 Can anybody will help me with the following oil red o paper from 
 Charles Churukian.
 
 Journal of Histotechnology, 22(4):309-311 Charles Churukian, 
 Lillie's Oil Red O method for neutral lipids.
 I am not able to access the NSH site,the following error message 
 is coming.
  
 (ERROR: Specified ROOT dir 
 [/var/www/html/live/tools/htdocs/newsite_templates/] is not a 
 directory) 
 Thanks
 
 abijag
 
 
 
 
 
   Looking for local information? 
 Find it on Yahoo! Local http://in.local.yahoo.com/
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Re: [Histonet] anyone tried to get onto the NSH website today?

2009-07-20 Thread Freida Carson
As of 11:30 CDT the NSH site is up and running or at least I did not have a 
problem getting it to come up.
 
Freida Carson

--- On Mon, 7/20/09, Kim Merriam kmerriam2...@yahoo.com wrote:


From: Kim Merriam kmerriam2...@yahoo.com
Subject: [Histonet] anyone tried to get onto the NSH website today?
To: Histonet histonet@lists.utsouthwestern.edu
Date: Monday, July 20, 2009, 7:46 AM


Good morning everyone,

I have tried several times to get onto the NSH website today and I keep getting 
an error.  I am wondering if it is down or if there is something wrong on my 
end.

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



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[Histonet] marilyn weiss will be out of the office

2009-07-20 Thread Marilyn . A . Weiss

I will be out of the office starting  07/20/2009 and will not return until
07/21/2009.

I will respond to your message when I return.In my absence please ask for
Mary Campbell or Laurie at 619-528-6801  if this is urgent they  can
contact me or give you my cell phone number.


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[Histonet] Fluorescent dyes and xylene

2009-07-20 Thread Bob Nienhuis
Will the Alexa Fluor dyes withstand some dehydration and clearing in
alcohol and xylene?

If they won't are there any bright fluorescent dyes that can be obtained
congugated to a secondary antibody that will?

Looking to immunostain tyrosine hydroxylase in rodent brain with
a fluorescent marker in tissue that needs to be dehydrated and
cleared, perhaps with an abbreviated series.

Bob Nienhuis
VA / UCLA Neurobiology Research
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Re: [Histonet] Fluorescent dyes and xylene

2009-07-20 Thread Merced M Leiker
So you are saying that you cannot just mount the brain tissue in aqueous 
mounting medium at the end (after washing the excess secondary antibody)? 
You must dehydrate and clear before mounting (in a permament medium)?  Just 
curious...


Merced

--On Monday, July 20, 2009 10:37 AM -0700 Bob Nienhuis 
bob.nienh...@gmail.com wrote:



Will the Alexa Fluor dyes withstand some dehydration and clearing in
alcohol and xylene?

If they won't are there any bright fluorescent dyes that can be obtained
congugated to a secondary antibody that will?

Looking to immunostain tyrosine hydroxylase in rodent brain with
a fluorescent marker in tissue that needs to be dehydrated and
cleared, perhaps with an abbreviated series.

Bob Nienhuis
VA / UCLA Neurobiology Research
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Merced M Leiker
Research Technician II
Cardiovascular Medicine
348 Biomedical Research Building
State University of New York at Buffalo
3435 Main St, Buffalo, NY  14214
lei...@buffalo.edu
716-829-6118 (Ph)
716-829-2665 (Fx)

No trees were harmed in the sending of this email.
However, many electrons were severely inconvenienced.


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[Histonet] HELP Starting a lab

2009-07-20 Thread Kimberly Tuttle
I have a friend who is a Pathologist and starting a new lab. She sent me a list 
of start up supplies and equipment that she needs to purchase. Can I get some 
input on whats missing from her list, I've added a few things but Im going 
blank. Its a hisology lab for a urology practice if that helps. Thank you in 
advance!

