Spinning Disk Confocal CSU

What is Dual Spinning Disk Confocal Technology?

As the pioneer in dual-spinning disk confocal technology, we have revolutionized live-cell imaging in optical microscopy. The multi-beam scanning method offers not only high-speed imaging but also significantly reduced phototoxicity and photo bleaching, making our confocal scanner units the de facto standard tool for live-cell imaging.

Details

High-Speed, High Resolution Imaging

Yokogawa’s confocal scanners utilize advanced imaging technologies to enable researchers to achieve high-speed and high-resolution live cell imaging.

  • Fast time-lapse confocal images of living cells
  • Minimal phototoxicity and less photobleaching
  • Live-cell confocal fluorescence imaging capabilities
  • Stability during long-term and high-speed imaging
  • Facilitates quantitative analysis of huge amounts of data

Comparison of CSU Series

Model CSU-W1 CSU-X1
High-end Basic
Imaging Speed
(Max. fps)
200 2,000 360
Scanner Motor
Rotation Speed
(rpm)
1,500-4,000 1,500-10,000
(Variable)
1,800
(Fixed)*2
Recommended
camera
exposure time
5msec 0.5msec 33msec
Effective FOV 17x16mm 10x7mm
Disk unit Selectable up to
2 disks
Pinhole size : 50µm, 25µm
1 disk
Pinhole size : 50µm
Rotation
position trigger
signal
External signal output possible None*2
Filters EX Option
DM Option (up to 3 filters) Option
(1 filter)
EM Option
(up to 10 filters with
filter wheel)
Option
(up to 12 filters with
filter wheel)
Option
(1 filter)
Addition or
exchange of
filters
At user site : DM block and filters (EX, EM.)
At Yokogawa factory : DM
*1 option

Comparison between CSU and other confocal systems

Model CSU Conventional
Point-scan Confocal
Conventional
Slit-scan Confocal
Other spinning
disk Confocal
Epi-fluorescence
(Wide field)
Scan Type Microlens-enhanced
multi beam scan
Single beam scan Line Scan Disk scan (Multi beam or slit) None
Light Source Lasers Hg or Xenon arc lamp
Detector CCD, EMCCD PMT Line CCD CCD, EMCCD
Microscope Flexible Specific Flexible / Specific Flexible
Scan speed of
full-size image
2000fps ~1fps ~120fps (512X512) <200fps Any
Photo bleaching/
photo toxicity
Low Severe Low
Confocality High (X-Y-Z confocal) Modest
(Compromise
y-resolution)
Modest
(X-Y-Z confocal with pinhole,
Compromise y-resolution
with slit-scan)
None
Image Quality
(Background)
High Good S/N
(Low background)
High
(multiple averaging
necessary)
Modest Modest
(High background
with dim samples)
Low
(High background)

User labs

  • Ted Salmon Lab., Dept. of Biology, University of North Carolina, Chapel Hill
  • Waterman-Storer Lab., Laboratory of Cell and Tissue Morphodynamics (LCTM),NHLBI (Bethesda Campus)
  • Tim Mitchison Lab., Dept. of Systems Biology, Harvard Medical School
  • Scholey Lab., Dept. of Cell and Computational Biology, University of California, Davis
  • The Vale Lab., Dept. of Cellular and Molecular Pharmacology, University of California, San Francisco
  • The Wadsworth Lab., Biology Dept., University of Massachusetts, Amherst
  • The Kiehart Lab., Dept. of Biology, Duke University
  • HSC Core Facilities School of Medicine, University of Utah
  • Indiana Center for Biological Microscopy, Indiana University Medical Center
  • Ehlers Laboratory - Department of Neurobiology, Duke University
  • Bob Goldstein Lab., University of North Carolina Chapel Hill
  • Andrew Matus Lab., at Friedrich Miescher Institute for Biomedical Research
  • Laboratory of Developmental Dynamics,Graduate School of Life Sciences, Tohoku University
  • Zena Werb Lab., Anatomy, University of California San Francisco
  • Satoshi Nishimura Lab., Dept. of Cardiovascular Medicine, the University of Tokyo
  • Oshima Lab., Graduate School of Interdisciplinary Information Studies,The Univ. of Tokyo
  • The Huser research group at UC Davis
  • Nakano Lab., Graduate School of Science, University of Tokyo

Sites and Textbooks

1) Microscopy & Imaging Resources on the WWW

Complete list of all aspects of microscopy and imaging, by Douglas W. Cromey From Cellular Imaging Core of Southwest Environmental Health Sciences Center, University of Arizona College of Pharmacy, University of Arizona

 

2) The Centro de Biologia Molecular “Severo Ochoa” (CBMSO)

Contains links to general information, microscopy laboratories, publications, courses and meetings, societies, images. Especially useful for finding microscopy workshops.

 

3) The Cell Imaging Facility, a part of the University of Utah Health Science Center's Core Research Facilities Department

Good explanation of CSU-Disk scanning confocal system by Chris Rodesch

 

4) Molecular Expressions Website

Run by National High Magnetic Field Laboratory, Florida State University.
One of Web's largest collections of excellent optical microscopy images, and quite thorough information on all types of microscopy.
Interactive Java Tutorials sponsored by Nikon (Nikon MicroscopyU) and Olympus(Olympus Microscopy Resource Center) are extremely useful to learn not only confocal but all kinds of microscopies, and related technologies.

 

Life Science Textbooks

Microscopy Techniques, Advances in Biochemical Engineering / Biotechnology Vol.95
Serial Editor T. Scheper, Volume Editor J. Rietdorf, Springer(2005)
ISBN-10 3-540-23698-8

Confocal Microscopy for Biologists
Edited by Alan R.Hibbs,Kluwer Academic / Plenum Publishers(2004)
ISBN:0-306-48468-4(hardback) 0-306-48565-6(e-Book)

Live Cell Imaging, A Laboratory Manual
Edited by Robert D. Goldman & David L. Spector. 2nd Edition,Cold Spring Harbor Laboratory Press (2010)
ISBN:0-87969-893-4(pbk), ISBN 0-87969-892-6(hardcover)

Handbook of Biological Confocal Microscopy, 3rd Edition
Edited by James B. Pawley, Springer(2006)

VideoMicroscopy, The Fundamentals
Shinya Inoue, Kenneth Spring, Second Edition Plenum Press. New York,(1997)

ISBN: 0-306-45531-5

Direct-View High-Speed Confocal Scanner: The CSU-10, Chapter 2: Cell Biological Applications of Confocal Microscopy (Methods in Cell Biology)
Shinya Inoue and Ted Inoue
Edited by Brian Matsumoto Academic Press
ISBN:0-12-580445-8 ; 2nd Rev (2002/12)

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Resources

Overview:

First annual Yokogawa CSU Spinning Disk Image Competition at MBL 2023

Overview:

Comparison between CSU and conventional LSM in 4D movies.

Overview:

To investigate interactive dynamics of the intracellular structures and organelles in the stomatal movement through live imaging technique, a CSU system was used to capture 3-dimensional images (XYZN) and time-laps images (XYT) of guard cells.

Overview:

Faster, Brighter, and More Versatile Confocal Scanner Unit

Industries:
Yokogawa Technical Report
The World as Seen from Cells
(rd-te-r06002-001)
2.2 MB

Downloads

Videos

Overview:

YOKOGAWA proprietary Spinning Disk technology enables fast real-time confocal imaging for applications such as high-speed 3D and long-term live cell imaging. These quantifiable imaging analysis are essential tools for modern precision drug discovery.
 

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