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Ultrasensitive detection of site-specific DNA methylation by loop-mediated isothermal amplification

机译:通过环介导的等温扩增超灵敏检测位点特异性DNA甲基化

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摘要

A novel loop-mediated isothermal amplification (LAMP)-based methylation assay for simple, robust and cost-effective detection of site-specific DNA methylation has been developed. DNA targets are first treated with methylation-sensitive restriction endonuclease (HpaII), where the DNA targets will be cleaved at specific unmethylated-cytosine residues while leaving the methylated DNA intact. Subsequently, the methylated DNA targets can serve as templates to perform LAMP for the detection of DNA methylation with real-time fluorescence measurements by using a common fluorescent dye (SYBR Green I). Taking advantage of the simplicity and high specificity of HpaII digestion and the isothermal nature and high sensitivity of LAMP, the proposed assay can greatly simplify the detection of DNA methylation and achieve ultrahigh sensitivity and specificity. With this assay, as low as 10 aM methylated DNA can be detected and 0.1% methylated DNA can be determined in the presence of a large excess of unmethylated DNA.
机译:已经开发了一种新颖的基于环介导的等温扩增(LAMP)的甲基化检测方法,用于简单,可靠和经济高效地检测位点特异性DNA甲基化。首先用甲基化敏感的限制性核酸内切酶(HpaII)处理DNA靶标,其中DNA靶标将在特定的未甲基化胞嘧啶残基处裂解,而使甲基化DNA保持完整。随后,甲基化的DNA靶可以用作模板,以执行LAMP,通过使用常见的荧光染料(SYBR Green I)进行具有实时荧光测量的DNA甲基化检测。利用HpaII消化的简单性和高特异性以及LAMP的等温性质和高灵敏度,所提出的测定方法可以大大简化DNA甲基化的检测,并实现超高灵敏度和特异性。通过这种测定,可以检测到低至10 aM的甲基化DNA,并且在存在大量过量的未甲基化DNA的情况下可以测定0.1%的甲基化DNA。

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