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借助斑点酶联免疫吸附测定法(Dot-ELISA)筛查破伤风抗体。使用标准酶联免疫吸附测定法(ELISA)和被动血凝试验验证结果。

Screening of tetanus antibodies with the aid of dot-enzyme-linked immunosorbent assay (Dot-ELISA). Validation of the results using standard ELISA and passive hemagglutination test.

作者信息

Bizzini B, Leonardi M S, Zummo S, Mastroeni P

机构信息

Microbiology Institute, University of Messina, Italy.

出版信息

Boll Ist Sieroter Milan. 1990 Jun;69(2):391-3.

PMID:2152298
Abstract

A Dot-ELISA is described that lends itself to the screening of large series of sera in relation to tetanus antibodies. A threshold of 0.06 I.U. per ml has been chosen as representing the protective tetanus antibody level. Two hundred and fifty-four sera were assayed by conventional ELISA, passive hemagglutination test and Dot-ELISA. The results obtained using concurrently these 3 techniques were in agreement with one another and permitted us to ascribe the same sera as tested by the various techniques to the same group of sera containing a non protective antitetanus antibody level and to the same group of sera-containing a protective level. It is suggested that Dot-ELISA should be used for the assessment of the tetanus immune status of populations.

摘要

本文描述了一种斑点酶联免疫吸附测定法(Dot-ELISA),该方法适用于针对破伤风抗体对大量血清进行筛查。已选择每毫升0.06国际单位的阈值作为代表保护性破伤风抗体水平。采用传统酶联免疫吸附测定法、被动血凝试验和斑点酶联免疫吸附测定法对254份血清进行了检测。同时使用这三种技术获得的结果相互一致,使我们能够将通过各种技术检测的相同血清归为含有非保护性抗破伤风抗体水平的同一组血清以及含有保护性水平的同一组血清。建议使用斑点酶联免疫吸附测定法评估人群的破伤风免疫状态。

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