Accelerate to discover
Related topics
STAT Protein Phosphorylation in CD4+ T Cells using the CellStream flow cytometer
Jan 21, 2021
Cytokine-induced protein phosphorylation is a key cell signaling event within the immune system that modulates diverse...
Introducing Cytek cFluor, 14 Colors Immunoprofiling Kit
Jan 19, 2021
Cytek cFluor Immunoprofiling Kit allows for the identification of helper T cells, cytotoxic T cells, B cells, NK cells...
A Glimpse on physiological monitoring for the in vivo SKYSCAN Systems
Jan 14, 2021
This past year has proven once again that in vivo imaging is an important aspect in the microCT world. For longitudinal...
Cytek full Spectrum flow Cytometry webinar: Part II – panel design and troubleshooting
Jan 11, 2021
In this session, we will continue to look at full spectrum flow cytometry and look at considerations for fluorescence...
CQ1 webinar : optimizing high-content imaging of 3D models for drug discovery
Jan 7, 2021
In vitro spheroid models are fast becoming the de facto standard for drug discovery applications, largely due to their...
IncuCyte for in-vitro analysis of SARS-CoV-2 vaccine candidate
Jan 4, 2021
Watch this video to learn how researcher at Humane Genomics are utilizing the Incucyte platform for the in-vitro...
High gain mode now available on the Amnis ImageStreamX Mk II
Dec 31, 2020
Increase camera gain during data acquisition and dramatically increase photonic sensitivity with High Gain mode, a new...
Cesium-137 versus X-ray irradiation preconditioning in immunodeficient NOG mice
Dec 28, 2020
Radio-active sources have been used routinely for the preconditioning in humanized mouse models, but safety issues have...
Nov 14, 2016
There are two approaches to studying cell proliferation. One is to observe changes in the cell cycle; the other is to follow the number of cell divisions over a period of time. In the first method, at the most, three cell divisions can be followed. We can measure proliferation through absolute cell counts or with a dye, such as CFSE. When cells labeled with CFSE divide, the dye is partitioned equally between daughter cells and we can measure the loss of CFSE fluorescence over time as the dye is continuously diluted. The mean fluorescence intensity (MFI) of the dye was also plotted with cell concentration over time to show the inverse relationship between the two. This type of assay is often used to look at changes in T lymphocyte activation.
Related technologies: Conventional flow cytometry
Get more info
Brand profile
Agilent provides xCELLigence impedance-based, label-free, real time cell analysis system and NovoCyte flow cytometers.
More info at:
www.aceabio.com
BioFocus newsletter
Register to receive Brand new technology development, Important product updates, Interesting scientific events and more!
BioTech a.s. © 2014
Designed & developed by imagineit
Technologies
