1991
DOI: 10.1016/0022-1759(91)90152-6
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An appraisal of polystyrene- (ELISA) and nitrocellulose-based (ELIFA) enzyme immunoassay systems using monoclonal antibodies reactive toward antigenically distinct forms of human C-reactive protein

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Cited by 29 publications
(14 citation statements)
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“…Residual sera from the hormonal assays were used to perform the initial CRP tests. An enzyme-linked immunoflow assay (ELIFA) was performed, with a minimum detection limit of 1 mg/l, in the Department of Cell, Molecular, and Structural Biology at NWU [30]. The second set of female cohort sera was derived from 21 pre-RA and 84 CN subjects, who constituted the remaining women eligible for inclusion in study and who had available stored (-70°C) sera in CLUE I (fig.…”
Section: Methodsmentioning
confidence: 99%
“…Residual sera from the hormonal assays were used to perform the initial CRP tests. An enzyme-linked immunoflow assay (ELIFA) was performed, with a minimum detection limit of 1 mg/l, in the Department of Cell, Molecular, and Structural Biology at NWU [30]. The second set of female cohort sera was derived from 21 pre-RA and 84 CN subjects, who constituted the remaining women eligible for inclusion in study and who had available stored (-70°C) sera in CLUE I (fig.…”
Section: Methodsmentioning
confidence: 99%
“…(b) Amino acid composition analysis (Analytical Biotechnology Services, Boston, MA) showed that r m CRP contained the same number of amino acid residues per mol of protein as mCRP with the exception of 11 alanine residues per mol of r m CRP compared with 9 per mol of mCRP, no cysteine residues in r m CRP versus 2 cysteine residues per mol of mCRP and 3 methionine residues per mol of r m CRP compared with 2 in mCRP, corroborating the changes engineered in r m CRP. (20) react with the same specificity and affinity to mCRP, r m CRP (33), and acylated forms of r m CRP. Furthermore, preliminary experiments showed that, on a molar basis, mCRP and r m CRP and acylated forms of r m CRP produced similar delays in neutrophil apoptosis assessed by annexin V and acridine orange staining (see below).…”
mentioning
confidence: 99%
“…When proteins are adsorbed on material surfaces, some epitopes are masked, which reduces the binding of the corresponding antibodies [77][78][79]. Conversely, some internal protein epitopes may become exposed upon adsorption onto material surfaces, which increases the binding of the corresponding antibodies [80]. Monoclonal antibodies are therefore useful to determine the domain of interaction between proteins and material surfaces and to estimate the degree of unfolding of adsorbed proteins.…”
Section: Evidences Of Material-induced Protein Conformational Changesmentioning
confidence: 99%