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用于定量脊髓灰质炎病毒D抗原的直接酶联免疫吸附测定(ELISA)。

Direct enzyme linked immunosorbent assay (ELISA) for quantification of poliomyelitis virus D-antigen.

作者信息

Souvras M, Montagnon B, Fanget B, van Wezel A L, Hazendonk A G

出版信息

Dev Biol Stand. 1980;46:197-202.

PMID:6244997
Abstract

The proposed micro-ELISA assay by means of the double antibody method involves three steps: adsorption of type specific antiserum on micro-wells; simultaneous incubation of antigen and Horse Radish Peroxydase (HRPO) conjugated antiserum; substrate incubation followed by photometric measurement of absorbance at 403 nm. Preliminary results seem generally in good agreement with those obtained by other tests such as gel diffusion and indirect ELISA.

摘要

所提出的采用双抗体法的微量酶联免疫吸附测定法包括三个步骤

将型特异性抗血清吸附于微孔板上;同时孵育抗原和辣根过氧化物酶(HRPO)偶联抗血清;进行底物孵育,随后在403nm处进行吸光度的光度测量。初步结果似乎总体上与通过其他检测方法(如凝胶扩散和间接酶联免疫吸附测定)所获得的结果高度一致。

引用本文的文献

1
Evaluation of a poliovirus-binding inhibition assay as an alternative to the virus neutralization test.
Clin Diagn Lab Immunol. 1997 Nov;4(6):659-64. doi: 10.1128/cdli.4.6.659-664.1997.
2
Detection of poliovirus antigen by enzyme immunoassay.
J Clin Microbiol. 1987 Sep;25(9):1815-6. doi: 10.1128/jcm.25.9.1815-1816.1987.

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