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Selection of suitable reference genes for normalization of genes of interest in canine soft tissue sarcomas using quantitative real-time polymerase chain reaction

机译:使用定量实时聚合酶链反应选择合适的参考基因以对犬软组织肉瘤中的目标基因进行标准化

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摘要

Quantitative real-time reverse transcription polymerase chain reaction (RT-qPCR) is a sensitive technique for quantifying gene expression. Stably expressed reference genes are necessary for normalization of RT-qPCR data. Only a few articles have been published on reference genes in canine tumours. The objective of this study was to demonstrate how to identify suitable reference genes for normalization of genes of interest in canine soft tissue sarcomas using RT-qPCR. Primer pairs for 17 potential reference genes were designed and tested in archival tumour biopsies from six dogs. The geNorm algorithm was used to analyse the most suitable reference genes. Eight potential reference genes were excluded from this final analysis because of their dissociation curves. beta-Glucuronidase (GUSB) and proteasome subunit, beta type, 6 (PSMB6) were most stably expressed with an M value of 0.154 and a CV of 0.053 describing their average stability. We suggest that choice of reference genes should be based on specific testing in every new experimental set-up.
机译:实时定量逆转录聚合酶链反应(RT-qPCR)是量化基因表达的灵敏技术。稳定表达的参考基因对于RT-qPCR数据的标准化必不可少。关于犬肿瘤的参考基因只发表了几篇文章。这项研究的目的是证明如何使用RT-qPCR在犬软组织肉瘤中鉴定合适的参考基因以使目的基因正常化。设计了17种潜在参考基因的引物对,并在六只狗的档案肿瘤活检中进行了测试。 geNorm算法用于分析最合适的参考基因。由于其解离曲线,八个潜在的参考基因被排除在最终分析之外。 β-葡萄糖醛酸苷酶(GUSB)和蛋白酶体亚基,β型6(PSMB6)最稳定地表达,其M值为0.154,CV为0.053,描述了它们的平均稳定性。我们建议参考基因的选择应基于每个新实验设置中的特定测试。

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