Laboratory Products
Premier Instrument in New Flow Cytometer Series
May 21 2009
Beckman Coulter, Inc has introduced the Gallios Flow Cytometry system, an instrument that delivers analytical excellence, coupling extraordinary sensitivity, resolution and dynamic range with high-speed data collection. The instrument’s unprecedented detection capabilities and easy-to-use software, combined with new dyes – some with proprietary tandem dye technology – facilitates superior performance of multi-color flow cytometry assays.
Developed for the research and biopharmaceutical markets, with input from a number of investigators, the multi-colour, multi-laser Gallios is the first in a series of key flow cytometry instrument, software and reagent releases that Beckman Coulter plans to announce this year.
A particular emphasis on optical and electronics design, combined with powerful automation and software tools, allows Gallios to greatly enhance the efficiency and analytical capabilities of flow cytometry laboratories. Patented electronics provide accurate and efficient digital signal processing at high event rates over a wide dynamic range of fluorescence intensities. These benefits are packaged in a compact analyser that delivers stable performance over long periods of time and across a wide range of operating temperatures.
The Gallios houses up to three highly reliable, solid-state lasers in standard red and blue, with violet available as an option. Easily interchanged optical filters facilitate detection of a variety of dyes and wavelengths.
An innovative forward-scatter detector provides up to three measurements of cell size and visualisation of particles down to 0.404 μm in diameter. A side-scatter detector incorporates an independently focused, high-performance photodiode with electronic attenuation.
Six fluorescence detectors provide simultaneous acquisition of up to six fluorescence signals. Up to four fluorescence detectors can be added to the system, enabling concurrent reading of up to 10 colours. Simultaneous measurements of integral, peak and width are available for all parameters, including scatter and fluorescence signals. A selection of up to 62 parameters can be processed per analysis, at acquisition rates of 25,000 events-per-second, with high yield. Three scalable configurations allow for the future addition of more lasers and fluorescence detectors as the applications for complex multi-colour flow cytometry expand.
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