| 薛慧慧 马骁骁 朱长保 晁天柱 肖君华 周宇荀.改进茎环引物RT-PCR 法实时定量检测microRNA[J].,2014,14(28):5431-5435 |
| 改进茎环引物RT-PCR 法实时定量检测microRNA |
| Real-time Quantification of MicroRNA by ImprovedStem-loop Primer RT-PCR |
| |
| DOI： |
| 中文关键词: miRNA RT-PCR 茎环引物 引物延伸 |
| 英文关键词: miRNA RT-PCR Stem-loop primer Primer extension |
| 基金项目:中央高校基本科研业务费专项资金（13D110521）；国家自然科学基金项目（31171199） |
|
| 摘要点击次数: 744 |
| 全文下载次数: 2450 |
| 中文摘要: |
| 目的：为检测不同组织中microRNA（miRNA）的表达量，本研究建立了一种改进的qRT-PCR（Quantitative reverse transcription
PCR）技术。方法：采用具有高特异性的茎环引物逆转录，结合SYBR Green 实时定量PCR 技术，建立了以延伸茎环引物
RT-PCR 为基础的实时定量检测microRNA 的方法。结果：本研究建立的microRNA 检测方法，特异性好，灵敏度高，线性范围宽。
熔解曲线的单一峰型和电泳检测到的单一条带都证明了扩增的特异性。对标准品的检测跨越了7 个数量级的浓度范围，最低拷
贝数为103，效率高达98%。结论：利用该技术检测了120 个组织样本，说明该方法可快速、准确、高效的获取不同组织中miRNA
的表达量，为进一步探讨miRNA对性发育的影响提供了实验依据。 |
| 英文摘要: |
| Objective:To establish an improved qRT-PCR (Quantitative reverse transcription PCR) technology to detect the
expression levels of microRNA (miRNA) in different tissues.Methods:Reverse transcription using high specific stem-loop primer and
amplified by SYBR Green real-time PCR, established real-time quantitative method of miRNA based on the stem-loop primer extension
RT-PCR.Results:This method was specificity, sensitivity and had a high dynamic range. A single dissociation peak on the thermal
melting curve and a single DNA band on agarose gel signified the amplification reliability and specificity for miRNA. It exhibited a
dynamic range of seven orders of magnitude from 103 to 109, efficiency was up to 98 %.Conclusion:This assay is a fast, accurate and
efficient method to quantification of miRNA indicated by detection of 120 tissue samples, provides an experimental basis for further
investigate the effects of miRNA on sexual development. |
|
查看全文
查看/发表评论 下载PDF阅读器 |
| 关闭 |