PLEASE VENDORS DONT CALL OR EMAL ME

Equipment:
Negative pressure hood for grossing of specimens (grossing station)
Refrigerator w/freezer or separate freezer
Cassette labeler
Tissue processor
Embedding Stations
Microtomes
Waterbaths,  1 per microtome
Automatic HE stainer
A scale and a mixing/heating plate
Manual staining dishes, and slide holders that fit in them.
Slide and block storage system

Supplies:
Safety equipment like goggles and sleeve covers, aprons, a flame cabinet for 
flammable liquids 
acid cabinet?
Blades
Forceps
Rulers
Hemostats
Scissors
Glassware like flasks, beakers, graduated cylinders, and a funnel.Pipettes and 
tips.

Reagents:
Formalin
70% etoh
95% etoh
100% etoh
xylene 
paraffin
Hematoxylin stain
Eosin stain


Kimberly C. Tuttle  HT (ASCP)
Pathology Biorepository and Research Core
University of Maryland 
Room NBW58, UMMC
22 S. Greene St
Baltimore, MD 21201
(410) 328-5524
(410) 328-5508 fax 
Please consider the environment before printing this e-mail.


 

This e-mail and any accompanying attachments may be privileged, confidential, 
contain protected health information about an identified patient or be 
otherwise protected from disclosure. State and federal law protect the 
confidentiality of this information. If the reader of this message is not the 
intended recipient; you are prohibited from using, disclosing, reproducing or 
distributing this information; you should immediately notify the sender by 
telephone or e-mail and delete this e-mail.


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[Histonet] Re: Fluorescent dyes and xylene

2009-07-20 Thread Bob Nienhuis
Sorry, I should have mentioned that this will be done on thick frozen
sections.

Bob

On Mon, Jul 20, 2009 at 10:37 AM, Bob Nienhuis bob.nienh...@gmail.comwrote:

 Will the Alexa Fluor dyes withstand some dehydration and clearing in
 alcohol and xylene?

 If they won't are there any bright fluorescent dyes that can be obtained
 conjugated to a secondary antibody that will?

 Looking to immunostain tyrosine hydroxylase in rodent brain with
 a fluorescent marker in tissue that needs to be dehydrated and
 cleared, perhaps with an abbreviated series.

 Bob Nienhuis
 VA / UCLA Neurobiology Research


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Re: [Histonet] Re: Fluorescent dyes and xylene

2009-07-20 Thread Bader Siddiki
Hello
My experience is that most Immunofluorescence dyes do not withstand alcohol
and organic solvents dehydration.
You can use aqueous mounting medium with anti-fading agent.
Frozen brain tissue is tough to work with;  since it contains tons of
lipids.
Lots of mounting mediums will produce air bubbles because aqueous mounting
medium being hydrophilic and brain tissue being hydrophobic.
We are in the process of developing an aqueous mounting medium with
anti-fading agent and should be OK to use with tissue like brain, if
interested please let us know we can send you a sample for evaluation.
Bader

On Mon, Jul 20, 2009 at 11:22 AM, Bob Nienhuis bob.nienh...@gmail.comwrote:

 Sorry, I should have mentioned that this will be done on thick frozen
 sections.

 Bob

 On Mon, Jul 20, 2009 at 10:37 AM, Bob Nienhuis bob.nienh...@gmail.com
 wrote:

  Will the Alexa Fluor dyes withstand some dehydration and clearing in
  alcohol and xylene?
 
  If they won't are there any bright fluorescent dyes that can be obtained
  conjugated to a secondary antibody that will?
 
  Looking to immunostain tyrosine hydroxylase in rodent brain with
  a fluorescent marker in tissue that needs to be dehydrated and
  cleared, perhaps with an abbreviated series.
 
  Bob Nienhuis
  VA / UCLA Neurobiology Research
 
 
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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 /
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)
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RE: [Histonet] HELP Starting a lab

2009-07-20 Thread JR R

Pretty good list.

Don't forget first aid kits and spill kits.

