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Apskatiet izvēlētās metodes blakus; rindas, kas atšķiras, ir izceltas.

Imunenzimatisks tests ar antivielu piesaisti (ELISA)×Plūsmas citometrijas analīze×
NozareVeterinārzinātneFarmakoloģija
SaimeProcess / pipelineProcess / pipeline
Izcelsmes gads19711976
AutorsEva Engvall and Peter Perlmann; independent parallel development by Anton Schuurs and Bauke van WeemenLeonard Herzenberg
TipsQuantitative immunoassaycell analysis and sorting
PirmavotsEngvall, E., & Perlmann, P. (1971). Enzyme-linked immunosorbent assay (ELISA) quantitative assay of immunoglobulin G. Immunochemistry, 8(9), 871–874. 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 ↗
Citi nosaukumienzyme immunoassay, EIA, solid-phase enzyme immunoassay, ELISA testFACS, fluorescence-activated cell sorting, cell analysis
Saistītās23
KopsavilkumsELISA 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.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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ScholarGateSalīdzināt metodes: Enzyme-Linked Immunosorbent Assay (ELISA) · Flow Cytometry. Izgūts 2026-06-17 no https://scholargate.app/lv/compare