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.
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Super Resolution
Optimize results with the CSU-W1 SoRa Confocal Scanner.
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Wide Field of View
Improve efficiency with the CSU-W1 Confocal Scanner.
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High Speed
Get next level turnarounds with the CSU-X1 Confocal Scanner.
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Uniformizer
A flat-top beam shaper option for CSU-W1.
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 |
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| 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 |
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| Rotation position trigger signal |
External signal output possible | None*2 | ||||
| Filters | EX | Option | ||||
| DM | Option (up to 3 filters) | Option (1 filter) |
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| EM | Option (up to 10 filters with filter wheel) |
Option (up to 12 filters with filter wheel) |
Option (1 filter) |
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| Addition or exchange of filters |
At user site : DM block and filters (EX, EM.) At Yokogawa factory : DM |
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| *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
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Microscopy Techniques, Advances in Biochemical Engineering / Biotechnology Vol.95 |
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Confocal Microscopy for Biologists |
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Live Cell Imaging, A Laboratory Manual |
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Handbook of Biological Confocal Microscopy, 3rd Edition |
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VideoMicroscopy, The Fundamentals ISBN: 0-306-45531-5
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Direct-View High-Speed Confocal Scanner: The CSU-10, Chapter 2: Cell Biological Applications of Confocal Microscopy (Methods in Cell Biology) |
Publication List

Resources
First annual Yokogawa CSU Spinning Disk Image Competition at MBL 2023
Comparison between CSU and conventional LSM in 4D movies.
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.
Faster, Brighter, and More Versatile Confocal Scanner Unit
Downloads
Videos
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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