CQ1 software is updated (R1.08.02). : Download
CellVoyager CQ1 enables 3D imaging and quantification of live cell clusters, such as spheroids within a 3D culture vessel, as they are, keeping the cells intact. CellVoyager CQ1 exports feature data in general formats readable by various third-party software for advanced data analysis. It is possible to construct a fully customized CellVoyager CQ1-based system by integrating with external systems*1, via robot for culture dish handling.
CellVoyager CQ1 System Highlights
| Excitation laser wavelength | 405 nm, 488 nm, 561 nm, 640 nm |
| Illumination source | Laser |
| Objective lens | 2x to 60x (Dry, Phase contrast, Long working distance) |
| Camera | High-sensitivity sCMOS camera |
| Autofocus | Laser autofocus, Software autofocus |
| Software | CellPathfinder |
Enables measurement of spheroids, colonies, and tissue sections
- There is no need to remove cells from the culture dish, in contrast to traditional flow cytometry
- Nipkow spinning disk confocal technology allows high-speed yet gentle 3D image acquisition
- Rich feature extraction to facilitate sophisticated cellular image analysis
- Wide field of view and tiling capability enables easy imaging of large specimen
Enables analysis of time-lapse and live-cell
- High precision stage incubator and low phototoxicity of our confocal analyze time-lapse and live-cell.
- Max.20fps option for fast time lapse*1
High-quality image and similar operability to a traditional flow cytometer
- Feature data and statistical graphs displayed in real-time with image acquisition
- Usable, high-quality image as confocal microscope image.
- It is easy to trace back to the original image from a graph spot and make repetitive measurements
Open platform
- Connectable with external systems via handling robot*2
- Expandable to the integrated system as an image acquisition and quantification instrument
- FCS/CSV/ICE data format readable by third-party data analysis software
- A variety of cell cultures and sample dishes are applicable
Compact footprint, lightweight bench-top device; no need for a darkroom
| CQ1 | General fluorescent imaging | Flow cytometry | |
|---|---|---|---|
| Cell removal/suspension treatment | Not necessary | Not necessary | Necessary |
| Cell image confirmation | Possible | Possible | Not possible |
| Display feature data and graphs in real time with imaging | Possible | Depends on devices | Possible |
| 3D data measurement | Possible | Not possible | Not possible |
| Time-lapse | Possible | Not possible | Not possible |
*1 Option
*2 Contact to CQ1 partner for more information
CQ1 User Group Meeting: On-Demand Talks
Did you miss our last CQ1 User Group Meeting? Register for the on-demand talks!
Contents
1. Cell Biology of Virus Infections (Prof Dr. Yohei Yamauchi, ETH Zurich)
2. The new Insights into tumor-stroma Interactions in Brain Metastasis by confocal Microscopy and 3D Reconstruction (Dr. Lisa Sevenich, Georg-Speyer-Haus - Institute for Tumor Biology and Experimental Therapy)
3. High-resolution multiplex immunofluorescence confocal Imaging in Breast Cancer Biomarker Discovery (Stefan Florian, MD PhD, Charité Berlin)
4. Quantifying beta-cell Proliferation in pancreatic Islets by 3D Colocalization Analysis of confocal Images (Özlem Yavas, PhD, InSphero AG)
5. In-Vitro Drug Discovery Models NerveSim® and BrainSim® (Lise Harbom, PhD, AxoSim)
6. HCA3 and GPR84 – Two metabolite-sensing GPCRs with opposing Functions in innate Immune Cells (PD Dr. Claudia Stäubert, University Leipzig)
Details
Multiple functions fully integrated in a compact box
Compact design contains fully integrated multiple functions to offer easy-to-handle confocal imaging system, without a need for complicated system integration. You only need to set a sample and run the software. User-friendly interface and versatile functions support your measurement and analysis.
Principles of the Microlens-enhanced Nipkow Disk Scanning Technology
A Nipkow spinning disk containing about 20,000 pinholes and a subsidiary spinning disk containing the same number of microlenses to focus excitation laser light into each corresponding pinhole are mechanically fixed on a motor, and very rapidly rotated. As a result, a high-speed raster scan of the excitation lights on the specimen can be achieved. The pinhole and microlenses are arranged on each disk in our proprietary design to optimize the raster scan. Multi-beam scanning not only increases scanning speed but also results in significantly lower photobleaching and phototoxicity because multi-beam excitation needs only a low level of laser power on the specimen to fully excite fluorescence.
