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February 2017

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Subject:
From:
Craig Brideau <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Wed, 15 Feb 2017 08:23:26 -0700
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Some dyes can be cleared from the cone with a bath in vinegar if you notice
any persistence. I have used this for nile red.

Craig

On Feb 15, 2017 7:59 AM, "Cammer, Michael" <[log in to unmask]>
wrote:

> *****
> To join, leave or search the confocal microscopy listserv, go to:
> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy
> Post images on http://www.imgur.com and include the link in your posting.
> *****
>
> We've done it.  With rhodamine dextran.  No problems.  Recommend keeping
> lens hydrated between samples.
>
> =========================================================================
>  Michael Cammer, Microscopy Core & Skirball Institute, NYU Langone Medical
> Center
>          Cell:  914-309-3270     Office: Skirball 2nd Floor main office,
> back right
>             http://ocs.med.nyu.edu/microscopy &
> http://microscopynotes.com/
>
>
> -----Original Message-----
> From: Confocal Microscopy List [mailto:[log in to unmask]]
> On Behalf Of Claire Brown, Dr.
> Sent: Tuesday, February 14, 2017 10:20 PM
> To: [log in to unmask]
> Subject: Dye Solution with Dipping lens
>
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> *****
>
> I have a user who would like to do a multiphoton experiment with dipping
> lenses with rhodamine dye in the dipping solution.
> Would this be a problem for the dipping lenses?
> I would assume as long as the lens is cleaned well after use it should be
> fine.
>
> Anyone think otherwise?
>
> Sincerely,
>
> Claire
>
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