Kong S E, Heel K A, Hall J C, McCauley R D
The University Department of Surgery, Royal Perth Hospital, Perth, Australia.
Mol Cell Probes. 1998 Oct;12(5):339-41. doi: 10.1006/mcpr.1998.0183.
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.
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。