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通过酶联免疫吸附测定法测定针对脑膜炎球菌抗原的抗体反应。

Determination of antibody responses to meningococcal antigens by ELISA.

作者信息

Rosenqvist E, Käyhty H, Pollard A J

机构信息

Department of Vaccinology, National Institute of Public Health, Oslo, Norway.

出版信息

Methods Mol Med. 2001;66:255-73. doi: 10.1385/1-59259-148-5:255.

Abstract

Enzyme-linked immunosorbent assay (ELISA, EIA) is a highly versatile and sensitive technique that can be used for quantitative as well as qualitative determination of almost any antigen or antibody. Reagents are stable, non-radioactive and, in most cases, commercially available. Owing to the simplicity and versatility of the method, ELISA represents probably one of the most used methods for studying antibody responses and antibody levels. Since Engvall and Perlman's first paper describing the ELISA in 1971 (1), almost all laboratories working in serology or immunology have designed their own assays with different protocols for coating with antigens, incubation conditions, detecting systems, and ways of reporting of the results. In most cases, there is no need for strict interlaboratory standardization of ELISAs and each laboratory will develop a system that suits their needs. However, for some ELISAs, e.g., used in diagnostic laboratories and in vaccine trials, standardization is important, and this is considered in "Meningococcal Disease" Edited by AJ Pollard and MCJ Maiden, (1a).

摘要

酶联免疫吸附测定(ELISA,EIA)是一种高度通用且灵敏的技术,可用于几乎任何抗原或抗体的定量和定性测定。试剂稳定、无放射性,且在大多数情况下可从市场购得。由于该方法的简便性和通用性,ELISA可能是研究抗体反应和抗体水平最常用的方法之一。自1971年Engvall和Perlman首次发表描述ELISA的论文(1)以来,几乎所有从事血清学或免疫学研究的实验室都设计了自己的检测方法,在抗原包被、孵育条件、检测系统以及结果报告方式等方面采用了不同的方案。在大多数情况下,ELISA无需严格的实验室间标准化,每个实验室都会开发适合自身需求的系统。然而,对于某些ELISA,例如用于诊断实验室和疫苗试验的ELISA,标准化很重要,这一点在AJ Pollard和MCJ Maiden编辑的《脑膜炎球菌病》(1a)中有论述。

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