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首页> 外文期刊>Journal of Veterinary Science >Development and evaluation of an immunochromatographic assay using a gp51 monoclonal antibody for the detection of antibodies against the bovine leukemia virus
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Development and evaluation of an immunochromatographic assay using a gp51 monoclonal antibody for the detection of antibodies against the bovine leukemia virus

机译:开发和评估使用gp51单克隆抗体的免疫色谱法检测牛白血病病毒的抗体

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Infection of cattle with bovine leukemia virus (BLV) has been observed and reported worldwide, including in Korea. The onsite identification of infected cattle would help decreasing and eradicating BLV infections on farms. Here, we present a new immunochromatographic assay that employs monoclonal antibodies (MAbs) for the detection of antibodies against BLV in the field. BLV envelope glycoprotein (gp)51 was expressed in E. coli, and MAbs against recombinant BLV gp51 were generated for the development of an immunochromatographic assay to detect BLV antibodies in cattle. The sensitivity and specificity of the assay were determined by comparing these results with those obtained from a standard enzyme linked immunosorbent assay (ELISA). A total of 160 bovine sera were used to evaluate the new immunochromatographic assay. Using ELISA as a reference standard, the relative specificity and sensitivity of this assay were determined to be 94.7% and 98%, respectively. Because of its high sensitivity and specificity, this BLV antibody detection assay would be suitable for the onsite identification of BLV infection in the field.
机译:在世界范围内,包括在韩国,都已经观察到牛感染牛白血病病毒(BLV)的报道。对感染牛的现场鉴定将有助于减少和消除农场的BLV感染。在这里,我们提出了一种新的免疫色谱分析方法,该方法采用单克隆抗体(MAb)来检测针对BLV的抗体。 BLV包膜糖蛋白(gp)51在大肠杆菌中表达,并产生了针对重组BLV gp51的单克隆抗体,用于开发免疫色谱法以检测牛的BLV抗体。通过将这些结果与从标准酶联免疫吸附测定(ELISA)获得的结果进行比较,可以确定测定的灵敏度和特异性。总共使用了160个牛血清来评估新的免疫色谱分析。使用ELISA作为参考标准,测定的相对特异性和灵敏度分别为94.7%和98%。由于其高灵敏度和特异性,该BLV抗体检测方法将适合现场鉴定BLV感染。

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