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METHOD FOR DETERMINING DELETIONS IN HBV PRE-S2 REGION

机译:乙型肝炎病毒前S2区检出病情的方法

摘要

A method of detecting pre-S2 deletion mutant LHBS is 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:本文公开了一种检测前S 2 缺失突变体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;并通过从LHBS蛋白中减去WT LHBS蛋白的量来计算pre-S 2 缺失突变体LHBS蛋白的量。有利地,通过本文所述的方法,前S 2 缺失突变体LHBS的量是肝切除手术后慢性HBV携带者的HCC发生和HCC患者复发的潜在高风险标志。 WT和pre-S突变体LHBS之间没有相互影响的情况下,可以轻松计算出生物学样品,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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