[Histonet] Equipment Maintenance

2009-02-06 Thread Bradley Rodriguez
Can anyone recommend a good East Coast histo equipment maintenance company?

 

Regards,

Brad

 

Bradley Rodriguez 
Histology Coordinator 
HSRL (Histo-Scientific Research Laboratories) 
5930 Main Street 
Mount Jackson, VA 22842 
540.477.4440 
Fax: 540.477.4448 
b...@hsrl.org 
www.hsrl.org 

***Confidentiality Notice: 
This e-mail is strictly confidential and intended solely for the addressee.
If you are not the intended recipient you must not use, disclose, or copy
this transmission. If you have received this message in error, please
contact the sender and delete the material from any computer, disc drive,
diskette, or other storage device or media. 

 

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Mountant for GMA stained sections

2009-02-06 Thread Pamela Marcum
I agree with Gayle.  We put a weight on the coverslip until it dries to help
keep it flat.  Since all mounting media has some organic solvent like xylene
or toluene it is hard to avoid them completely.  We use DPX for everything
here.

Best Regards,

Pamela A Marcum
University of Pennsylvania 
School of Veterinary Medicine
Comparative Orthopedic Laboratory (CORL)
382 W Street Rd
Kennett Square PA 19438
610-925-6278

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of gayle callis
Sent: Friday, February 06, 2009 9:46 AM
To: 'Histonet'; ' Histonet messages replies'
Subject: [Histonet] Mountant for GMA stained sections

Let stained GMA sections  air dry and mount with a permanent mounting media.
Dipping in xylene tends to crack or cause the GMA to wrinkle since the
plastic can't be removed.  

 

Gayle M. Callis 

HTL(ASCP)HT,MT

Bozeman MT

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Opinions and any problems with Leica IPC

2009-02-06 Thread Stephen.Eyres
Hi,
 
I'd be really grateful for feedback from small labs using a Leica IPC on
consistency, and in problems.
 
Thanks
 
Steve
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Re: Paraffin Blocks

2009-02-06 Thread Weems, Joyce
We have so many malignant patients here that a week after I discarded
blocks through 1984 (this was several years ago), I had a patient call
for a block. When she said, Well, I just wasn't supposed to live this
long I just cried. All I could do was apologize but I don't want to
have to tell patients that any more!  We have been sending out KRAS,
BRAF and EGFR mutations on cases from the 90s just this past week - we
can hardly keep up there are so many requests for these new tests. And I
expect it will only increase just like Bob said..more of my 2
cents!!! j



From: Bonner, Janet [mailto:janet.bon...@flhosp.org] 
Sent: Friday, February 06, 2009 8:50 AM
To: Weems, Joyce; Robert Richmond; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Paraffin Blocks


We are a very large facility and kept the majority of our blocks and
slides in a minimally air-conditioned hospital supplies warehouse.  I
used to pull blocks and slides for legal cases, and it was
rare-rare-rare that anyone did anything with the blocks after five
years.  Ten years for the slides was appropriate.
 Janet
 
Janet L. Bonner, HTL (ASCP)
Pathology Laboratory


From: histonet-boun...@lists.utsouthwestern.edu on behalf of Weems,
Joyce
Sent: Thu 2/5/2009 6:12 PM
To: Robert Richmond; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Paraffin Blocks



I've been preaching this sermon for several years!!!  We must do
something!!!  j


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Robert
Richmond
Sent: Thursday, February 05, 2009 5:28 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Paraffin Blocks

How long to retain paraffin blocks (human tissue) is an issue that's
going to need re-thinking.

Presently most pathology services in the USA retain them for no more
than ten years. If the laboratory closes, slides and blocks are disposed
of immediately.

It seems to me that in the coming age of molecular pathology, there will
be a lot more interest in recovering paraffin blocks after longer
periods of time. I think that the regulatory agencies will soon need to
address this problem.

Storing present-day paraffin blocks, with their bulky plastic mounts and
low-melting waxes, is going to become even more difficult than it is
now, as hospitals and other facilities consider the cost of maintaining
and cooling storage space.

I don't think it's possible to triage blocks and slides for disposal at
the time the case is signed out. It sounds like a good idea, but the few
times I've seen it tried it didn't work. Also, we really don't know what
we're going to need to recover in the future.

Bob Richmond
Samurai Pathologist (nearly 70, isn't going to have to worry about this
problem) Knoxville TN

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Confidentiality Notice:
This email, including any attachments is the
property of Catholic Health East and is intended
for the sole use of the intended recipient(s). 
It may contain information that is privileged and
confidential.  Any unauthorized review, use,
disclosure, or distribution is prohibited. If you are
not the intended recipient, please reply to the
sender that you have received the message in
error, then delete this message.


