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Impact of Reference Gene Selection for Target Gene Normalization on Experimental Outcome Using Real-Time qRT-PCR in Adipocytes

机译:使用实时qRT-PCR在脂肪细胞中参考基因选择对靶基因正常化的影响对实验结果的影响

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摘要

BackgroundWith the current rise in obesity-related morbidities, real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) has become a widely used method for assessment of genes expressed and regulated by adipocytes. In order to measure accurate changes in relative gene expression and monitor intersample variability, normalization to endogenous control genes that do not change in relative expression is commonly used with qRT-PCR determinations. However, historical evidence has clearly demonstrated that the expression profiles of traditional control genes (e.g., β-actin, GAPDH, α-tubulin) are differentially regulated across multiple tissue types and experimental conditions.
机译:背景技术随着当前与肥胖相关的发病率的上升,实时定量逆转录聚合酶链反应(qRT-PCR)已成为评估脂肪细胞表达和调控基因的一种广泛使用的方法。为了测量相对基因表达的准确变化并监测样品间的变异性,通常将定量表达相对不变的内源对照基因进行标准化,用于qRT-PCR测定。但是,历史证据清楚地表明,传统的对照基因(例如,β-肌动蛋白,GAPDH,α-微管蛋白)的表达谱在多种组织类型和实验条件下受到差异调节。

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