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通过miRFLP分析法对人房水中的微小RNA进行定量分析。

Quantification of MicroRNAs in human aqueous humor by miRFLP assay.

作者信息

Zhu Bijun, Zhu Wenli, Ye Shangyu, Luo Delun, Xu Kai, Wu Zhigang, Zou Haidong

机构信息

Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiaotong University, Shanghai, China.

Chengdu Nuoen Biotechnologies, LTD, Chengdu, China.

出版信息

Exp Eye Res. 2017 Sep;162:73-78. doi: 10.1016/j.exer.2017.07.007. Epub 2017 Jul 15.

Abstract

MiRNAs are expressed in a tissue-specific fashion in the eyes and changes in miRNAs levels in aqueous humor (AH) may reflect the function of the eye and eye disease. Due to the low concentration of total miRNA in human aqueous humor, high volume of sample is required for RNA extraction prior to routine quantification such as RT-qPCR. However, limited volume of AH could be collected through surgery because of the characteristic of the eye. In addition, inefficiency of RNA-extraction kits could affect target miRNA quantification dramatically. AH-direct miRFLP assay was developed for quantification of target miRNAs in human aqueous humor samples. For the first time, accurate miRNA quantification in human AH was achieved with microliter scale sample loading. Higher copy numbers of target miRNAs were obtained in direct detection than in RNA-extraction solution. It indicates that AH-direct miRFLP assay was able to quantify target miRNAs more accurately with no requirement for RNA-extraction to avoid sampling variability.

摘要

微小RNA(miRNAs)以组织特异性方式在眼睛中表达,房水(AH)中miRNAs水平的变化可能反映眼睛的功能和眼部疾病。由于人房水中总miRNA浓度较低,在进行常规定量分析(如逆转录-定量聚合酶链反应,RT-qPCR)之前,需要大量样本进行RNA提取。然而,由于眼睛的特性,通过手术能够收集的房水体积有限。此外,RNA提取试剂盒的效率低下可能会显著影响目标miRNA的定量。开发了房水直接miRFLP分析方法用于定量人房水样本中的目标miRNAs。首次通过微升规模的样本上样实现了人房水中miRNA的准确定量。与RNA提取溶液相比,直接检测获得了更高拷贝数的目标miRNAs。这表明房水直接miRFLP分析方法能够更准确地定量目标miRNAs,无需进行RNA提取以避免采样变异性。

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