Widefield Confocal Scanner Unit CSU-W1

Widefield Confocal Scanner Unit CSU-W1 is a confocal unit that enables confocal imaging when attached to an optical microscope. Utilizing a proprietary spinning-disk confocal design, it offers features ideal for live-cell imaging, including high-speed acquisition and low phototoxicity.
Compared to previous models, CSU-W1 delivers an improved field of view and image quality, and is available with a wide range of options—including support for NIR wavelengths, photostimulation, super-resolution imaging, and illumination uniformity. As a result, CSU-W1 is widely used across diverse research fields that continue to advance rapidly.
 

High-Speed Imaging with a Wide Field of View

  • Compared with conventional models, the enlarged spinning disk expands the field of view by up to four times.
  • Enables high-resolution observation that fully leverages wide-field, high-sensitivity cameras from various manufacturers

Higher Image Quality and Clarity

  • By increasing the spacing between pinholes on the pinhole array disk, crosstalk is reduced, enabling confocal imaging with minimal flare
  • Clear imaging is possible even deep inside thick samples

Versatility for a Wide Range of Research Applications

  • Selection of pinhole diameters allows configuration of a confocal system optimized for specific experiments
  • Motorized disk retraction from the optical path enables brightfield and phase-contrast observation
  • Supports simultaneous dual-camera imaging and split-field imaging with various two-wavelength combinations, such as G/R and C/Y
  • Fully motorized switching of all modes ensures simple and intuitive operation

Details

Wide

Widest FOV confocal! Provides 4 times wider FOV than the conventional model.

Widest FOV confocal

 

Clear

Newly designed disk unit offers much improved image quality. Due to significantly reduced pinhole crosstalk, CSU-W1 enables clear observation much deeper into thick samples.

Conventional model

XY MIP

XZ Slice

XY MIP:Conventional XZ Slice:Conventional

CSU-W1

XY MIP

XZ Slice

XY MIP:CSU-w1 XZ Slice:CSU-w1

Mouse ES cell colony
Fluorescent probe:  H2B-EGFP(Excitation:488nm) mCherry-MBD-NLS(Excitation: 561nm)
Objective lens:  60x silicone
Z-sections/stack:  100um(0.4m/251slices)
By courtesy of Jun Ueda, Ph.D. and Kazuo Yamagata, Ph.D., Center for Genetic Analysis of Biological Responses, The Research Institute for Microbial Diseases, Osaka University

Thin sample:Conventional,Thick sample:Conventional,Thick sample:CSU-W1

 

Flexible

Flexibly selectable functions to meet versatile applications.

High confocality pinhole (Optional Component)

In addition to our conventional 50um pinhole size, 25m pinhole size with higher confocality is available.
You can select either one or the both pinhole size, with easy-to-use motorized disk exchange mechanism.

Disk unit

New bright field through path (Standard)

New mechanism to move the disks out of the light path allows much easier projection of confocal and non-confocal images such as phase contrast.

Simultaneous dual color imaging mechanisms
(T2 and T3 Models)

CSU-W1 offers single camera split-view model, in addition to the dual camera model which are much improved from those for the CSU-X1. Thanks to the wide FOV, even the split-view offers 2 times wider image area than with older model. By using various dichroic mirrors, it is possible to select various dye-combinations for dual-color imaging*1 with both the two camera model and split-view model.

 

Basic Configurations

CSU-W1 offers selection from a total of three basic configurations, two pinhole sizes, options for near infrared observation and an external light path which is useful for versatile applications such as photo bleaching, while bright field light path is now a standard feature. All switching mechanisms in the CSU-W1 are fully motorized and thus ready for automated experiments.

Basic Configurations

CSU-W1 provides a total of three basic configurations for multi- color imaging; 1) Sequential imaging with one camera and a filter wheel, 2) Simultaneous two-color imaging with two cameras, and 3) Split-view two color imaging with one camera shared by 2 optical paths. All features are upgradable after installation.

Basic Configurations

Filter

Filter

Option

SoRa disk

Optical resolution has been improved by approximately 1.4x using a super-resolution technique based on spinning-disk confocal technology. Furthermore, a final resolution approximately twice that of the optical limit is realized through deconvolution.
Upgrading from the CSU-W1:CSU-W1 SoRa

Uniformizer

Most suitable option for CSU-W1 illumination uniformity. Uniform and efficient illumination of the entire wide field of view.

Near Infrared (NIR) Port

NIR port provides up to 785nm excitation capability to allow less-invasive deep imaging. The NIR laser is introduced via a dedicated optical fiber in the same way as visible lasers. It is possible to combine NIR and visible lasers within the CSU-W1 unit to allow simultaneous excitation.

External light path

External light path provides the direct path bypassing the disk s to microscope. Versatile applications such as photo activation are available by introducing an external light scanner through this port.

