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An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody.
An enzyme-linked immunosorbent assay (ELISA) test has been developed for measurement of heterophile antibody. The microtiter test utilizes a bovine erythrocyte monolayer as antigen and anti-human IgM antiserum conjugated with horseradish peroxidase to measure the degree of binding of the heterophile...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Yale Journal of Biology and Medicine
1982
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596542/ https://www.ncbi.nlm.nih.gov/pubmed/6763815 |
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author | Hsu, J. F. Evans, A. S. Niederman, J. C. Cenabre, L. C. |
author_facet | Hsu, J. F. Evans, A. S. Niederman, J. C. Cenabre, L. C. |
author_sort | Hsu, J. F. |
collection | PubMed |
description | An enzyme-linked immunosorbent assay (ELISA) test has been developed for measurement of heterophile antibody. The microtiter test utilizes a bovine erythrocyte monolayer as antigen and anti-human IgM antiserum conjugated with horseradish peroxidase to measure the degree of binding of the heterophile antibody in the test serum with the erythrocytes. A single serum dilution yields quantitative results when read in a spectrophotometer. The ELISA test showed a sensitivity comparable with the immune adherence hemagglutination assay (IAHA) and other heterophile tests, good reproducibility, and high specificity. |
format | Text |
id | pubmed-2596542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1982 |
publisher | Yale Journal of Biology and Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-25965422008-12-05 An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. Hsu, J. F. Evans, A. S. Niederman, J. C. Cenabre, L. C. Yale J Biol Med Research Article An enzyme-linked immunosorbent assay (ELISA) test has been developed for measurement of heterophile antibody. The microtiter test utilizes a bovine erythrocyte monolayer as antigen and anti-human IgM antiserum conjugated with horseradish peroxidase to measure the degree of binding of the heterophile antibody in the test serum with the erythrocytes. A single serum dilution yields quantitative results when read in a spectrophotometer. The ELISA test showed a sensitivity comparable with the immune adherence hemagglutination assay (IAHA) and other heterophile tests, good reproducibility, and high specificity. Yale Journal of Biology and Medicine 1982 /pmc/articles/PMC2596542/ /pubmed/6763815 Text en |
spellingShingle | Research Article Hsu, J. F. Evans, A. S. Niederman, J. C. Cenabre, L. C. An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. |
title | An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. |
title_full | An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. |
title_fullStr | An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. |
title_full_unstemmed | An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. |
title_short | An enzyme-linked immunosorbent assay (ELISA) for measurement of heterophile antibody. |
title_sort | enzyme-linked immunosorbent assay (elisa) for measurement of heterophile antibody. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2596542/ https://www.ncbi.nlm.nih.gov/pubmed/6763815 |
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