CONFOCALMICROSCOPY Archives

May 2005

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
"Mcnamara, George" <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Wed, 11 May 2005 17:45:49 -0700
Content-Type:
text/plain
Parts/Attachments:
text/plain (121 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Try direct email to either Rachel Errington ([log in to unmask]
<mailto:[log in to unmask]> ) or Paul Smith ([log in to unmask])
<mailto:[log in to unmask])> , or both.


                -----Original Message-----
                From:   simon watkins [mailto:[log in to unmask]]
                Sent:   Wednesday, May 11, 2005 1:42 PM
                To:     [log in to unmask]
                Subject:        Re: DRAQ-5 and tissue sections

                Search the CONFOCAL archive at
                http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

                Ok clare...and everyone else
                I love Drac 5
                We use it at 1:2000 dilution (no more concentrated!), and
mix it with the
                secondary antibody (it takes about 45 minutes to give very
clean very
                distinct nuclear staining at this dilution).  We mount in
aqueous mountants,
                (gelvatol).  Its very bright and beam stable (we don't use
antifades at
                all)..... the only problem is we don't seem to be able to
get in touch with
                the company that makes it right now... does anyone else have
this problem?
                Simon


                Simon C. Watkins Ph.D. FRC Path.
                Professor, Cell Biology and Physiology and Immunology
                Director Graduate Program in Cell Biology and Physiology
                Vice Chair, Cell Biology and Physiology
                Director Center for Biologic Imaging
                BSTS 225
                University of Pittsburgh
                3500 Terrace St.
                Pittsburgh PA 15261
                Tel:412-648-3051
                Fax:412-648-2797
                URL: http://www.cbi.pitt.edu

                -----Original Message-----
                From: Confocal Microscopy List
[mailto:[log in to unmask]] On
                Behalf Of Clare Waterman
                Sent: Wednesday, May 11, 2005 4:14 PM
                To: [log in to unmask]
                Subject: Re: DRAQ-5 and tissue sections

                Search the CONFOCAL archive at
                http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

                Ask simon Watkins at pitt.  He was discussing this recently
but I forget wha
                he said

                Clare M. Waterman-Storer, Ph.D.
                Associate Professor
                Laboratory for Cell Motility Studies
                Department of Cell Biology CB163
                The Scripps Research Institute
                10550 North Torrey Pines Road
                La Jolla CA, 92037 USA
                Office:  858-784-9764
                Lab:  858-784-9243
                Secretary (Lorraine Lathrop): 858-784-9964
                Fax:  858-784-9779
                Email:  [log in to unmask]

                -----Original Message-----
                From: Confocal Microscopy List
[mailto:[log in to unmask]] On
                Behalf Of Maher, Robert
                Sent: Wednesday, May 11, 2005 11:30 AM
                To: [log in to unmask]
                Subject: DRAQ-5 and tissue sections

                Search the CONFOCAL archive at
                http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

                Does anyone have any experience with labeling sections with
the nuclear
                probe DRAQ-5 (BioStatus Ltd.)?  I'm specifically interested
in the mounting
                medium chosen.  I labeled tissue sections with DRAQ-5 and
mounted the
                sections with ProLong Gold (Molecular Probes).  After a day
the staining is
                significantly decreased.  I've also mounted the sections in
water and
                glycerin and have had somewhat better success.  Any insight
would be
                appreciated.

                Robert Maher, Scientist
                Safety Sciences Michigan-Ann Arbor
                Pfizer Global Research and Development
                e-mail:  [log in to unmask]




                LEGAL NOTICE
                Unless expressly stated otherwise, this message is
confidential and may be
                privileged. It is intended for the addressee(s) only. Access
to this E-mail
                by anyone else is unauthorized. If you are not an addressee,
any disclosure
                or copying of the contents of this E-mail or any action
taken (or not taken)
                in reliance on it is unauthorized and may be unlawful. If
you are not an
                addressee, please inform the sender immediately.

ATOM RSS1 RSS2