Re: Sectioning Problems with a sliding microtome
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From: | Alan Bright <Bright@dial.pipex.com> (by way of histonet) |
To: | histonet <histonet@magicnet.net> |
Reply-To: | |
Content-Type: | text/plain; charset="us-ascii" |
Dear Joyce,
Hacker Instruments should be able to assist you, they can be contacted on:
Tel. (973) 226-8450 or 1-800-4-HACKER
Fax. (973) 808-8281
e-mail: HACKERLAB@AOL.COM
++++++++++++++++++++++++++++++++++++++++++++++++++++++++
-----Original Message-----
From: Joyce Bousquet <jjbous@diacrin.com>
To: Histonet@pathology.swmed.edu <Histonet@pathology.swmed.edu>
Date: Thursday, January 07, 1999 07:52
Subject: Sectioning Problems with a sliding microtome
>Dear Mr. Lindsay Smart
>
> Thank you for responding to my question. When I purchased the
microtome
>I explained our application to our local Leica Rep and it was recommended
>that I use a Freezing Platform from a company in Boston called Brain
>Research Labs. I also visited other local Labs sectioning rat brains on
the
>sliding microtome and they were also using the freezing platforms from
Brain
>Research Labs. I have no knowledge of a peltier system or Frigimobil
>system. Could you elaborate on these?
>
>Thanks
>Joyce Bousquet
>Diacrin, Inc.
>Boston, MA
>
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