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<DIV style="FONT: 10pt arial">----- Original Message -----
<DIV style="BACKGROUND: #e4e4e4; font-color: black"><B>From:</B> <A
title=mparker@epl-inc.com href="mailto:mparker@epl-inc.com">Mary Parker</A>
</DIV>
<DIV><B>To:</B> <A title=histonet@pathology.swmed.edu.com
href="mailto:histonet@pathology.swmed.edu.com">histonet@pathology.swmed.edu.com</A>
</DIV>
<DIV><B>Sent:</B> Monday, September 22, 2003 8:03 AM</DIV>
<DIV><B>Subject:</B> Brain Tissue in Buffer</DIV></DIV>
<DIV><BR></DIV>
<DIV><FONT face=Arial size=2>If anyone has any experience about how to
successfully process and microtome serial sections of rat brain tissue that was
perfused, then stored in buffer solution for approx one year in the
refrigerator...please help! We were given this tissue by an outside investigator
and are having a miserable time of it.</FONT></DIV>
<DIV><FONT face=Arial size=2>I need all the information I can gather about
tissue stored in buffer for an extended period of time.</FONT></DIV>
<DIV><FONT face=Arial size=2>Is it hopeless?</FONT></DIV>
<DIV><FONT face=Arial size=2>Thanks</FONT></DIV>
<DIV><FONT face=Arial size=2></FONT> </DIV>
<DIV><FONT face=Arial size=2></FONT> </DIV>
<DIV><FONT face=Arial size=2>Mary Parker, H.T., A.S.C.P.<BR>Histology
Manager<BR>EPL, Inc.<BR>P.O. Box 12766<BR>RTP, N.C. 27709<BR>(919)
998-9407</FONT></DIV></BODY></HTML>