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


===
The information contained in this message may be privileged and/or
confidential
and protected from disclosure.  If the reader of this message is not the
intended 
recipient or an employee or agent responsible for delivering this
message to the 
intended recipient, you are hereby notified that any dissemination,
distribution 
or copying of this communication is strictly prohibited.  If you have
received this
communication in error, please notify the sender immediately by replying
to this 
message and deleting the material from any computer.
===

Confidentiality Notice:
This email, including any attachments is the 
property of Catholic Health East and is intended 
for the sole use of the intended recipient(s).  
It may contain information that is privileged and 
confidential.  Any unauthorized review, use,
disclosure, or distribution is prohibited. If you are 
not the intended recipient, please reply to the 
sender that you have received the message in 
error, then delete this message.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Equipment Maintenance

2009-02-06 Thread Smith Wanda
Southeast Pathology Instrument Services, Inc based out of Folly Beach, SC.  
Michael Dietrich is the BEST! And so are the guys that work for him!!!
843-588-2559
843-708-7090 Michael's cell #
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

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bradley 
Rodriguez
Sent: Friday, February 06, 2009 10:04 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Equipment Maintenance

Can anyone recommend a good East Coast histo equipment maintenance company?

 

Regards,

Brad

 

Bradley Rodriguez
Histology Coordinator
HSRL (Histo-Scientific Research Laboratories) 5930 Main Street Mount Jackson, 
VA 22842 540.477.4440
Fax: 540.477.4448
b...@hsrl.org
www.hsrl.org 

***Confidentiality Notice: 
This e-mail is strictly confidential and intended solely for the addressee.
If you are not the intended recipient you must not use, disclose, or copy this 
transmission. If you have received this message in error, please contact the 
sender and delete the material from any computer, disc drive, diskette, or 
other storage device or media. 

 

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Disinfecting Cryostat

2009-02-06 Thread Louise Hartson
Can someone suggest a good universal method for disinfecting the Cryostat
after each use?
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] RE: Histonet Digest, Vol 63, Issue 7

2009-02-06 Thread Terri Braud
Ditto - 
We really like our Glas coverslipper and LOVE their coverslipping media.  Its 
perfect for their machine, and dries very quickly. We usually file in 2 days 
time, air dried only.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
   2. RE: Mounting media question (Molinari, Betsy)
 

I use Sakura Tissue Tek Glas mounting media. I can file the next day.
Betsy Molinari HT(ASCP)
-Original Message-

Subject: [Histonet] Mounting media question


We will soon be receiving our new Sakura Glas Coverslipper. Can anyone
who is also using this instrument please tell me what type of mounting
media is being used.
We are looking for a fast-drying media that can be used for tissue
slides, non-gyne and gyne slides. We are also looking at long term
storage without fading capability.
Our current mounting media - Surgipath's Micromount used on the older
model Sakura -Glas coverslipper does not dry quickly. Storage and slide
handling issues around this problem.
Thank you,

Karen J Kay, MLT
Pathology Supervisor
Chinook Health Laboratory
Chinook Regional Hospital


-



CONFIDENTIALITY NOTICE:

This E-Mail is intended only for the use of the individual or entity to which
it was sent. It may contain information that is privileged and/or confidential,
and the use or disclosure of such information may also be restricted under 
applicable
federal and state law. If you received this communication in error, please do 
not
distribute any part of it or retain any copies, and delete the original E-Mail.
Please notify the sender of any error by E-Mail.

Thank you for your cooperation.

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Mountant for GMA stained sections

2009-02-06 Thread gayle callis
Let stained GMA sections  air dry and mount with a permanent mounting media.
Dipping in xylene tends to crack or cause the GMA to wrinkle since the
plastic can't be removed.  

 

Gayle M. Callis 

HTL(ASCP)HT,MT

Bozeman MT

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] RE: Disinfecting Cryostat

2009-02-06 Thread Podawiltz, Thomas
I believe CAP recommends 70% etoh.


Tom Podawiltz, HT (ASCP)
Histology Section Head/Laboratory Safety Officer
LRGHealthcare
603-524-3211 ext: 3220

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Louise Hartson 
[louise_hart...@urmc.rochester.edu]
Sent: Friday, February 06, 2009 10:42 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Disinfecting Cryostat

Can someone suggest a good universal method for disinfecting the Cryostat
after each use?
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
THIS MESSAGE IS CONFIDENTIAL.  
This e-mail message and any attachments are proprietary and confidential 
information intended only for the use of the recipient(s) named above. If you 
are not the intended recipient, you may not print,distribute, or copy this 
message or any attachments.  If you have received this communication in error, 
please notify the sender by return e-mail and delete this message and any 
attachments from your computer. Any views or opinions expressed are solely 
those of the author and do not necessarily represent those of LRGHealthcare.


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Best Decal?

