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Nanoliter high throughput quantitative PCR

机译:纳升高通量定量PCR

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摘要

Understanding biological complexity arising from patterns of gene expression requires accurate and precise measurement of RNA levels across large numbers of genes simultaneously. Real time PCR (RT-PCR) in a microtiter plate is the preferred method forquantitative transcriptional analysis but scaling RT-PCR to higher throughputs in this fluidic format is intrinsically limited by cost and logistic considerations. Hybridization microarrays measure the transcription of many thousands of genes simultaneously yet are limited by low sensitivity, dynamic range, accuracy and sample throughput. The hybrid approach described here combines the superior accuracy, precision and dynamic range of RT-PCR with the parallelism of a microarray in an array of 3072 realtime, 33 nl polymerase chain reactions (RT-PCRs) the size of a microscope slide. RT-PCR is demonstrated with an accuracy and precision equivalent to the same assay in a 384-well microplate but in a 64-fold smaller reaction volume, a 24-fold higher analytical throughput and a workflow compatible with standard microplate protocols.
机译:要了解由基因表达模式引起的生物学复杂性,就需要同时准确,准确地测量大量基因中RNA的水平。微量滴定板中的实时PCR(RT-PCR)是定量转录分析的首选方法,但在这种流体形式下将RT-PCR缩放至更高的通量本质上受到成本和物流考虑的限制。杂交微阵列可同时测量成千上万个基因的转录,但受到低灵敏度,动态范围,准确性和样品通量的限制。本文所述的混合方法将RT-PCR的卓越准确性,精密度和动态范围与微阵列的平行性相结合,可实现显微镜载玻片大小的3072实时,33 nl聚合酶链反应(RT-PCR)阵列。 RT-PCR的准确度和精密度与384孔微孔板中的相同测定法相当,但反应体积小64倍,分析通量高24倍,并且工作流程与标准微孔板规程兼容。

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