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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Detection of microRNA using enzyme-assisted amplifying and DNA-templated silver nanoclusters signal-off fluorescence bioassay
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Detection of microRNA using enzyme-assisted amplifying and DNA-templated silver nanoclusters signal-off fluorescence bioassay

机译:使用酶辅助扩增和DNA模板银纳米蛋白的荧光生物测定法检测MicroRNA

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摘要

A Simple and fast analysis strategy of fluorescence quenching based on DNA-templated silver nanoclusters was developed for detection of miR-122 related to diseases such as human liver. We used Exo III to cleave the silver cluster template and assist in the DNA-RNA complex cycle. When the target is absent, the silver cluster template remains intact, and DNA-AgNCs are generated under the action of AgNO3/NaBH4, producing a strong background fluorescence signal. Once the target is added, the site of the Exo III occurs after a series of hybridization cycles, the Exo III acts, the template DNA is continuously hydrolyzed, and the fluorescence intensity of the system is significantly reduced. By comparing the changes in the fluorescence signal, we found that this strategy has good sensitivity and the detection limit is as low as 84.0 pM. The strategy also has excellent discriminating ability and good selectivity, it can provide a persuasive reference for the early diagnosis of liver cancer and hepatitis.
机译:基于DNA模板银纳米团簇的荧光猝灭荧光猝灭的简单和快速分析策略用于检测与人肝如人肝如人类疾病相关的miR-122。我们使用EXO III将银色群集模板切割并辅助DNA-RNA复合循环。当目标不存在时,银簇模板保持完整,并且DNA-AGNC在AgNO3 / NaBH4的作用下产生,产生强大的背景荧光信号。一旦添加靶,就会在一系列杂交循环后发生EXO III,EXO III作用,模板DNA连续水解,系统的荧光强度显着降低。通过比较荧光信号的变化,我们发现该策略具有良好的敏感性,检测极限低至84.0 pm。该策略还具有良好的辨别能力和良好的选择性,它可以为早期诊断肝癌和肝炎提供有说服力的参考。

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