
Flow Cytometry can be used to collect a multitude of information from cell populations, such as size, morphology, complexity, phenotype and function. Likewise, a diverse variety of reagents are available for your specific flow cytometry application. For instance, membrane impermeant DNA-intercalating dyes such as 7-AAD and propidium iodide (PI) are excluded from live cells, making them common tools in assessing cell health and cell viability. DAPI, another common dye, stains the nuclei of both live and fixed cells. In the analysis of specific cellular markers, fluorescent molecules are commonly used. Fluorescein/FITC, APC, cyanine, PE, and TRITC are some of the most well known, although new brands continually become available. These fluorophores can be found conjugated to secondary antibodies or other molecules such as Protein A, Protein G, or streptavidin. Protein A and G bind to immunoglobulins while streptavidin binds to biotin-conjugated antibodies. Taking advantage of multiple dyes allows for the multiplexing and simultaneous measurements of multiple analytes. Other flow cytometry reagents include standards for fluorophores, cell types, and for instrument calibration.
Researchers can now identify biomarkers with greater precision.
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From 4D proteomics to artificial intelligence
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Discover the beauty of standardized and automated flow cytometry
The MACSQuant® Analyzer 16 is an easy-to-use instrument designed for scalable and reliable flow cytometry assays. This includes features such as:
Full workflow automation: sample ...
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Introducing the LUNA-FX7™ - the automated cell counter that builds on the success of its predecessors. The LUNA-FX7™ is our most powerful cell counter to date, with unmatched cell counting accuracy, a maximum counting volume of 5 µL (10 times that of...
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To titrate the antibody, 1 x 10^6 splenocytes from C57BL/6 mice were stained with: FITC anti-CD4 Ab and PE anti-CD8a Ab in the presence of Zombie NIR in 100 µL PBS at 4C for 30 min.
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I need to measure transcription factor levels in single cells alongside surface phenotype. I use this buffer set to fix and permeabilize cells for intracellular flow cytometry staining of nuclear factors while preserving my surface marker signal.
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