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Signal amplification by rolling circle amplification on DNA microarrays

机译:在DNA微阵列上通过滚环扩增进行信号放大

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摘要

While microarrays hold considerable promise in large-scale biology on account of their massively parallel analytical nature, there is a need for compatible signal amplification procedures to increase sensitivity without loss of multiplexing. Rolling circle amplification (RCA) is a molecular amplification method with the unique property of product localization. This report describes the application of RCA signal amplification for multiplexed, direct detection and quantitation of nucleic acid targets on planar glass and gel-coated microarrays. As few as 150 molecules bound to the surface of microarrays can be detected using RCA. Because of the linear kinetics of RCA, nucleic acid target molecules may be measured with a dynamic range of four orders of magnitude. Consequently, RCA is a promising technology for the direct measurement of nucleic acids on microarrays without the need for a potentially biasing preamplification step.
机译:尽管微阵列由于其大规模平行的分析性质而在大规模生物学中具有可观的前景,但仍需要兼容的信号放大程序以增加灵敏度而又不损失多路复用。滚环扩增(RCA)是一种具有产物定位独特性质的分子扩增方法。该报告描述了RCA信号放大在平板玻璃和凝胶涂层微阵列上对核酸靶标进行多重,直接检测和定量分析中的应用。使用RCA可以检测到多达150个与微阵列表面结合的分子。由于RCA的线性动力学,可以在四个数量级的动态范围内测量核酸靶分子。因此,RCA是一种有前途的技术,可直接测量微阵列上的核酸,而无需潜在的预扩增步骤。

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