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Analyse par cytométrie en flux×Radioimmunoassay (RIA)×
DomainePharmacologieSciences vétérinaires
FamilleProcess / pipelineProcess / pipeline
Année d'origine19761959–1960
Auteur d'origineLeonard HerzenbergRosalyn Yalow and Solomon Berson
Typecell analysis and sortingQuantitative immunological assay
Source fondatriceHerzenberg, L. A., Parks, D., Sahaf, B., Perez, O., Roederer, M., & Herzenberg, L. A. (2002). The history and future of the fluorescence-activated cell sorter and flow cytometry: a view from Stanford. Clinical Chemistry, 48(10), 1819-1827. DOI ↗Yalow, R. S., & Berson, S. A. (1960). Immunoassay of endogenous plasma insulin in man. Journal of Clinical Investigation, 39(7), 1157–1175. DOI ↗
AliasFACS, fluorescence-activated cell sorting, cell analysisRIA, radioisotope immunoassay, isotope immunoassay, radioligand assay
Apparentées31
RésuméFlow cytometry is a laser-based technology for analyzing and sorting individual cells based on fluorescent markers. Developed by Leonard Herzenberg in the 1970s, flow cytometry enables rapid assessment of cell phenotype, drug effects on cell populations, and therapeutic cell characterization in immunology and hematology.Radioimmunoassay (RIA) is a highly sensitive, quantitative laboratory technique that measures the concentration of a specific antigen — such as a hormone, drug, or pathogen-derived protein — in a biological sample by exploiting competitive binding between a radiolabelled antigen and the sample antigen for a limited supply of specific antibody. Developed in the late 1950s, RIA is widely used in veterinary science, endocrinology, pharmacology, and clinical diagnostics.
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ScholarGateComparer des méthodes: Flow Cytometry · Radioimmunoassay. Consulté le 2026-06-19 sur https://scholargate.app/fr/compare