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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Development of colloidal gold-based immunochromatographic assay for rapid detection of Mycoplasma suis in porcine plasma
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Development of colloidal gold-based immunochromatographic assay for rapid detection of Mycoplasma suis in porcine plasma

机译:胶体金免疫层析法快速检测猪血浆猪支原体的开发

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摘要

A one-step immunochromatographic assay using gold nanoparticles coated with polyclonal antibody (pAb) against Mycoplasma suis (M. suis) was developed in this study for the detection of M. suis in porcine plasma. The colloidal gold was prepared by the reduction of gold salt with sodium citrate coupled with pAb against M. suis. The pAb was produced by immunizing the BALB/c mice with recombinant MSG1 (rMSG1) protein from M. suis expressed in Escherichia coli. The optimal concentrations of the capture antibody and the coating antibody were 12 μg/ml and 1.5 mg/ml, respectively, and that of the blocking buffer was 1% bovine serum albumin. The lower detection limit of the immunochromatographic assay test was 100 ng/ml with visual detection under optimal conditions of analysis. Classical swine fever virus, porcine reproductive and respiratory syndrome virus, swine pneumonia mycoplasma, swine toxoplasma, and porcine parvovirus were used to evaluate the specificity of the immunochromatographic strips. No cross-reaction of the antibodies with other related swine pathogens was observed. This qualitative test based on the visual evaluation of the results did not require any equipment. The assay time for M. suis detection was less than 10 min, suitable for rapid detection at the grassroots level. The one-step colloidal gold immunochromatographic strips that we developed had high specificity and sensitivity. Therefore, this method would be feasible, convenient, rapid, and effective for detecting M. suis in porcine plasma.
机译:在这项研究中,开发了一种使用金纳米颗粒包被抗猪支原体(猪支原体)的多克隆抗体(pAb)的一步免疫色谱法,用于检测猪血浆中的猪支原体。胶体金是通过用柠檬酸钠和抗猪链球菌的pAb还原金盐来制备的。通过用大肠杆菌中表达的猪M.suis的重组MSG1(rMSG1)蛋白免疫BALB / c小鼠来生产pAb。捕获抗体和包被抗体的最佳浓度分别为12μg/ ml和1.5 mg / ml,封闭缓冲液的最佳浓度为1%牛血清白蛋白。免疫色谱分析测试的下限为100 ng / ml,在最佳分析条件下进行目测。使用经典的猪瘟病毒,猪繁殖与呼吸综合征病毒,猪肺炎支原体,猪弓形虫和猪细小病毒来评估免疫层析条的特异性。没有观察到抗体与其他相关猪病原体的交叉反应。基于结果的视觉评估的定性测试不需要任何设备。猪链球菌检测时间少于10分钟,适合在基层快速检测。我们开发的一步胶体金免疫层析条具有很高的特异性和敏感性。因此,该方法对于检测猪血浆中的猪分枝杆菌是可行,方便,快速,有效的。

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