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Date: | Tue, 15 Apr 2008 07:23:12 -0400 |
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Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Dear Cameron, My group has experience with this. Let us communicate offline.
Badri Roysam
Professor, Department of Electrical, Computer and Systems Engineering
Associate Director, NSF Center for Subsurface Sensing & Imaging Systems (CenSSIS ERC)
Rensselaer Polytechnic Institute
110 8th Street, Troy, New York 12180-3590.
Office(JEC 7010): 518-276-8067, Lab(JEC 6308): 518-276-8207, Fax: 518-276-8715
Email: [log in to unmask], Web: http://www.ecse.rpi.edu/~roysam
----- Original Message -----
From: Nowell, Cameron [mailto:[log in to unmask]]
To: [log in to unmask]
Subject: Tracking Cell Division in 3D/4D
> Search the CONFOCAL archive at
> http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
> Hi List,
>
> Does anyone out there have any experience in tracking cell
> division in 3D? We want to be able to track the resulting daughter cells
> of T-cell division over a period of time (usually about 24 hours). We do
> not need to be able to do it in a live context (ie during acquisition),
> we just want to be able to analyse the movie after capture.
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> Thanks
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> Cam
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> Cameron Nowell
> Microscopy Research and Imaging Facility
> Cell Cycle and Development
> Peter MacCallum Cancer Centre
> 7 St Andrews Place
> East Melbourne, 3002
> Victoria AUSTRALIA
>
> Phone: +61396563759
> Fax: +61396561411
> Mobile: +61422882700
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