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首页> 外文期刊>Journal of nanoscience and nanotechnology >Fluorescent Quantification of DNA Based on Core-Shell Fe3O4@SiO2@Au Nanocomposites and Multiplex Ligation-Dependent Probe Amplification
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Fluorescent Quantification of DNA Based on Core-Shell Fe3O4@SiO2@Au Nanocomposites and Multiplex Ligation-Dependent Probe Amplification

机译:基于核-壳Fe3O4 @ SiO2 @ Au纳米复合材料和多重连接依赖性探针扩增的DNA荧光定量。

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摘要

In this research, a novel method for relative fluorescent quantification of DNA based on Fe3O4@SiO2@Au gold-coated magnetic nanocomposites (GMNPs) and multiplex ligation-dependent probe amplification (MLPA) has been developed. With the help of self-assembly, seed-mediated growth and chemical reduction method, core-shell Fe3O4@SiO2@Au GMNPs were synthesized. Through modified streptavidin on the GMNPs surface, we obtained a bead chip which can capture the biotinylated probes. Then we designed MLPA probes which were tagged with biotin or Cy3 and target DNA on the basis of human APP gene sequence. The products from the thermostable DNA ligase induced ligation reactions and PCR amplifications were incubated with SA-GMNPs. After washing, magnetic separation, spotting, the fluorescent scanning results showed our method can be used for the relative quantitative analysis of the target DNA in the concentration range of 0.004 similar to 0.5 mu M.
机译:在这项研究中,已开发出一种基于Fe3O4 @ SiO2 @ Au包金的磁性纳米复合材料(GMNPs)和多重连接依赖探针扩增(MLPA)的DNA相对荧光定量新方法。借助自组装,种子介导的生长和化学还原的方法,合成了核壳型Fe3O4 @ SiO2 @ Au GMNPs。通过在GMNPs表面修饰链霉亲和素,我们获得了可以捕获生物素化探针的微珠芯片。然后根据人APP基因序列设计了标记有生物素或Cy3和目标DNA的MLPA探针。将热稳定的DNA连接酶诱导的连接反应和PCR扩增产物与SA-GMNP一起孵育。清洗,磁分离,点样后,荧光扫描结果表明,本方法可用于浓度范围为0.004的目标DNA的相对定量分析,类似于0.5μM。

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