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NovoCyte Quanteon - when exceptional performance meets simplicity
Jun 21, 2018
NovoCyte Quanteon system is the answer for growing demands in modern flow-cytometry assays. With its four lasers (405,...
Real-time study of platelet formation under sheer-flow with Lumascope
Jun 18, 2018
Platelet formation was observed with Lumascope microscope in a uniform-sheer-flow biorector. Videos of the formation...
Early fetal sex determination using micro-volume of maternal plasma
Jun 16, 2018
A qPCR-based assay, SneakPeek Early Gender Test (Gateway Genomics) has been developed to determine fetal sex as early...
3R Compliant drug development studies
Jun 8, 2018
In preclinical imaging, magnetic resonance imaging (MRI) can be an attractive alternative to researchers who have...
Kinase study of cytotoxicity voted paper of the year.
Jun 6, 2018
Society of Toxicology voted a xCELLigence based paper the Paper of the Year. The study of cytotoxicity was done using...
Heterodimeric compounds with dual-targeting active against both HIV and tuberculosis.
Jun 4, 2018
Search for dual action drugs against both HIV and Tuberculosis has lead to the creation of heterodimeric compounds with...
Mutual destruction of deep Lung tumor tissues by nanodrug‐conjugated and CQ1 imaging cytometer
Jun 1, 2018
Lung cancer is a highly malignant tumor, and targeted delivery of anti‐cancer drugs to deep lung tumor tissue remains a...
Method to quantify local force distribution within biomolecular systems
May 24, 2018
The journal Nano Letters has recently published the article “Quantifying Local Molecular Tension Using Intercalated DNA...
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
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ACEA manufactures xCELLigence impedance-based, label-free, real time cell analysis system and NovoCyte flow cytometers.
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www.aceabio.com
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