1993
DOI: 10.1016/s0301-4770(08)60566-7
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Chapter 6 Emerging Techniques: Enzyme-Linked Immunosorbent Assay (ELISA) as Alternatives to Chromatographic Methods

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“…Immunochemical methods have been developed for the determination of several mycotoxins including the aflatoxins, ochratoxin A, cyclopiazonic acid, rubratoxin, zearalanone, sterigmatocystin, and various trichothecenes (Chu, 1986;Ward et al, 1993 (PAb) against the fumonisins from the splenic lyphocytes of mice immunized with a FB 1 -cholera toxin conjugate. A MAb-based competitive direct enzymelinked immunosorbent assay (CD-ELISA) was developed, whereby FB 1 -horseradish peroxidase conjugate and free FB 1 competed for antibody binding sites immobilized on microtiter plates (Ascona-Olivera et al, 1992b).…”
Section: Introductionmentioning
confidence: 99%
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“…Immunochemical methods have been developed for the determination of several mycotoxins including the aflatoxins, ochratoxin A, cyclopiazonic acid, rubratoxin, zearalanone, sterigmatocystin, and various trichothecenes (Chu, 1986;Ward et al, 1993 (PAb) against the fumonisins from the splenic lyphocytes of mice immunized with a FB 1 -cholera toxin conjugate. A MAb-based competitive direct enzymelinked immunosorbent assay (CD-ELISA) was developed, whereby FB 1 -horseradish peroxidase conjugate and free FB 1 competed for antibody binding sites immobilized on microtiter plates (Ascona-Olivera et al, 1992b).…”
Section: Introductionmentioning
confidence: 99%
“…Immunochemical techniques for the determination of mycotoxins are generally rapid, matrix independent, and easy to apply in both the laboratory and field environments, exhibiting comparable sensitivity and higher selectivity characteristics than corresponding chromatographic methods (Chu, 1986;Ward et al, 1993). Immunochemical methods have been developed for the determination of several mycotoxins including the aflatoxins, ochratoxin A, cyclopiazonic acid, rubratoxin, zearalanone, sterigmatocystin, and various trichothecenes (Chu, 1986;Ward et al, 1993 (PAb) against the fumonisins from the splenic lyphocytes of mice immunized with a FB 1 -cholera toxin conjugate. A MAb-based competitive direct enzymelinked immunosorbent assay (CD-ELISA) was developed, whereby FB 1 -horseradish peroxidase conjugate and free FB 1 competed for antibody binding sites immobilized on microtiter plates (Ascona-Olivera et al, 1992b).…”
Section: Introductionmentioning
confidence: 99%