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Fri, 27 Jan 1995 16:16:18 -0500 |
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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]>
>To: Multiple recipients of list CONFOCAL <[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 |
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> |_________________________________________________|
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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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