Optical Imaging Techniques in Cell Biology
by Guy
Cox CRC Press / Taylor & Francis
http://www.guycox.com/optical.htm
______________________________________________
Associate
Professor Guy Cox, MA, DPhil(Oxon)
Electron Microscope Unit, Madsen Building
F09,
University of Sydney, NSW
2006
______________________________________________
Phone +61 2 9351
3176 Fax +61 2 9351 7682
Mobile 0413 281
861
______________________________________________
http://www.guycox.net
I
tend to agree with Dick here, The pinhole array solutions while less
"mature" than the spinning disk confocals work very well. We have had a
Yokagawa head for ages, and the limitation to a 1.4NA objective was
significant. About a year ago we bought a Prairie swept field array
scanning confocal. It allows multiple pinholes or slits sizes (7)
depending on your specimen and optics used. It works very well
indeed, and in our hands is more flexible than the Yokogawa head. Its
important to note that the yokogawa head I have is very old and there have been
many advances. However without rapid and simple changing of pinhole size
(as is possible with the Prairie or Visitech solutions) your image will be
compromised when NA is changed.
S.
Simon
C. Watkins Ph.D, FRCPath
Professor
and Vice Chair, Cell Biology and Physiology
Professor,
Immunology
Director,
Center for Biologic Imaging
BSTS
225, University of Pittsburgh
3500
Terrace St.
Pittsburgh
PA 15261
Tel:
412-352-2277
Fax:412-648-2797
URL:
http://www.cbi.pitt.edu
From: Confocal Microscopy
List [mailto:[hidden email]] On Behalf Of RICHARD
BURRY
Sent: Tuesday, February 10, 2009 3:20 PM
To:
[hidden email]
Subject: Re: Zeiss
SD
Fred
We have a Visitech
Infinity3 2D array scanning confocal. It is based on the same principle as
the spinning disk but use an array of pin holes. This confocal
allows seven different sizes of pin holes with diameter from 10
um to 60 um. Our experience is that is gives great performance with a
Hamamatsu EM13. With the 100x 1.4 N.A. the optimal pin hole is 30 um but
at 60 um the optical section thickness is a little more than a micron but the
intensity is great for even weak fluorescence.
Dick
-----
Original Message -----
From: Fred Mast <[hidden email]>
Date:
Tuesday, February 10, 2009 2:12 pm
Subject: Re: Zeiss SD
To:
[hidden email]
> Does the CSU-X1
allow you to change the disks? I'm still waiting for a spinning-disk unit
that is actually designed for live-cell imaging. The previous Yokogawa
units were optimized for 100x 1,4 NA oil objectives if I'm not mistaken.
Even with relatively thin samples (cultured cells), you're still
introducing spherical aberration... By comparison, has anyone else looked
at the technology being developed in Raphael Yuste's laboratory? They have
combined multiphoton LSM with spatial light modulation technology to
effectively "scan" an entire field at once. I'm not an expert in this but
in my opinion if you could make it fast enough this seems like a better
option to me (they report 60Hz calcium ion imaging). You can check it out
here (under the SLM Microscopy section):
>
Fred
D. Mast |
Richard W. Burry, Ph.D.
Department of Neuroscience, College of Medicine
Campus Microscopy and
Imaging Facility, Director
The Ohio State University
Associate Editor,
Journal of Histochemistry and Cytochemistry
277 Biomedical Research Tower
460 West Twelfth Avenue
Columbus, Ohio 43210
Voice
614.292.2814 Cell 614.638.3345 Fax
614.247.8849
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