System integration with CellVoyager CQ1
Measurement Procedure
Analysis software (Option)
High content analysis system CellPathfinder*1 Click Here For More Info!
- Preset analysis menus for a variety of applications
- Flexible graph functions to display analysis results
- Direct link between chart and object imageMachine learning
Machine learning
Software learns the features of the sampleobjects collected by users.
3D analysis
Label-free analysis
DPC*2 function is a powerful tool to analyze unstained bright field samples.
*1 Optional software
*2 Digital phase contrast
Example of setup
| Item | Specifications |
|---|---|
| Optics | Microlens enhanced dual wide Nipkow disk confocal, Phase contrast (Optional add-on) |
| Laser/Filter | Laser : Choose 2-4 lasers from 405/488/561/640nm, 10-position Filter wheel (built-in) |
| Camera | sCMOS 2560×2160pixel, 16.6×14.0mm |
| Objective lens | Max.6 lenses (Dry: 2x, 4x, 10x, 20x, 40x Long working distance: 20x, 40x Phase contrast: 10x, 20x ) |
| Sample vessel | Microplate (6, 24, 96, 384 well), Slide glass, Cover glass chamber*1, Dish (35, 60mm*1) |
| XY stage | High-precision XY stage, designated resolution 0.1µm |
| Z focus | Electric Z motor, designated resolution 0.1µm |
| Autofocus | Laser autofocus, Software autofocus |
| Feature data | Number of cells/cellular granules, Intensity, Volume, Surface area, Area, Perimeter, Diameter, Sphericity, Circularity, etc |
| Data format | Measurement data format: Original format (CQ1 format, CV8000 format), captured image format (16bit TIFF - OME-TIFF format) Output image format: TIFF (16bit, 8bit), PNG, JPEG Output video format: WMV, MP4 Output numerical format: FCS, CSV, ICE |
| Workstation | Measurement and analysis workstation |
| Size/weight | Main unit : 600×400×298mm 38kg Utility box : 275×432×298mm 18kg |
| Environment | 15 - 30oC、20 - 70％RH No condensation |
| Power consumption | Main unit and Utility box : 100-240VAC 800VAmax, Workstation : 100-240VAC 650VAmax |
*1 Under development *2 Display is not included with CQ1 system
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Collaborator
De Novo Software
(product name: FCS Express Image Cytometry)
De Novo Software has been developing flow cytometer data analysis solutions since 1998. Our flagship product, FCS Express™, is world-renowned as a robust, and easy to use flow and image cytometry data analysis application. De Novo Software offers a dedicated image analysis and reporting package for Image Cytometry to improve your workflow and results while giving you access to single cell results evening with high content screening data. FCS Express Image cytometry is directly compatible with the Yokogawa CQ1 quantitative image cytometer through the .ICE file format which enables quick import, analysis, and reporting of your results in FCS Express.
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CellPathfinder
CellPathfinder is designed for our HCA systems, CQ1 and the CellVoyager series. From beginners to experts, the analysis software lets you quantify subtle physiological changes and even label-free samples with various graph options.
Resources
Cell clusters are directly measured with high-throughput 3D imaging Confocal Quantitative Image Cytometer
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.
Cell stage categorized using FucciTime lapse imaging of Fucci-added Hela cells was conducted over 48 hrs at 1 hr intervals. Gating was performed based on the mean intensities of 488 nm and 561 nm for each cell. They were categorized into four stages, and the cell count for each was calculated.
List of Selected Publications : CQ1
Downloads
Brochures
- CQ1 Bulletin (21.1 MB)
Videos
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.
In this webinar, Professor Jonny Sexton discusses a pipeline, developed in the Sexton lab, for the quantitative high-throughput image-based screening of SARS-CoV-2 infection to identify potential antiviral mechanisms and allow selection of appropriate drug combinations to treat COVID-19. This webinar presents evidence that morphological profiling can robustly identify new potential therapeutics against SARS-CoV-2 infection as well as drugs that potentially worsen COVID-19 outcomes.
News
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Press Release Dec 3, 2020 Yokogawa and InSphero Enter into Partnership Agreement
- Supporting drug development research through the use of HCA and three-dimensional culture models -
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