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定量竞争性聚合酶链反应:通过激光诱导荧光检测的毛细管电泳分析HIV-1 gag基因的扩增产物。

Quantitative competitive polymerase chain reaction: analysis of amplified products of the HIV-1 gag gene by capillary electrophoresis with laser-induced fluorescence detection.

作者信息

Williams S J, Schwer C, Krishnarao A S, Heid C, Karger B L, Williams P M

机构信息

Department of Analytical Chemistry, Genentech, Inc., 460 Point San Bruno Boulevard, South San Francisco, California, 94080, USA.

出版信息

Anal Biochem. 1996 Apr 5;236(1):146-52. doi: 10.1006/abio.1996.0143.

Abstract

A quantitative competitive polymerase chain reaction (PCR) assay for the detection and quantification of HIV-1 has been developed using capillary electrophoresis. Separation of the PCR products is carried out in coated capillaries filled with replaceable linear polyacrylamide, and detection is performed using laser-induced fluorescence. The quantitative capabilities of this assay are described. We show results from analysis of a noninfectious plasmid encoding the HIV genome and integrated proviral DNA. Potential applications of this assay are discussed.

摘要

已开发出一种使用毛细管电泳检测和定量HIV-1的定量竞争性聚合酶链反应(PCR)检测方法。PCR产物在填充有可替换线性聚丙烯酰胺的涂层毛细管中进行分离,并使用激光诱导荧光进行检测。描述了该检测方法的定量能力。我们展示了对编码HIV基因组的非感染性质粒和整合的前病毒DNA分析的结果。讨论了该检测方法的潜在应用。

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