Journal of Immunoassay · 1988 · 29 citations · 28 references
Life SciencesBiochemistryMolecular BiologyImmunotechnologyMonoclonal AntibodiesProtein BiochemistryAntibody CharacterizationAntibody-antigen RecognitionEnzyme CharacterizationEnzyme-linked Immunosorbent AssayHybridoma TechnologyPlasma ProteinsApolipoprotein QuantificationBiomolecular Binding AffinityCompetitive Enzyme-linked Immunosorbent AssayImmunoassay MethodologyImmunoassays For ApolipoproteinsMonoclonal Antibody RecognitionPolyclonal Antibodies
This study describes the development of an enzyme-linked immunosorbent assay for human apolipoprotein E (apo E). A mouse monoclonal IgG1 antibody named E01 against apolipoprotein E was selected from five antibodies secreted by hybridomas. This antibody had a high affinity for apo E [K = 1.2 x 10(7) L.M-1 for purified apo E and K = 1.05 x 10(7) L.M-1 for native apo E in very low density lipoproteins) in liquid phase and recognized every isoform of apo E but not other proteins in VLDL. Competition experiments with 125I apo E showed that its binding affinity for the E in every density class (VLDL, HDL, LDL) and in serum was the same. This antibody was used for the quantification of human apo E in serum by enzyme linked immunoassay. E01 was coated on microtiter plates and a polyclonal peroxidase-conjugate was used as second antibody. A good correlation was observed between the values obtained for apo E using both monoclonal and polyclonal antibodies.
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Continuous cultures of fused cells secreting antibody of predefined specificity
Georges Köhler, César Milstein · Nature · 1975 · 17.2K citations
Pharmacy, Cell Biology, Immunology +11