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Rapid Amplification-Free Microarray-Based Ultrasensitive Detection of DNA

机译:基于快速的扩增微阵列的DNA超细瘤检测

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We present a multiplex microarray-based assay of DNA fragments, which allows the detection of less than 10000 DNA fragments in a sample of 100 mu L (corresponding to similar to 0.1 fM analyte concentration) in less than 5 min. High speed and sensitivity are due to three main features of the assay. First, biotinylated adapter oligonucleotides are hybridized to the DNA fragment. Second, it is electrophoretically concentrated from the sample onto the microarray. Third, biotin labels are detected by scanning the microarray surface with streptavidin-coated magnetic beads. Prior to analysis, dsDNA fragments and genomic DNA samples were first denatured and then annealed in the presence of blocking oligonucleotides, generating ssDNA fragments capable of hybridizing with oligonucleotide probes on the microarray. The multiplexity of the assay system was demonstrated by the simultaneous detection of the genomic DNAs of three microorganisms: E. coli, B. cereus, and M. neoaurum.
机译:我们介绍了DNA片段的基于多重微阵列的测定,其允许在少于5分钟的100μL(对应于0.1Fm分析物浓度)的样品中检测小于10000的DNA片段。 高速和敏感性是由于测定的三个主要特征。 首先,生物素化的衔接子寡核苷酸与DNA片段杂交。 其次,将其从样品电泳浓缩到微阵列上。 第三,通过用链霉抗生物素蛋白涂覆的磁珠扫描微阵列表面来检测生物素标记。 在分析之前,首先使DSDNA片段和基因组DNA样品进行变性,然后在阻断寡核苷酸存在下退火,产生能够在微阵列上与寡核苷酸探针杂交的SSDNA片段。 通过同时检测三种微生物的基因组DNA来证明测定系统的复用性:大肠杆菌,B.Cereus和M. Neoaurum。

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