Re: RFP

From: Larry Arnold (lwarma@med.unc.edu)
Date: Fri Dec 14 2001 - 12:18:58 EST


Jack

I have one lab that has put DsRed2 in cells. They say it is brighter than
DsRed1 (analysis done on FACSCalibur with standard filters - use PE
channel) otherwise all I know is what Clonetech says about maturation rate,
toxicity and aggregation.

Larry

At 05:42 PM 12/13/2001, you wrote:
>Dear Larry:
>
>Our lab are very interested in the DsRed2 and needs some advice from
>experts.
>Do you have any new information about the DsReds? How is it going in your
>lab?
>
>Thanks a lot and Best Wishes,
>
>Jack
>
>----- Original Message -----
>From: Larry Arnold <lwarma@med.unc.edu>
>To: Cytometry Mailing List <cytometry@flowcyt.cyto.purdue.edu>
>Sent: Wednesday, November 28, 2001 10:32 AM
>Subject: Re: RFP
>
>
> >
> > You should be aware, if your'e not, that Clonetech now has DsRed2 which
> > apparently solves many of the problems with DsRed (now called DsRed1) -
> > faster maturation, low toxicity, low aggregation, brighter.  We have
> > several users working it up so I should know soon the results.
> >
> > Larry
> >
> > At 04:53 AM 11/28/2001, you wrote:
> >
> > >Dear Philippe,
> > >
> > >DsRed is a difficult beast to work with. Main problems are slow
>maturation
> > >and aggregation. We are submitting a paper on a tight link between
> > >aggregation (minimum is a dimer) and generation of a functional
> > >chromophore. I will be glad to share the results with you once we have
> > >feedback from the journal.
> > >
> > >ciao
> > >
> > >Saverio
> > >
> > >Saverio Alberti
> > >Head, Lab. of Experimental Oncology
> > >Department of Cell Biology and Oncology
> > >Consorzio Mario Negri Sud
> > >66030 Santa Maria Imbaro (Chieti), Italy
> > >Phone: (39-0872) 570.293
> > >FAX: (39-0872) 570.412
> > >E-mail: alberti@cmns.mnegri.it
> > >
> > >
> > >On Mon, 26 Nov 2001, Philippe Pognonec wrote:
> > >
> > > >
> > > > Dear all,
> > > > to track our transfected cells, we have to use a red fluorescent
> > > protein. We tried
> > > > pDS Red N1 (Clontech), but the signal obtain on our FAcSort is really
> > > bad (FL2 ), at
> > > > least as compared to what we get when we use pEGFP N1 (FL1).
> > > > Is anyone aware of a "better" red FP, that is efficiently excitable
> > > with the argon
> > > > laser, and displays a good and bright emission?
> > > > Philippe
> > > > ____________________________________________
> > > >
> > > > Philippe Pognonec, Ph.D.
> > > > Transcriptional Regulation and Differentiation
> > > > Centre de Biochimie
> > > > Parc Valrose
> > > > Universite de Nice
> > > > 06108 Nice cedex 2
> > > > France
> > > > Tel/fax: (33) 492 07 64 13
> > > > http://www.unice.fr/biochimie/u470/prog5us.htm
> > > > ____________________________________________
> > > >
> > > >
> > > >
> > > >
> > > >
> >
> > Larry W. Arnold, Ph.D.
> > Associate Professor
> > Director, Flow Cytometry Facility
> > Department of Microbiology and Immunology
> > Lineberger Comprehensive Cancer Center
> > CB# 7290
> > University of North Carolina at Chapel Hill
> > Chapel Hill, NC 27599
> > Phone: 919-966-1530
> > FAX: 919-962-8103
> >

Larry W. Arnold, Ph.D.
Associate Professor
Director, Flow Cytometry Facility
Department of Microbiology and Immunology
Lineberger Comprehensive Cancer Center
CB# 7290
University of North Carolina at Chapel Hill
Chapel Hill, NC 27599
Phone: 919-966-1530
FAX: 919-962-8103



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