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Радиоиммунный анализ (РИА)×Анализ методом проточной цитометрии×
ОбластьВетеринарияФармакология
СемействоProcess / pipelineProcess / pipeline
Год появления1959–19601976
Автор методаRosalyn Yalow and Solomon BersonLeonard Herzenberg
ТипQuantitative immunological assaycell analysis and sorting
Основополагающий источникYalow, 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 ↗
Другие названияRIA, radioisotope immunoassay, isotope immunoassay, radioligand assayFACS, fluorescence-activated cell sorting, cell analysis
Связанные13
СводкаRadioimmunoassay (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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  2. 2 Источники
  3. PUBLISHED
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ScholarGateСравнение методов: Radioimmunoassay · Flow Cytometry. Получено 2026-06-18 из https://scholargate.app/ru/compare