CONFOCALMICROSCOPY Archives

March 2008

CONFOCALMICROSCOPY@LISTS.UMN.EDU
Options: Use Monospaced Font
Show Text Part by Default
Condense Mail Headers

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

Print Reply
Mime-Version:
1.0
Sender:
Confocal Microscopy List <[log in to unmask]>
Subject:
Re: 2-P of red fluorescent proteins
From:
Ann Haberman <[log in to unmask]>
Date:
Mon, 3 Mar 2008 14:22:21 -0500
In-Reply-To:
<D2762AE080674827A28B75D1A63ACB64@imager2>
Content-Type:
text/plain; charset="us-ascii" ; format="flowed"
Reply-To:
Confocal Microscopy List <[log in to unmask]>
Parts/Attachments:
text/plain (39 lines) 
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

I've heard good things about td-tomato, and am looking forward to 
trying it. My limited experience with mRFP has been frustrating as it 
seems to require a very long wavelength (>950 nm) at which most 
Ti:Saph don't typically have that much power.
-Ann

>Search the CONFOCAL archive at
>http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
>Hi all,
>Does anyone have experience with seeing DSRed or mCherry using a 
>Ti:Sa 2-P system?  If it doesn't work, what are the alternatives?
>
>Thanks,
>Carl
>
>Carl A. Boswell, Ph.D.
>Molecular and Cellular Biology
>University of Arizona
>520-954-7053
>FAX 520-621-3709


-- 

Ann Haberman, PhD
Department of Laboratory Medicine
Yale University School of Medicine
1 Gilbert  St.
TAC S541
New Haven, CT 06510

203-785-7349
203-785-5415 (fax)
[log in to unmask]

ATOM RSS1 RSS2