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首页> 外文期刊>Journal of nanoscience and nanotechnology >A Nanoscale Mutation-Sensitive On/Off Switch Based Assays for the Detection of Hepatitis B Virus Lamivudine-Resistant Mutations
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A Nanoscale Mutation-Sensitive On/Off Switch Based Assays for the Detection of Hepatitis B Virus Lamivudine-Resistant Mutations

机译:基于纳米突变敏感的开/关开关的检测乙型肝炎病毒拉米夫定耐药突变的方法。

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Long-term usage of lamivudine in the treatment of chronic hepatitis B virus (HBV) infection induces the emergence of drug resistance. Sensitive and specific methods aimed at detecting the mutants are clinically useful and required. The purpose of this study was to develop methods for detecting the mutations of YMDD, rtL180M, and rtV173L by nanoscale mutation-sensitive switch consisting of high fidelity polymerase and phosphorothioate-modified allele specific primers. Four assays for these hotspot mutations have been developed with the sensitivity of 100 copies and specificity of at least three log scales for matched templates over mismatched templates. In the condition of multiplex PCR, the sensitivities of these assays are approximately 1000 copies and specificities with two log scales in discrimination of mutant alleles over wild type sequences. These newly developed assays are rapid, accurate, and cost-efficient in detection of lamivudine-related HBV mutants.
机译:长期使用拉米夫定治疗慢性乙型肝炎病毒(HBV)感染会引起耐药性的出现。旨在检测突变体的灵敏且特异的方法在临床上是有用且必需的。这项研究的目的是开发通过纳米级突变敏感开关检测YMDD,rtL180M和rtV173L突变的方法,该开关由高保真聚合酶和硫代磷酸酯修饰的等位基因特异性引物组成。已经开发了针对这些热点突变的四种检测方法,其灵敏度为100份拷贝,而匹配模板比错配模板的特异性至少为3个对数刻度。在多重PCR的条件下,这些测定的灵敏度约为1000个拷贝,并且在区分野生型序列的突变等位基因时具有两个对数刻度的特异性。这些新开发的检测方法可快速,准确且经济高效地检测拉米夫定相关的HBV突变体。

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