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Preparation of a Monoclonal Antibody Based Sandwich Enzyme-Linked Immunosorbent Assay for Salmonella

机译:沙门氏菌单克隆抗体夹心酶联免疫吸附法的制备

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A double antibody sandwich enzyme-linked immunosorbent assay (ELISA) was developed using monoclonal antibodies (mAbs) as a rapid, economical alternative to culture isolation procedures for detection of Salmonella. Through cell fusion technology, five mAbs were screened out, in which A2C6D3 as capture antibody and E3C5E8 as detection antibody were selected for the development of ELISA method. This assay detected all Salmonella serovars, which included representative serovars of serogroups B, C, D, and E and gave negative results for all nonSalmonella species tested. The ELISA had a specificity and sensitivity of 100% and 91%, respectively, and a kappa value of 0.93 relative to the culture methods. Such a sandwich ELISA has the potential to be used in the implementation of the pathogen reduction and hazard analysis critical control point systems as well as in clinical laboratories.
机译:使用单克隆抗体(mAb)开发了一种双抗体夹心酶联免疫吸附测定(ELISA),作为检测沙门氏菌的培养分离程序的一种快速,经济的选择。通过细胞融合技术筛选出5个单克隆抗体,选择A2C6D3作为捕获抗体,选择E3C5E8作为检测抗体,用于ELISA方法的开发。该测定法检测了所有沙门氏菌血清型,其中包括血清型B,C,D和E的代表性血清型,并且对所有非沙门氏菌属菌种均给出了阴性结果。相对于培养方法,ELISA的特异性和敏感性分别为100%和91%,kappa值为0.93。这种夹心ELISA有潜力用于实施病原体减少和危害分析关键控制点系统以及临床实验室。

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