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microRNA定量检测方法研究现状 被引量:5

Current research in methods for the quantitative detection of microRNA
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摘要 MicroRNA(miRNA)是一类由18-24 nt核酸构成的非编码内源性小分子RNA,主要参与真核生物的细胞分化、增殖与凋亡等转录后水平的基因表达调控。研究发现,miRNA与肿瘤、代谢调控、疾病发生及诊断等方面有密切的联系,因此准确且灵敏地进行miRNA的定量检测是深入研究miRNA功能的前提。目前,miRNA定量检测原理主要基于核酸杂交或扩增,包括Northern印迹、微阵列芯片、实时定量PCR、滚环扩增等。本文通过对传统miRNA检测方法、高灵敏度新型miRNA检测方法进行阐述与分析,为筛选合适的miRNA定量检测方法提供参考。 MicroRNA( miRNA) is a kind of non-coding endogenous small molecule RNA, which is composed of 18- 24 nt nucleic acid. It is mainly involved in the regulation of cell differentiation,proliferation and apoptosis. Mature miRNA sequence is short, highly conservative, stability and other characteristics, which increases a lot of difficulties for accurate detection of miRNA levels. miRNA quantitative detection principle is mainly based on nucleic acid hybridization or amplification, including Northern bloting,microarray chip, real-time quantitative PCR, rolling ring amplification, etc. Through the analysis of the advantages and disadvantages of the existing miRNA detection technology in recent years,this paper will provide a reference for screening suitable miRNA quantitative detection method.
作者 陈艳琳 王颖芳 CHEN Yanlin WANG Yingfang(School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China)
出处 《广东药学院学报》 CAS 2016年第5期666-670,F0003,共6页 Academic Journal of Guangdong College of Pharmacy
基金 国家自然科学基金青年基金项目(81403195) 广东省自然科学基金项目(S2013010015418)
关键词 MICRORNA 实时定量PCR 滚环扩增 NORTHERN印迹 microRNA quantitative PCR rolling ring amplification Northern bloting
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