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使用竞争性逆转录聚合酶链反应对肠细胞中的谷氨酰胺酶信使核糖核酸进行定量分析。

Quantitation of glutaminase mRNA in enterocytes using competitive RT-PCR.

作者信息

Kong S E, Heel K A, Hall J C, McCauley R D

机构信息

The University Department of Surgery, Royal Perth Hospital, Perth, Australia.

出版信息

Mol Cell Probes. 1998 Oct;12(5):339-41. doi: 10.1006/mcpr.1998.0183.

Abstract

The concentration of mRNA within the intestinal mucosa is usually measured by either Northern blot analysis or semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). However, these methods are limited by a lack of valid internal controls, low sensitivity, and large differences in the concentration of the internal control and target gene. The authors present an alternative method using competitive RT-PCR to measure glutaminase mRNA in isolated enterocytes.

摘要

通常通过Northern印迹分析或半定量逆转录聚合酶链反应(RT-PCR)来测量肠黏膜内mRNA的浓度。然而,这些方法存在局限性,缺乏有效的内对照、灵敏度低,且内对照与靶基因的浓度差异较大。作者提出了一种使用竞争性RT-PCR来测量分离的肠上皮细胞中谷氨酰胺酶mRNA的替代方法。

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