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January 1995

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Confocal Microscopy List <[log in to unmask]>
Subject:
From:
Greg Erdos ICBR EM Core Lab Univers <[log in to unmask]>
Date:
Fri, 27 Jan 1995 16:16:18 -0500
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Confocal Microscopy List <[log in to unmask]>
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>From:  IN%"[log in to unmask]"  "Confocal Microscopy List"
>Subj:  Anti-fade agents
>
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>Date: Fri, 27 Jan 1995 15:11:21 -0400
>From: "John G. Aghajanian, Ph.D." <[log in to unmask]>
>Subject: Anti-fade agents
>Sender: Confocal Microscopy List <[log in to unmask]>
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>Hello folks,
>
>This may sound somewhat trivial but as one just starting out confocaling it
>is somewhat pertinent.  Is there a single anti-fade agent that works best
>for many/all fluorophores or are there certain anti-fade agents that work
>best with particular fluorophores? And, what are they?
>
>Thanks in advance,
>
> ___________________________________________________
> |                                                 |
> |   John G. Aghajanian, Ph.D.                     |
> |   Worcester Foundation for Experimental Biology |
> |   222 Maple Avenue                              |
> |   Shrewsbury, MA 01545-2737                     |
> |                                                 |
> |   Tel: 508 842-8921  ext. 147, 161              |
> |   Fax: 598 842-9632                             |
> |   [log in to unmask]                            |
> |                                                 |
> |_________________________________________________|
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        John,
                You should consult an article in J. Histochem Cytochem 41:
1833-1840, 1993 by Longin et al. who compared various anti-fade agents.
 
 
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     *  Greg Erdos             **                            *
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