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Radioimmunoassay (RIA)×Analiza protočnom citometrijom×
PodručjeVeterinarska znanostFarmakologija
ObiteljProcess / pipelineProcess / pipeline
Godina nastanka1959–19601976
TvoracRosalyn Yalow and Solomon BersonLeonard Herzenberg
VrstaQuantitative immunological assaycell analysis and sorting
Temeljni izvorYalow, R. S., & Berson, S. A. (1960). Immunoassay of endogenous plasma insulin in man. Journal of Clinical Investigation, 39(7), 1157–1175. DOI ↗Herzenberg, 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 ↗
Drugi naziviRIA, radioisotope immunoassay, isotope immunoassay, radioligand assayFACS, fluorescence-activated cell sorting, cell analysis
Srodne13
SažetakRadioimmunoassay (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.Flow 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.
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ScholarGateUsporedite metode: Radioimmunoassay · Flow Cytometry. Preuzeto 2026-06-18 s https://scholargate.app/hr/compare