[Histonet] (no subject)
sgoebel <@t> xbiotech.com
sgoebel <@t> xbiotech.com
Wed May 12 10:21:38 CDT 2010
I know the histogel is pretty expensive (1500ish per kit), try ju plain agar powder and mix with water...it is super cheap that way. Happy spinning!! =)
Sarah Goebel, B.A., HT (ASCP)
H XBiotech USA Inc.
8201 East Ri -------- Original Message --------
Subject: Re: [Histonet] (no subject)
From: Kim Merriam <kmerriam2003 <@t> yahoo.com>
Date: Wed, May 12, 2010 7:49 am
To: "Cormier, Kathleen" <Kathleen.Cormier <@t> crl.com>
Cc: Histonet <histonet <@t> lists.utsouthwestern.edu>, sgoebel <@t> xbiotech.co m
Thanks for the tips everyone! I am going to order some aga (histogel) and use it! We are all very excited around here abo this, we have been pulling our hair out over these darn pellets.
Kim Merriam, MA, HT(ASCP)QIHC
Cambridge, MA
< _________________________________________________________________
From: "Cormier, Kathleen" <Kathleen.Cormier <@t> cr To: Kim Merri Subject: RE: [Histonet] (no subject)
Have you used Histogel? I have used it in the past (other pl employment) and on samples like yours. I just bought the gel, (not the whole unit, just the gel) scooped some out of the tube, placed
into a w took a transfer the tube/pellet on a then popped out the now solid baggie/paper) in a cassette. Works like Kathy
Kathy Cormier
Histology Manager
Charles River Laboratories
251 Ballardvale Street
Wilmin Ph: 781-222-6803
Fax: 978-988-8793
[1]kathleen.cormier <@t> crl.com
The Science will be get more informa Accelerating Drug Development. Exactly.
N confidential and m information. You must not disclose without Charles River's express written cons intended recipient you must not copy, distribute or the information contained in it for any purpose other th us. If you have received this message in error, please notify Charles River immediately, and delete it from your system.
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[mailto:[3]histonet-bounc Kim Merriam
Sent: Wednesda To: [4]histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] (no subje Good morning,
I am trying to make some nice FFPE cel lose a lot of cells along the way (espe the cells out of the tube). We are fixing spinning them down, adding 70% and spinning down again.&n that point, I am trying to scoop out the cells (with a weighing sco op) and wrap them in lens paper for processing. I am losing a lot of
Do take them was taught Anyone have any hot t Kim
Kim Merriam, MA, HT(ASCP)QIHC
Cambridge,
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