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An antibody chimera technique applied to enzyme immunoassay for human alpha-1-fetoprotein with monoclonal and polyclonal antibodies.

作者信息

Porstmann B, Avrameas S, Ternynck T, Porstmann T, Micheel B, Guesdon J L

出版信息

J Immunol Methods. 1984 Jan 20;66(1):179-85. doi: 10.1016/0022-1759(84)90260-6.

DOI:10.1016/0022-1759(84)90260-6
PMID:6198399
Abstract

A 2-step enzyme immunoassay (EIA) for human alpha-1-fetoprotein (AFP) is proposed, which uses covalently coupled anti-AFP IgG and anti-horseradish peroxidase (HRP) IgG (antibody chimera) binding HRP as the marker enzyme immunologically. The use of polyclonal and monoclonal anti-AFP linked to anti-HRP antibodies was compared with a conventional 2-site binding EIA with HRP covalently bound to anti-AFP IgG. The sensitivity of the conventional EIA is increased by the use of an antibody chimera comprising a molar ratio of anti-AFP IgG: anti-HRP IgG of 1:8, especially if monoclonal antibodies are employed. This improved sensitivity may be achieved by a very simple coupling procedure without purification of conjugate and with very crude HRP preparations.

摘要

相似文献

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引用本文的文献

1
Progress in enzyme immunoassays: production of reagents, experimental design, and interpretation.酶免疫测定的进展:试剂生产、实验设计及结果解读
Bull World Health Organ. 1985;63(4):793-811.