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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Label-free and nicking enzyme-assisted fluorescence signal amplification for RNase H determination based on a G-quadruplexe/thioflavin T complex
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Label-free and nicking enzyme-assisted fluorescence signal amplification for RNase H determination based on a G-quadruplexe/thioflavin T complex

机译:基于G-Quadreplede / Thioflavin T复合物的RNase H测定的无标记和切口酶辅助荧光信号放大

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摘要

In this paper, we describe a novel, label-free and nicking enzyme-assisted fluorescence signal amplification strategy that demonstrates to be cost efficient, sensitive, and unique for assaying the RNase H activity and inhibition based on G-quadruplex formation using a thioflavin T (ThT) dye. This novel assay method is able to detect RNase H with a detection limit of 0.03 U /mL and further exhibits a good linearity R-2 = 0.9923 at a concentration range of 0.03-1 U/mL under optimized conditions. Moreover, the inhibition effect of gentamycin on the RNase H activity is also studied. This strategy provides a potential tool for the biochemical enzyme analysis and inhibitor screening.
机译:在本文中,我们描述了一种新颖的,无标记和切口的酶辅助荧光信号扩增策略,其表明是使用硫蛋白T的基于G-Quadflex形成的RNase H活性和抑制来成本效率,敏感和独特的成本效率,敏感和独特 (tht)染料。 该新型测定方法能够检测RNase H,检测限度为0.03u / ml,并且在优化条件下,在0.03-1u / ml的浓度范围内呈现良好的线性R-2 = 0.9923。 此外,还研究了庆大霉素对RNase H活性的抑制作用。 该策略为生化酶分析和抑制剂筛选提供了一种潜在的工具。

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