
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.
Learn about the transformative power of NGS
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A deep dive into the cells' morphological and functional differences
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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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The revolutionary MACSima™ Platform streamlines your spatial biology research from end to end, reducing experimental workload and generating impactful data in no time. At its core is the fully automated MACSima™ System, which utilizes fluorescence ...
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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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