Lens switcher

Newly designed motorized lens switcher between 2 relay lenses i s useful for fitting CSU-W1 image size with various camera types, and also for easy magnification change without exchanging objective lenses.

Variable aperture

Variable aperture to change laser illumination area, and thus the imaging area by the CSU-W1, is useful to minimize laser damages in the specimen.

Selectable option

Option 1 Camera model 2 Camera model Split-view model
NIR port
External light path
Variable aperture N/A
Camera port lens Selectable from
0.83x, 1x
Selectable from
0.83x, 1x
(1 Camera)
Selectable from
0.83x, 1x
(2 Camera)
Selectable from
0.83x, 1x
Additional lens
to lens switcher
Selectable from 0.83x, 1x, 2x N/A

2 Camera model, 1 Camera model

2 Camera model, 1 Camera model

 

Split-view model

Split-view model

*1  2 Camera model  *2  2 Camera model and Split-view model
*3  1 Camera model and 2 Camera model 

 

Specifications

General Specifications
Model 1 camera model (T1) 2 camera model (T2) Split-view model(T3)
Confocal scanning method Microlens-enhanced dual spinning disk scanning
Spinning speed 1,500rpm - 4,000rpm Max200fps
External synchronization Scan-speed synchronization through pulse signals Input/output : TTL level 300Hz up to 800Hz
Disk unit Selectable up to 2 disks from 50um
(for high magnification)
and 25um(for low magnification)
Motorized switching
Bright field Motorized exchange between confocal and brightfield
Effective FOV 17×16mm
Excitation wavelength 405nm-785nm
Laser introduction Yokogawa's standard fiber*1 VIS Laser port (405-647nm)
【Option】NIR Laser port (685-785nm)
Observation wavelength 420nm-850nm
Dichroic mirror switching Motorized 3CH (Dichroic mirror block can be exchanged)
Emission filter wheel 10-position filter wheel
Filter sizeφ25mm
Switching speed*2 : 100msec max.(Standard mode) 40msec max.(High speed mode)
6-position filter wheel
Filter sizeφ25mm
Switching speed*2 : 100msec max.
External control RS-232C (CSU-X1 command upper compatible)
Microscope mount Yokogawa original
Camera adaptor C mount 1x (Variable magnification: 0.83x )
Light introduction port 【Option】Photo breach etc
Operating environment 15-30oC、20-75%RH No condensation
Power consumption Input : 100-240 VAC ±10% 50-60Hz 250VAmax
External dimension Main unit 480(W)x 327(D)x 252(H)mm 480(W)x 476(D)x 252(H)mm 374(W)x 425(D)x 252(H)mm
Power unit 225(W)x 378(D)x 152(H)mm
Weight Main unit 17kg 20.5kg 18kg
Power unit 5kg
Attachable microscope Olympus IX series, Nikon ECLIPSE Ti , Zeiss Axio Observer, Leica DMI series*3

*1 Each CSU-W1 head is optimized with its fiber at factory. Please inquire about fiber exchange if necessary.
*2 Adjacent position.
*3 Some microscopes/options could limit the FOV of CSU-W1 or connection with CSU-W1, please inquire.

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CSU-W1 Partners


Nikon

Nikon Instruments Inc.  
(North and South America)

Nikon Instruments Europe B.V.  
(Europe)

Nikon Corporation  
(Asia except for Japan)
 



 

Resources

Application Note
Overview:

Wide and Clear
Confocal Scanner Unit

Overview:

Long-term observation of mitosis by live-cell microscopy is required for uncovering the role of Cohesin on compartmentalized nuclear architecture which is linked to nuclear functions.
To perform long term observation of mitosis devices are needed that have low phototoxic effects on living cells and enable high speed imaging. By using the CSU W-1 confocal scanner unit for time lapse imaging entrance into mitosis, mitotic progression and exit can be examined.

Overview:

SU10 is a novel technology that enables the delivery of target substances directly into cells (nucleus or cytoplasm) using a "nano" pipette made of a glass capillary with an outer tip diameter of tens of nanometers.

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.

Yokogawa Technical Report
The World as Seen from Cells
(rd-te-r06002-001)
2.2 MB
Yokogawa Technical Report
Confocal Scanner Unit CSU-W1
(rd-te-n05601-002)
414 KB
Overview:

List of Selected Publications : CSU-W1

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.
 

Overview:

YOKOGAWA will contribute to technology evolution particularly in measurement and analytical tools to help build a world where researchers will increasingly focus on insightful interpretation of data, and advancing Life Science to benefit humanity.

Overview:

Over past 20 years, YOKOGAWA proprietary Spinning Disk Confocal technology has been widely used as an indispensable imaging tool among top researchers. The technology enables faster live-cell observation with clearer and less photo-bleaching imaging.

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