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一种用于检测口蹄疫病毒抗体的新型酶联免疫吸附测定法(ELISA)。I. ELISA的开发与方法。

A new enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies against foot-and-mouth disease virus. I. Development and method of ELISA.

作者信息

Hamblin C, Barnett I T, Hedger R S

出版信息

J Immunol Methods. 1986 Oct 23;93(1):115-21. doi: 10.1016/0022-1759(86)90441-2.

Abstract

A liquid-phase blocking sandwich ELISA has been developed for the quantification of antibodies against foot-and-mouth disease virus which may replace the virus neutralisation (VN) test. This test employs the incubation of a constant amount of antigen with a range of test serum dilutions in the liquid-phase before being assayed using a trapping ELISA. Thus it does not rely on the availability or growth of tissue culture cells. The assay is rapid and relatively simple to perform, reagents are used economically and results may be recorded within 24 h. The ELISA is sensitive and results are more specific and more reproducible than those obtained by VN. Results are expressed as reciprocal antibody titres which are analogous and of a similar order to those recorded by VN. Individual titres, therefore, may be easily assessed by workers in the field who are already familiar with VN.

摘要

已开发出一种用于定量检测口蹄疫病毒抗体的液相阻断夹心酶联免疫吸附测定法(ELISA),该方法可替代病毒中和(VN)试验。此试验采用在液相中将恒定数量的抗原与一系列待测血清稀释液孵育,然后使用捕获ELISA进行检测。因此,它不依赖于组织培养细胞的可用性或生长情况。该测定法快速且操作相对简单,试剂使用经济,结果可在24小时内记录。ELISA灵敏,其结果比VN试验更特异、更具重复性。结果以抗体滴度的倒数表示,与VN试验记录的结果相似且处于相似水平。因此,熟悉VN试验的现场工作人员可轻松评估个体滴度。

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