Jerry Ricks
Research Scientist
University of Washington
Department of Pathology

 Date: Mon, 20 Jul 2009 14:26:57 -0400
 From: ktut...@umm.edu
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] HELP Starting a lab
 
 I have a friend who is a Pathologist and starting a new lab. She sent me a 
 list of start up supplies and equipment that she needs to purchase. Can I get 
 some input on whats missing from her list, I've added a few things but Im 
 going blank. Its a hisology lab for a urology practice if that helps. Thank 
 you in advance!
 
 PLEASE VENDORS DONT CALL OR EMAL ME
 
 Equipment:
 Negative pressure hood for grossing of specimens (grossing station)
 Refrigerator w/freezer or separate freezer
 Cassette labeler
 Tissue processor
 Embedding Stations
 Microtomes
 Waterbaths,  1 per microtome
 Automatic HE stainer
 A scale and a mixing/heating plate
 Manual staining dishes, and slide holders that fit in them.
 Slide and block storage system
 
 Supplies:
 Safety equipment like goggles and sleeve covers, aprons, a flame cabinet for 
 flammable liquids 
 acid cabinet?
 Blades
 Forceps
 Rulers
 Hemostats
 Scissors
 Glassware like flasks, beakers, graduated cylinders, and a funnel.Pipettes 
 and tips.
 
 Reagents:
 Formalin
 70% etoh
 95% etoh
 100% etoh
 xylene 
 paraffin
 Hematoxylin stain
 Eosin stain
 
 
 Kimberly C. Tuttle  HT (ASCP)
 Pathology Biorepository and Research Core
 University of Maryland 
 Room NBW58, UMMC
 22 S. Greene St
 Baltimore, MD 21201
 (410) 328-5524
 (410) 328-5508 fax 
 Please consider the environment before printing this e-mail.
 
 
  
 
 This e-mail and any accompanying attachments may be privileged, confidential, 
 contain protected health information about an identified patient or be 
 otherwise protected from disclosure. State and federal law protect the 
 confidentiality of this information. If the reader of this message is not the 
 intended recipient; you are prohibited from using, disclosing, reproducing or 
 distributing this information; you should immediately notify the sender by 
 telephone or e-mail and delete this e-mail.
 
 
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[Histonet] Celloidin Sections.

2009-07-20 Thread JR R


I am curious--How thin can celloidin sections be cut?  I've heard that 30 
microns is a standard thickness.  No way to make 5 micron sections?

Thanks,


Jerry Ricks
Research Scientist
University of Washington
Department of Pathology

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RE: [Histonet] Celloidin Sections.

2009-07-20 Thread Rittman, Barry R
Jerry
depends on whether you are talking about celloidin or Low Viscosity 
Nitrocelulose.
There are techniques in the literature to cut celloidin sections as thin  as 4 
microns.
For LVN you need much thicker sections as this plastic is much less sturdy and 
has a tendency to fragment if too thin.
The questions I ask is why you need celloidin sections and what tissue are you 
thinking about for this technique?
Barry


From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of JR R 
[rosenfeld...@hotmail.com]
Sent: Monday, July 20, 2009 6:42 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Celloidin Sections.

I am curious--How thin can celloidin sections be cut?  I've heard that 30 
microns is a standard thickness.  No way to make 5 micron sections?

Thanks,


Jerry Ricks
Research Scientist
University of Washington
Department of Pathology

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[Histonet] double immunostaining with antigen retrieval and no antigen retrieval

2009-07-20 Thread Cathy Malcontenti-Wilson
Dear All,

Is it possible to do double immunostaining for one antibody which
doesn't require antigen retrieval, and the other one which doesn't need
it.  Can you do the one without retrieval first, then retrieve and do
the other one, or does the retrieval damage the first staining? We know
that doing antigen retrieval for antibody that doesn't require it gives
us non specific staining. 

 

I would appreciate some advice.

 

Thank you very much.
Cathy Malcontenti-Wilson

 

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