Our microscopy and life sciences solutions are designed to support applications from basic research to drug discovery to pre-clinical trials.
Yokogawa’s high content analysis systems and dual spinning disk confocal technologies are used in regenerative medicine, drug discovery, and precision medicine, providing high-speed and high-resolution live cell imaging.
As the pioneer in dual spinning disk technology, Yokogawa's confocal scanner units enable real-time live cell imaging technology, transforming optical microscopes.
Our high-content analysis systems utilize powerful analysis software to address a range of research applications from basic science to drug discovery screening.
December 9-11, 2018
Sales release : High Content Analysis Software CellPathfinder
Sales release : High-speed Super resolution Confocal Scanner CSU-W1 SoRa
2018 SLAS Europe
Sales release : High Content Data Management System CellLibrarian
February 3-7, 2018
|December||29,2017||Sales news : The Discontinuation of CellVoyagerTM CV7000S High-throughput Cytological Discovery System|
Sales release : CellVoyagerTMCV8000 High-throughput Cytological Discovery System
SLAS High-Content Screening Conference 2017
Poster presentation in 3D Cell Culture 2016, 19-21 April 2016, Konzerthaus Freiburg/Germany
Yokogawa Electric Corporation will present data obtained by our confocal image cytometer CQ1 in “3D Cell Culture 2016: How close to ‘in vivo’ can we get? Models, Application & Translation”. The poster will show the results of 3D live cell imaging and analysis of the migration and the network formation of HUVEC cells in a multilayered cell sheet. The results demonstrate that CQ1 is an excellent research tool in the field such as regenerative medicine and drug discovery screening.
*Data were provided from BioProcess Systems Engineering Lab., Dept.Biotech., Grad. Sch. Eng., Osaka University.
|February||10,2016||Yokogawa Concludes Distribution Agreement with Optec, LLC for Sale of Confocal Quantitative Image Cytometer CQ1 at the markets of OPTEC activity|
|October||01,2015||Sales release : Label-free Morphological Analysis Software CellActivision|
The most common conventional confocal microscopes use a single laser beam to scan a specimen, while the CSU scans the field of view with approximately 1,000 laser beams, by using microlens-enhanced Nipkow-disk scanning: in short, CSU can scan 1,000 times faster.
By using a disk containing microlens arrays in combination with the Nipkow disk, we have succeeded in dramatically improving the light efficiency and thus successfully made real-time confocal imaging of live cells possible.
The expanded and collimated laser beam illuminates the upper disk containing about 20,000 microlenses (microlens array disk). Each microlens focuses the laser beam onto its corresponding pinhole, thus, effectively increasing laser intensity through pinholes placed in the pinhole array disk (Nipkow disk).
With the microlens, backscattering of laser light at the surface of the pinhole disk can be significantly reduced, thus, dramatically increasing the signal to noise ratio (S/N) of confocal images.
About 1,000 laser beams passing through each of the pinholes fill the aperture of the objective lens, and are then focused on the focal plane. Fluorescence generated from the specimen is captured by the objective lens and focused back onto the pinhole disk, transmitted through the same holes to eliminate out-of-focus signals, deflected by the dichroic mirror located between microlens array disk and the Nipkow disk to split fluorescence signal from reflected laser, passed through emission filter and then focused into the image plane in the eyepiece or camera.
The microlens array disk and the Nipkow disk are physically fixed to each other and are rotated to scan the entire field of view at high speeds, thus, making it possible to view confocal fluorescent images in real-time through the eyepiece of the CSU head.
As compared to conventional single point scanning, multi beam scanning by the CSU requires a significantly low level of light intensity per unit area, which results in significantly reduced photo bleaching and phototoxicity in live cells.
1 line scan time＝1[ms]
Scan lines＝1000 [lines]
Disk Scanning by CSU
Rotation Speed＝10000 [rpm]=41.7[rps]
1÷( 41.7×30/360 )＝ 0.5 [ms]
Visualizing the cell behavioral basis of epithelial morphogenesis and epithelial cancer progression
Faster, Deeper, and Clearer -in vivo molecular imaging technology-
Discovering the Basic Principles of Life through the Live Imaging of C. elegans
Spinning Disk Confocal Microscopy for Quantitative Imaging and Multi-Point Fluorescence Fluctuation Spectroscopy.
Use of the spinning disk confocal at the Harvard Medical School microscopy core.
New Era in Manmmalian Genetics Research: To utilize the same embryo after long-time 3D observation!
On-site manipulation of protein activities: Understanding intricate cell signaling pathways.
Getting Closer to “Plant Cell World”with High-speed Live Imaging and Image Information Processing.
Closing in on Neuronal Circuit Dynamics through High-speed, fMCI.
The CQ1 confocal image acquisition mechanism with the distinctive CSU® unit has a function to sequentially acquire fine cell images along the Z-axis and capture information from the entire thickness of
cells which include heterogenic populations of various cell cycle stages. In addition, saved digital images can be useful for precise observation and analysis of spatial distribution of intracellular molecules.
The CQ1 capability to seamlessly analyze images and obtain data for things such as cell population statistics to individual cell morphology will provide benefits for both basic research and drug discovery
targetingM-cell cycle phase.
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