2009-02-06 Thread Cindy DuBois
What is the best decal to use for bone such as knee  femur?  We are
currently using Decalcifying H from Ever Scientific at the grossing area for
4 - 8 hours and Decal stat at the microtome for another 2 hours.  It seems
like there must be a better way?  Both the Decal H and the Decal Stat are
hydrochloric acid based.

Cindy Dubois
Integrated Pathology
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Re: Paraffin Blocks

2009-02-06 Thread Bernice Frederick
All
We are a tissue bank and heavily involved with clinical trials. We are
trying to find a way for people to flag cases on these trials that have
consented to future use so that when it comes time for block disposal,those
blocks are kept or sent to the appropriate group that ran and or banks the
tissue for that trial. We have translational studies as far back as 1990
that I ma afraid the rest of the case is gone.
Bernice


Bernice Frederick HTL (ASCP)
Northwestern University
Pathology Core Facility
ECOGPCO-RL 
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, Joyce
Sent: Thursday, February 05, 2009 5:13 PM
To: Robert Richmond; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Paraffin Blocks

I've been preaching this sermon for several years!!!  We must do
something!!!  j


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Robert
Richmond
Sent: Thursday, February 05, 2009 5:28 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Paraffin Blocks

How long to retain paraffin blocks (human tissue) is an issue that's
going to need re-thinking.

Presently most pathology services in the USA retain them for no more
than ten years. If the laboratory closes, slides and blocks are disposed
of immediately.

It seems to me that in the coming age of molecular pathology, there will
be a lot more interest in recovering paraffin blocks after longer
periods of time. I think that the regulatory agencies will soon need to
address this problem.

Storing present-day paraffin blocks, with their bulky plastic mounts and
low-melting waxes, is going to become even more difficult than it is
now, as hospitals and other facilities consider the cost of maintaining
and cooling storage space.

I don't think it's possible to triage blocks and slides for disposal at
the time the case is signed out. It sounds like a good idea, but the few
times I've seen it tried it didn't work. Also, we really don't know what
we're going to need to recover in the future.

Bob Richmond
Samurai Pathologist (nearly 70, isn't going to have to worry about this
problem) Knoxville TN

___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
Confidentiality Notice:
This email, including any attachments is the 
property of Catholic Health East and is intended 
for the sole use of the intended recipient(s).  
It may contain information that is privileged and 
confidential.  Any unauthorized review, use,
disclosure, or distribution is prohibited. If you are 
not the intended recipient, please reply to the 
sender that you have received the message in 
error, then delete this message.


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet



___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Disinfecting Cryostat

2009-02-06 Thread gayle callis
We use 70% ethanol on gauze (just damp) to wipe down inside of cryostat. Do
not use 95% or 100% alcohol, as 70% is the most effective for disinfection,
commonly used in biohoods. We pick up little trimmings with first dampened
gauze (or kim wipe) then re-wipe with a second gauze. We prefer gauze for
its flexibility.  Also, if you put a kimwipe or gauze behind knife holder to
l catch trimmings then you can fold up kimwipe, and lift garbage out,
intact, and go to biohazard container before wipe down.  We try to avoid too
much alcohol on knife holder parts since alcohol ruins lubricants needed for
good operation.  Check with your cryostat manufacturer to see what they
recommend.   It pays to wipe down under and over sliding glass door to
counterattack biohazardous cling-ons found on your gloves, and where
people have touched the instrument. 70% alcohol will not kill prions.  

Water based disinfectants freeze in cryostat. Eventually you need scheduled
disinfection with cryostat in defrosted mode with approved disinfecting
agent.  

Gayle M. Callis
HTL(ASCP)HT,MT
Bozeman MT 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Louise
Hartson
Sent: Friday, February 06, 2009 8:43 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Disinfecting Cryostat

Can someone suggest a good universal method for disinfecting the Cryostat
after each use?
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet



___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] Flammable storage

2009-02-06 Thread Webb, Dorothy L
How does everyone store any reagents that need refrigeration that are
also flammable? We have always just stored them in the routine histology
refrigerator.  I have never had this concern come up before and the
charge tech of toxicology is now questioning this type of storage.  Any
guidance on this would be greatly appreciated!!

Thanks, as always fellow histonetters, the best group in the world!!

Dorothy Webb, HT
Regions Histology Technical Supervisor
651-254-2962

This e-mail and any files transmitted with it are confidential and are intended 
solely for the use of the individual or entity to whom they are addressed. If 
you are not the intended recipient or the individual responsible for delivering 
the e-mail to the intended recipient, please be advised that you have received 
this e-mail in error and that any use, dissemination, forwarding, printing, or 
copying of this e-mail is strictly prohibited.
 
