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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Label-free detection of microRNA: two-stage signal enhancement with hairpin assisted cascade isothermal amplification and light-up DNA-silver nanoclusters
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Label-free detection of microRNA: two-stage signal enhancement with hairpin assisted cascade isothermal amplification and light-up DNA-silver nanoclusters

机译:MicroRNA的无标签检测:双阶段信号增强与发夹辅助级联等温扩增和升高DNA-银纳米团簇

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摘要

A method is described for the determination of microRNAs via two-stage signal enhancement. This is attained by combining hairpin (HP) assisted cascade isothermal amplification with light-up DNA-Ag nanoclusters. A rationally designed dual-functional HP is used, and microRNA-21 is chosen as a model analyte. At the first stage, upon the hybridization of the microRNA-21 with HP, microRNA recycling via polymerase-displacement reaction and a circulative nicking-replication process are achieved. This generates numerous G-abundant overhang DNA sequences. In the second stage, the above-released G-abundant overhang DNA sequences hybridize with the dark green Ag NCs, and this results in the appearance of bright red fluorescence. Thanks to the two signal enhancement processes, a linear dependence between the fluorescence intensity at 616 nm and the concentration of microRNA-21 is obtained in the range from 1 pM to 20 pM with a detection limit of 0.7 pM. The strategy clearly discriminates between perfectly-matched and mismatched targets. The method was applied to the determination of microRNA-21 in a spiked serum sample.
机译:描述通过两级信号增强来确定微大RNA的方法。通过将发夹(HP)辅助级联等温扩增与亮度DNA-AG纳米团簇相结合来实现这一点。使用合理设计的双官能HP,并选择MicroRNA-21作为模型分析物。在第一阶段,在MicroRNA-21与HP的杂交后,实现通过聚合酶 - 位移反应再循环和循环切口复制过程的MicroRNA。这产生了众多G丰过突出的DNA序列。在第二阶段,上述释放的G丰突出的DNA序列与深绿Agns杂交,这导致明亮的红色荧光的外观。由于两个信号增强过程,在616nm处的荧光强度与microRNA-21的浓度之间的线性依赖性在1pm至20μm的范围内,检测限为0.7μm。该策略明确区分了完美匹配和不匹配的目标。将该方法应用于尖刺血清样品中MicroRNA-21的测定。

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