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Rolling circle amplification and circle-to-circle amplification of a specific gene integrated with electrophoretic analysis on a single chip

机译:在单个芯片上整合了电泳分析的特定基因的滚环扩增和环间扩增

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摘要

We have developed an integrated platform for rolling circle amplification (RCA) and circle-to-circle amplification (C2CA) of circular probe (padlock probe) and subsequent microchip electrophoretic detection of a specific gene on a poly(methyl methacrylate) microchip. RCA and C2CA were successfully carried out at a steady temperature of 37 degrees C in the sample well of the microchip, and their respective product was detected on the same channel of the microchip, which was prefilled with a polymer separation matrix and fluorescent dye. Using a species-specific padlock probe for bacterial pathogen V. cholerae, a 25-ng bacterial genomic DNA could be detected in less than 65 min (including RCA and microchip electrophoresis) by this platform. Stable dsDNA C2CA product of genomic DNA for V. cholerae can be detected with the introduced integrated platform. Furthermore, the usefulness of this technique for the monitoring of RCA was demonstrated. This integrated platform provides a sensitive, fast, high-throughput, and reproducible method for signal amplification and detection of the padlock probes in the same microchip and is a promising tool for highly specific gene detection strategies.
机译:我们已经开发了一个集成平台,用于圆形探针(挂锁探针)的滚环扩增(RCA)和环到环扩增(C2CA),以及随后在聚甲基丙烯酸甲酯微芯片上对特定基因进行微芯片电泳检测。 RCA和C2CA已在微芯片样品孔中于37摄氏度的稳定温度下成功进行,并且在微芯片的同一通道中检测到它们各自的产物,该通道已预先填充了聚合物分离基质和荧光染料。使用针对细菌病原体霍乱弧菌的物种特异性挂锁探针,该平台可在不到65分钟的时间内检测到25 ng细菌基因组DNA(包括RCA和微芯片电泳)。霍乱弧菌基因组DNA的稳定dsDNA C2CA产物可以通过引入的整合平台进行检测。此外,证明了该技术对RCA的监测的有用性。该集成平台提供了一种灵敏,快速,高通量且可重现的方法,用于在同一微芯片中进行信号放大和挂锁探针的检测,是用于高度特异性基因检测策略的有前途的工具。

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