首页> 外文会议>International Conference on Miniaturized Systems for Chemistry and Life Sciences >SINGLE QUANTUM DOT-BASED MULTIPLEXED POINT MUTATION DETECTION BY GAP LIGASE CHAIN REACTION
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SINGLE QUANTUM DOT-BASED MULTIPLEXED POINT MUTATION DETECTION BY GAP LIGASE CHAIN REACTION

机译:间隙连接酶链反应的单量子点基复用点突变检测

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We propose an assay which, combines the specificity of gap-filling ligation chain reaction (Gap-LCR) and the sensitivity of quantum dot-single molecule spectroscopy (QD-SMS) to detect point mutation from genomic DNA without pre-PCR amplification. Mutation variant-specific ligation products are generated by Gap-LCR and captured by quantum dot to form DNA-QD nanocomplexes that are detected by SMS. SMS enables measurement of fluorescent bursts emitted from individual molecules, eliminating the need of separation of ligation products. The proposed assay is capable of detecting zeptomoles of KRAS codon 12 mutation variants and allows for detection of multiple types of mutation variants from a single experiment.
机译:我们提出了一种测定,将间隙填充结扎链反应(GAP-LCR)的特异性与量子点单分子光谱(QD-SMS)的敏感性结合在没有预先PCR扩增的情况下从基因组DNA检测点突变。突变变体特异性连接产物由间隙-LCR产生并由量子点捕获以形成通过SMS检测的DNA-QD纳米单链。 SMS能够测量从个体分子发出的荧光突发,消除了连接产物的分离的需要。所提出的测定能够检测KRAC密码子12突变变体的Zeptomols,并允许从单一实验中检测多种类型的突变变体。

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