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使用短链聚丙烯酰胺作为筛分介质,通过激光诱导荧光检测的毛细管电泳分析单链构象多态性。

Analysis of single-strand conformation polymorphism by capillary electrophoresis with laser-induced fluorescence detection using short-chain polyacrylamide as sieving medium.

作者信息

Ren J, Ulvik A, Ueland P M, Refsum H

机构信息

Department of Clinical Biology, University of Bergen, Norway.

出版信息

Anal Biochem. 1997 Feb 1;245(1):79-84. doi: 10.1006/abio.1996.9937.

Abstract

A rapid analysis of single-strand conformation polymorphism (SSCP) by capillary electrophoresis with laser-induced fluorescence (CE-LIF) detector was developed using a short-chain, linear polyacrylamide (PA) as sieving medium. Capillary filling of this low-viscosity medium and medium replacement were carried out by commercial capillary electrophoresis instruments. The approach was successfully applied to detect the C677T mutation of methylenetetrahydrofolate reductase gene. The influences of factors such as the concentration of polymers, voltage, temperature, and additives on the SSCP analysis were systematically investigated. Using 6% PA sieving medium and high electric field, four strands were resolved within 11 min in a DNA sample heterozygous for the C677T mutation, and a characteristic pattern was apparent for each of the three genotypes. When using multiple injection mode, the average analysis time per sample was reduced to about 4 min. In conclusion, our results indicate that CE-LIF may be an alternative to conventional SSCP analysis based on slab gel electrophoresis for the detection of genetic mutations. The technique is simple and rapid and is well suited to analysis of large numbers of clinical samples.

摘要

采用短链线性聚丙烯酰胺(PA)作为筛分介质,开发了一种利用激光诱导荧光(CE-LIF)检测器通过毛细管电泳快速分析单链构象多态性(SSCP)的方法。使用商用毛细管电泳仪器进行这种低粘度介质的毛细管填充和介质更换。该方法成功应用于检测亚甲基四氢叶酸还原酶基因的C677T突变。系统研究了聚合物浓度、电压、温度和添加剂等因素对SSCP分析的影响。使用6% PA筛分介质和高电场,在C677T突变杂合的DNA样品中,11分钟内可分辨出四条链,三种基因型各自呈现出特征性图谱。采用多次进样模式时,每个样品的平均分析时间缩短至约4分钟。总之,我们的结果表明,对于基因突变检测,CE-LIF可能是基于平板凝胶电泳的传统SSCP分析的一种替代方法。该技术简单快速,非常适合大量临床样品的分析。

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