CONFOCALMICROSCOPY Archives

August 2004

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

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

Print Reply
Subject:
From:
Peter Van Osta <[log in to unmask]>
Reply To:
Date:
Wed, 11 Aug 2004 09:13:09 +0200
Content-Type:
text/plain
Parts/Attachments:
text/plain (39 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Hi,

In order to know what the appropriate sampling rate/magnification is,
you have to start at least from the Numerical Aperture of the Objective.
  Oversampling a bit (2.3 or 3), but beyond that it doesn't add detail
to the quality of the image.

Magnification as such is only a means to enlarge the image created by
the microsocpe, so we (or a camera) can distinguish the details of the
image created by the microscope.

For more information take a look at:

http://ourworld.compuserve.com/homepages/pvosta/pcrnyq.htm
and
http://www.ph.tn.tudelft.nl/People/young/manuscripts/QM/QM.html

Regards,

Peter

----------------------------------------------
Peter Van Osta

Director Imaging
MAIA SCIENTIFIC (formerly Union Biometrica NV)
Cipalstraat 3
B-2440 Geel, Belgium
Tel.: +32 (0)14 570 620
Mobile: +32 (0)497 228 725
Fax.: +32 (0)14 570 621
Email: [log in to unmask]
Website: www.maia-scientific.com
A Harvard Bioscience Company
----------------------------------------------

ATOM RSS1 RSS2