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Date: | Wed, 12 Jan 2005 10:58:45 -0500 |
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Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Hi Urs,
I have an indirect answer to your posting. Without meaning to be
commercial, I wanted to point out that our "widefield confocal" MACROscope
technology makes it possible to scan large areas (22mm width strips up to
1 micron pixel resolution and 10mm width strips for submicron - down to
0.25 pixel resolution). Our systems are confocal and have optical
sectioning capabilites of these large areas. We can obtain images in
reflected, transmitted, fluorescence, phase contrast and hyperspectral
modes. Papers can be provided upon request. Some limited information can
be found on our current website - the submicron capability mentioned above
is new and that info is being updated shortly.
Glenn Smith
Biomedical Photometrics Inc.
www.confocal.com
[log in to unmask]
519.886.9013
On Sun, 9 Jan 2005 15:09:13 +0100, Urs Ziegler <[log in to unmask]>
wrote:
>Search the CONFOCAL archive at
>http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
>Dear All,
>
>we are scanning large areas in 3D using confocal microscopy. This is
>only possible by scanning individual smaller 3D volumes (tiled scanning
>using a motorized stage). Does anyone know of a software to assemble
>these individual tiled scans into one 3D volume data set. The individual
>scans are all partially overlapping!
>
>Thanks for all suggestions!
>
>Urs
>
>--
>Urs Ziegler, Ph.D.
>Institute of Anatomy
>University of Zurich
>Winterthurerstr. 190
>CH-8057 Zürich
>Switzerland
>
>Tel. +41 1 635 5355
>Fax. +41 1 635 5702
>e-mail: [log in to unmask]
>http://www.unizh.ch/anatom
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