Accelerate to discover

Homepage>Discover>Timelapse analysis of cell migration using CQ1 confocal quantitative image cytometer

Dec 28, 2020

Radio-active sources have been used routinely for the preconditioning in humanized mouse models, but safety issues have...

EV imaging series: Using ONI super-resolution to characterize single-EVs

Dec 23, 2020

To date, researchers commonly use flow-based characterization methods, fluorescence imaging techniques and electron...

Don’t Let Waste Anesthetic Gases Harm You!

Dec 21, 2020

Many projects have been devoted to the study of the correlation between anesthetics and Alzheimer’s disease....

Coming in spring 2021, meet the Cytek Aurora CS

Dec 16, 2020

Ever wanted to take your full spectrum panel from your Cytek Aurora or Northern Lights cytometer and sort? Soon, you...

Dec 30, 2020

Advances in Leukemia research using shear flow and Bioflux system

Dec 10, 2020

Leukemia is a rare cancer with many subtypes. The production of abnormal leukocytes create disruptions in the immune...

Do you have our CellRad benchtop irradiator? It’s the only one on the market!

Dec 8, 2020

The CellRad is a smaller, simpler, safer, and more cost effective alternative to radioisotope or high-powered X-ray...

Dosimetric characterization of an X-ray irradiator for use with cells

Dec 4, 2020

This study aims to characterize an X-ray irradiator for use with cells using its internal parallel-plate ionization...

Dec 30, 2020

Modeling multiple myeloma-Bone Marrow interactions using Synthecon rotating-wall vessels

Dec 2, 2020

Multiple myeloma develops primarily inside the bone marrow microenvironment, that confers pro-survival signals and drug...

Show all topics (10)

Timelapse analysis of cell migration using CQ1 confocal quantitative image cytometer

Sep 6, 2017

The scratch was created on the cultures of Fucci-HeLa cells. Mitomycin C (MMC) was added to the culture medium to interrupt the cell-division cycle then washed out. Time-lapse imaging was performed for three days.The scratch was infiltrated by the cells in G1 and S/G2/M phase in the control cultures, indicating that the scratch was infiltrated not only by cell migration but also by proliferation as well. On the other hand, most of the infiltrating cells were in S/G2/M phase in the MMC-treated culture, indicating that the scratch was filled mostly by cell migration.

Read more

Scientific paper

Application

Product news

Related technologies: Automated microscopy and image analysis

Get more info

Head of application support

Riccardo

Pasculli

+420 731 127 717

pasculli@accela.eu

Send Message

Brand profile

Yokogawa

Yokogawa is a leading provider of confocal quantitative live cell imaging platforms. Combining superior technology with engineering services, project management, and maintenance, Yokogawa delivers field proven operational efficiency, safety, quality, and reliability.

More info at:
https://www.yokogawa.com/solutions/products-platforms/life-science/high-content-analysis/cq1/