基于荧光检测荧光分离技术的液相色谱多重基因表达分析

IF 1.8 Q3 CHEMISTRY, ANALYTICAL
Kenichiro TODOROKI, Chiemi MIYAUCHI, Tatsunosuke TOMITA, Jun Zhe MIN, Koichi INOUE, Toshimasa TOYO'OKA
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引用次数: 0

摘要

我们开发了一种综合分析基因表达水平的方法,将荧光-荧光杂交探针、全氟烷基标记修饰的寡核苷酸和荧光探针与荧光液相色谱(LC) -荧光检测相结合。使用该探针进行Taq聚合酶链反应(PCR)时,根据靶向模板基因的数量释放荧光单核苷酸。由于每个探针的荧光探针的连接体长度和核碱基类型不同,因此LC可以分析多个基因的表达水平,作为荧光单核苷酸的产生量。未进行Taq PCR反应的多余未反应探针在作为预处理柱引入的含氟LC柱中选择性吸附去除。本研究建立的方法允许同时LC定量三个管家基因。此外,建立了同时分析9个基因表达水平的LC分离条件,成功实现了脂多糖刺激白细胞中细胞因子基因的综合检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liquid Chromatography Based Multiplex Gene Expression Analysis Using Fluorous Separation Technique with Fluorescence Detection
We have developed a comprehensive method for analyzing gene expression levels by combining the fluorous-fluorescence hybrid probes, oligonucleic acids modified with a perfluoroalkyl tag and fluorescent probes, with the fluorous liquid chromatography (LC) – fluorescence detection. When Taq polymerase chain reaction (PCR) was performed using this probe, fluorescent mononucleotides were released according to the amount of template gene targeted. Because each probe differs in the linker length of the fluorescent probe and the type of nucleobase, multiple gene expression levels can be analyzed by LC as the amount of fluorescent mononucleotides produced. The excess unreacted probe, which did not undergo the Taq PCR reaction, was selectively removed by adsorption in the fluorous LC column introduced as a pretreatment column. The method established in this study allows simultaneous LC quantification of three housekeeping genes. In addition, LC separation conditions for the simultaneous analysis of nine gene expression levels were established, and comprehensive detection of cytokine genes in lipopolysaccharide-stimulated leukocytes was successfully achieved.
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来源期刊
Chromatography
Chromatography CHEMISTRY, ANALYTICAL-
自引率
64.70%
发文量
19
审稿时长
8 weeks
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