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Enzyme-Linked Immunosorbent Assay (ELISA)×Radioimmunoassay (RIA)×
ÁreaCiências veterináriasCiências veterinárias
FamíliaProcess / pipelineProcess / pipeline
Ano de origem19711959–1960
Autor originalEva Engvall and Peter Perlmann; independent parallel development by Anton Schuurs and Bauke van WeemenRosalyn Yalow and Solomon Berson
TipoQuantitative immunoassayQuantitative immunological assay
Fonte seminalEngvall, E., & Perlmann, P. (1971). Enzyme-linked immunosorbent assay (ELISA) quantitative assay of immunoglobulin G. Immunochemistry, 8(9), 871–874. DOI ↗Yalow, R. S., & Berson, S. A. (1960). Immunoassay of endogenous plasma insulin in man. Journal of Clinical Investigation, 39(7), 1157–1175. DOI ↗
Outros nomesenzyme immunoassay, EIA, solid-phase enzyme immunoassay, ELISA testRIA, radioisotope immunoassay, isotope immunoassay, radioligand assay
Relacionados21
ResumoELISA is a plate-based immunoassay technique that detects and quantifies proteins, antibodies, antigens, hormones, and other analytes in biological samples. Widely used in veterinary science, medicine, and food safety, it exploits the specificity of antibody–antigen binding coupled to an enzyme-driven colorimetric signal to deliver sensitive, reproducible measurements across large sample batches.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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ScholarGateComparar métodos: Enzyme-Linked Immunosorbent Assay (ELISA) · Radioimmunoassay. Recuperado em 2026-06-18 de https://scholargate.app/pt/compare