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Carbodiimide-mediated cross-linking of RNA to nylon membranes improves the detection of siRNA, miRNA and piRNA by northern blot

机译:碳二亚胺介导的RNA与尼龙膜的交联可通过Northern blot改善siRNA,miRNA和piRNA的检测

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摘要

The northern blot, or RNA gel blot, is a widely used method for the discovery, validation and expression analysis of small regulatory RNA such as small interfering RNA (siRNA), microRNA (miRNA) and piwi-interacting RNA (piRNA). Although it is straightforward and quantitative, the main disadvantage of a northern blot is that it detects such RNA less sensitively than most other approaches. We found that the standard dose of UV used in northern blots was not the most efficient at immobilizing small RNA of 20-40 nt on nylon membranes. However, increasing the dose of UV reduced the detection of miRNA by hybridization in northern blotting experiments. We discovered that using the soluble carbodiimide, EDC, to cross-link RNA to nylon membranes greatly improved the detection of small RNA by hybridization. Compared to standard UV cross-linking procedures, EDC cross-linking provided a 25-50-fold increase in the sensitivity of detection of siRNA from plants and miRNA or piRNA from mammalian cells. All types of hybridization probes tested benefited from the new cross-linking procedure. Cross-linking was dependent on a terminal phosphate and so, should be applicable to other related categories of small RNA.
机译:Northern印迹或RNA凝胶印迹是发现,验证和表达分析小调节RNA(例如小干扰RNA(siRNA),microRNA(miRNA)和piwi-interacting RNA(piRNA))的一种广泛使用的方法。尽管它是直接且定量的,但Northern印迹法的主要缺点是与大多数其他方法相比,它检测这类RNA的灵敏度较低。我们发现用于Northern blots的标准UV剂量对于将20-40 nt的小RNA固定在尼龙膜上并不是最有效的。但是,增加UV剂量会减少Northern杂交实验中杂交产生的miRNA检测量。我们发现,使用可溶性碳二亚胺(EDC)将RNA交联到尼龙膜上,可以大大改善杂交检测中小RNA的检测。与标准的UV交联程序相比,EDC交联使植物中siRNA和哺乳动物细胞中miRNA或piRNA的检测灵敏度提高了25-50倍。测试的所有类型的杂交探针均受益于新的交联程序。交联取决于末端磷酸酯,因此,应适用于其他相关类别的小RNA。

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