
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.
Outlook, obstacles, and new technologies advancing the field.
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From 4D proteomics to artificial intelligence
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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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Measure and assess your cell cultures with ease. Our Millicell® DCI Digital Cell Imager enables more efficient execution of the repetitive daily techniques associated with cell passaging. Quickly and objectively assess confluency, morphology, ...
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My goal was to examine dendritic cell populations to determine whether certain treatments resulted in more DC activation than others.
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In our lab, we test for paroxysmal nocturnal hemoglobinuria (PNH). Although there are antibodies for this application, the addition of FLAER has revolutionized the testing! It binds to all GPI-anchors, which are lost in PNH cells.
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