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ANTIBODIES AND METHOD FOR DETERMINING DELETIONS IN HBV PRE-S2 REGION

机译:用于确定HBV pre-S2地区中病情的抗体和方法

摘要

A HBS-specific antibody, a LHBS-specific antibody, a WT LHBS-specific antibody, an immunoassay kit comprising the antibodies, and a method of detecting pre-S2 deletion mutant LHBS using the immunoassay kit are disclosed herein. The method comprises incubating a biological sample with a first antibody to captured HBS proteins; detecting the LHBS and WT LHBS bound to the immobilized first antibody, respectively; and calculating the amount of the pre-S2 deletion mutant LHBS protein by subtracting the amount of the WT LHBS protein from that of the LHBS protein. Advantageously, by the method described herein, the amount of the pre-S2 deletion mutant LHBS, a potential high-risk marker for HCC incidence in chronic HBV carriers and recurrence in HCC patients after hepatectomy surgery, in a biological sample may be easily calculated without mutual influence between the WT and pre-S mutant LHBS while reducing the labor-intensive process for cloning each gene product before analysis.
机译:本文公开了HBS特异性抗体,LHBS特异性抗体,WT LHBS特异性抗体,包含所述抗体的免疫测定试剂盒以及使用该免疫测定试剂盒检测S2缺失前突变体LHBS的方法。该方法包括将生物样品与捕获的HBS蛋白的第一抗体一起孵育;检测分别与固定的第一抗体结合的LHBS和WT LHBS;通过从LHBS蛋白的量中减去WT LHBS蛋白的量,计算S2缺失前突变型LHBS蛋白的量。有利地,通过本文所述的方法,可以容易地计算生物样品中的S2缺失突变体LHBS的量,生物学样品中慢性HBV携带者的HCC发病率和肝癌手术后HCC患者复发的潜在高风险标志物的量。 WT和pre-S突变体LHBS之间的相互影响,同时减少了在分析之前克隆每个基因产物的劳动密集型过程。

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