If you have received this e-mail in error, please immediately notify the 
HealthPartners Support Center by telephone at (952) 967-6600. You will be 
reimbursed for reasonable costs incurred in notifying us.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] RE: Flammable storage

2009-02-06 Thread Swain, Frances L
We have purchased a flammable or explosion proof refrigerator from Fisher 
Scientific.  The thermostat is on the outside of the cabinent not inside the 
cabinet.  This is very important for two reasons: 1) if you have flammable or 
ignitable reagents and you store then in a frost free refrigerator (regular 
Sears , etc refrigerator) you will run the risk of an explosion or fire.  We 
had this happen here at UAMS several years ago when some put a flammable 
reagent in a regular freezer.  When the compressor came on it blue the door off 
of the refrigerator and set the whole lab on fire.  You do not want to deal 
with this.  2) If you store your antibodies, kits, etc in a frost free or 
regular refrigerator it will destroy the antibody because a frost free 
refrigerator cycles and in cycling will heat up and make your antibody expire 
quicker.  I know that these special refrigerators are very expensive but if you 
have a lot of antibodies and kits, or if you have a lot of flammables that must 
be kept cold it is worth it. 

Frances L. Swain HT(ASCP) A. A. S.
Special Procedures Technician
Department of Orthopaedic Surgery
Center for Orthopaedic Research
Barton Research Building 2R28
4301 West Markham Street
Little Rock AR 72205
(501) 686-8739 PHONE
(501) 686-8987 FAX
swainfranc...@uams.edu email

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Webb, Dorothy L
Sent: Friday, February 06, 2009 1:36 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Flammable storage

How does everyone store any reagents that need refrigeration that are
also flammable? We have always just stored them in the routine histology
refrigerator.  I have never had this concern come up before and the
charge tech of toxicology is now questioning this type of storage.  Any
guidance on this would be greatly appreciated!!

Thanks, as always fellow histonetters, the best group in the world!!

Dorothy Webb, HT
Regions Histology Technical Supervisor
651-254-2962

This e-mail and any files transmitted with it are confidential and are intended 
solely for the use of the individual or entity to whom they are addressed. If 
you are not the intended recipient or the individual responsible for delivering 
the e-mail to the intended recipient, please be advised that you have received 
this e-mail in error and that any use, dissemination, forwarding, printing, or 
copying of this e-mail is strictly prohibited.
 
If you have received this e-mail in error, please immediately notify the 
HealthPartners Support Center by telephone at (952) 967-6600. You will be 
reimbursed for reasonable costs incurred in notifying us.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

Confidentiality Notice: This e-mail message, including any attachments, is for 
the sole use of the intended recipient(s) and may contain confidential and 
privileged information.  Any unauthorized review, use, disclosure or 
distribution is prohibited.  If you are not the intended recipient, please 
contact the sender by reply e-mail and destroy all copies of the original 
message.


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


RE: [Histonet] Best Decal?

2009-02-06 Thread Swain, Frances L
Hi Cindy:  We use 5% Formic Acid with a chemical end point test to determine 
when decalcification has been completed.  We make our own 5% Formic Acid but 
Newcomer's Supply has some that I have used which worked really well. If you 
have any questions please feel free to contact me.

Frances L. Swain HT(ASCP) A. A. S.
Special Procedures Technician
Department of Orthopaedic Surgery
Center for Orthopaedic Research
Barton Research Building 2R28
4301 West Markham Street
Little Rock AR 72205
(501) 686-8739 PHONE
(501) 686-8987 FAX
swainfranc...@uams.edu email

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cindy DuBois
Sent: Friday, February 06, 2009 10:56 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Best Decal?

What is the best decal to use for bone such as knee  femur?  We are
currently using Decalcifying H from Ever Scientific at the grossing area for
4 - 8 hours and Decal stat at the microtome for another 2 hours.  It seems
like there must be a better way?  Both the Decal H and the Decal Stat are
hydrochloric acid based.

Cindy Dubois
Integrated Pathology
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

Confidentiality Notice: This e-mail message, including any attachments, is for 
the sole use of the intended recipient(s) and may contain confidential and 
privileged information.  Any unauthorized review, use, disclosure or 
distribution is prohibited.  If you are not the intended recipient, please 
contact the sender by reply e-mail and destroy all copies of the original 
message.


___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


[Histonet] feulgen stain on brain sections

2009-02-06 Thread TF
Hi all, i amusing Feulgen staining to visualize the apoptotic cells on 20 um 
brain frozen sections.
The procedure is 5N HCl room temperature for 1.5 hour, wash in cool 1N HCl, 
wash in water, Schiff staining room temperature 1 h, wash throughly in 
distilled water, counterstain with 1% light green.

I have two questions here:
(1) after schiff staining, i can not visualize individual nucleui clearly, but 
all the section seems to be stained red.
(2) I use distilled water to prepare 1% light green, am I right? I can not 
counterstain the section well - or, possibly because the sections are still in 
red color.


2009-02-07 



TF 
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet