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Immunodiagnosis of paramphistomosis using monoclonal antibody-based sandwich ELISA for detection of Paramphistomum gracile circulating 16 kDa antigen

机译:使用单克隆抗体的夹心ELISA进行参数致术的免疫诊断检测参数液体涂层循环16kDa抗原

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In this study, we have produced a monoclonal antibody (MoAb) against 16 kDa antigen of Paramphistomum gracile (16 kDaAgPg), and developed an accurate sandwich enzyme-linked immunosorbent assay (sandwich ELISA) for the detection of circulating 16 kDaAg in the serum and fecal samples from cattle naturally infected with P. gracile. MoAb 1D10 was immobilized on a microtitre plate, and the antigen in the samples was captured and detected with biotinylated rabbit anti-16 kDaAgPg antibody. The lower detection limit of sandwich ELISA was 3.5 pg mL(-1), and no cross-reaction with other parasite antigens was evaluated. The reliability of the assay was examined using the serum and fecal samples from cattle naturally infected with P. gracile, Fasciola gigantica, Moniezia benedeni, Trichuris sp., Strongyloides sp., strongylids and non-infected animals. The sandwich ELISA showed the sensitivity, specificity and accuracy at 98.33, 100 and 99.55% (serum samples), and 96.67, 100 and 99.09% (fecal samples). Therefore, this detection method is a rapid and excellent potential assay for the accurate diagnosis of paramphistomosis.
机译:在这项研究中,我们已经产生了单克隆抗体(MoAb),其针对16 kDa副术玻璃综合体(16kdaagpg)的16kDa抗原,并开发了一种精确的夹心酶联免疫吸附试验(夹心ELISA),用于检测血清中的16kdaAg循环16kdaag。来自牛的粪便样本自然感染P.涂层。将MoAb 1d10固定在微量滴定板上,并用生物素化的兔抗16kdaagpg抗体捕获并检测样品中的抗原。夹层ELISA的较低检测极限为3.5pg ml(-1),评价与其他寄生虫抗原的交叉反应。检查测定的可靠性,采用血清和粪便自然感染的牛涂料,粉刺,Fasciola gigantica,Moniezia Benedeni,Trichuris sp.,φ,肌腱和未感染动物的粪便样本。夹心ELISA显示出98.33,100和99.55%(血清样品)和96.67,100和99.09%(粪便样品)的敏感性,特异性和准确性。因此,这种检测方法是一种快速且优异的潜在测定,用于准确诊断参数术。

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