Life Science

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

Closing in on Neuronal Circuit Dynamics through High-speed, fMCI.

New Era in Manmmalian Genetics Research: To utilize the same embryo after long-time 3D observation!

Getting Closer to “Plant Cell World”with High-speed Live Imaging and Image Information Processing.

Spinning Disk Confocal Microscopy for Quantitative Imaging and Multi-Point Fluorescence Fluctuation Spectroscopy.

On-site manipulation of protein activities: Understanding intricate cell signaling pathways.

Use of the spinning disk confocal at the Harvard Medical School microscopy core.

The CV8000 nuclear translocation analysis software enables the analysis of changes in the localization of signal molecules that transfer between cytoplasm and nuclei, such as proteins. The following is an example of the translocation analysis of NFκB, a transcription factor.

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.

CV1000 clears the hurdle in Live Cell Imaging
All-in-one Live cell imaging solution

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.

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.

• Colony Formation
• Scratch Wound
• Cytotoxicity
• Neurite Outgrowth
• Co-culture Analysis
• Cell Tracking

Faster, Brighter, and More Versatile Confocal Scanner Unit

Welcome to The New World of High Content Analysis
High-throughput Cytological Discovery System

Cell clusters are directly measured with high-throughput 3D imaging Confocal Quantitative Image Cytometer

Wide and Clear
Confocal Scanner Unit

List of Selected Publications : CSU-W1

List of Selected Publications : CQ1

List of Selected Publications : CSU-X1

List of Selected Publications : CV8000, CV7000, CV6000

This "Tutorial" provides overview of this software, from installation through data analysis.

In this tutorial, a method for analyzing ramified structure, using CellPathfinder, for the analysis of the vascular endothelial cell angiogenesis function will be explained.

In this tutorial, a method for analyzing ramified structure, using CellPathfinder, for the analysis of the vascular endothelial cell angiogenesis function will be explained.

In this tutorial, spheroid diameter and cell (nuclei) count within the spheroid will be analyzed.

In this tutorial, we will learn how to perform time-lapse analysis of objects with little movement using CellPathfinder, through calcium imaging of iPS cell-derived cardiomyocytes.

In this tutorial, we will identify the cell cycles G1-phase, G2/M-phase, etc. using the intranuclear DNA content.

In this tutorial, image analysis of collapsing stress fibers will be performed, and concentration-dependence curves will be drawn for quantitative evaluation.

In this tutorial, we will observe the change in number and length of neurites due to nerve growth factor (NGF) stimulation in PC12 cells.

In this tutorial, intranuclear and intracytoplasmic NFκB will be measured and their ratios calculated, and a dose-response curve will be created.

In this tutorial, we will learn how to perform cell tracking with CellPathfinder through the analysis of test images.

In this tutorial, using images of zebrafish whose blood vessels are labeled with EGFP, tiling of the images and recognition of blood vessels within an arbitrary region will be explained.