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首页> 外文期刊>Analytical Letters >Construction of Three Single-Chain Antibody Fragment Variable Fusion Structures for Sensitive Detection of Nucleocapsid Protein of Hantaan Virus
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Construction of Three Single-Chain Antibody Fragment Variable Fusion Structures for Sensitive Detection of Nucleocapsid Protein of Hantaan Virus

机译:灵敏检测汉坦病毒核衣壳蛋白的三种单链抗体片段可变融合结构的构建

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Three single-chain fragment variable(scFv)fusion structures were constructed for use in rapid and sensitive detection of nucleocapsid protein(NP)of Hantaan virus.The detection of NPs on glass chips was signalized by enzyme labeling or fluorescence dye Cy3,or Cy5 cluster nanoparticles.The sensitivity of the methods with different signal systems was evaluated and compared.The detection limits of scFv-alkaline phosphatase fusion,fluorescence labeling(scFv-Cy3),and nanoparticles labeling(scFv-SBP-streptavidin-nanoparticle)were 0.1 mu g/mL,1 ng/mL,and 0.1 ng/mL NP,respectively,which were all lower than that in a conventional enzyme-linked immunosorbent assay(ELISA)(1 mu g/mL).Twenty Hantaan virus isolates were detected using the proposed methods.
机译:构建了三个单链片段可变(scFv)融合结构,用于快速,灵敏地检测汉坦病毒的核衣壳蛋白(NP)。酶标记或荧光染料Cy3或Cy5簇指示玻璃芯片上NP的检测评价和比较了不同信号系统方法的灵敏度.scFv-碱性磷酸酶融合,荧光标记(scFv-Cy3)和纳米颗粒标记(scFv-SBP-链霉亲和素-纳米颗粒)的检测限为0.1μg / NP,1 ng / mL和0.1 ng / mL NP,分别低于常规酶联免疫吸附试验(ELISA)的1 ng / mL和1 ng / mL。使用该方法检测到20株汉坦病毒分离株。建议的方法。

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