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Identification of Reference Genes for Normalizing Quantitative Real-Time PCR in Urechis unicinctus
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作者 BAI Yajiao ZHOU Di +4 位作者 WEI Maokai XIE Yueyang GAO Beibei QIN Zhenkui ZHANG Zhifeng 《Journal of Ocean University of China》 SCIE CAS CSCD 2018年第3期614-622,共9页
The reverse transcription quantitative real-time PCR(RT-qPCR) has become one of the most important techniques of studying gene expression. A set of valid reference genes are essential for the accurate normalization of... The reverse transcription quantitative real-time PCR(RT-qPCR) has become one of the most important techniques of studying gene expression. A set of valid reference genes are essential for the accurate normalization of data. In this study, five candidate genes were analyzed with ge Norm, Norm Finder, Best Keeper and ?Ct methods to identify the genes stably expressed in echiuran Urechis unicinctus, an important commercial marine benthic worm, under abiotic(sulfide stress) and normal(adult tissues, embryos and larvae at different development stages) conditions. The comprehensive results indicated that the expression of TBP was the most stable at sulfide stress and in developmental process, while the expression of EF-1-α was the most stable at sulfide stress and in various tissues. TBP and EF-1-α were recommended as a suitable reference gene combination to accurately normalize the expression of target genes at sulfide stress; and EF-1-α, TBP and TUB were considered as a potential reference gene combination for normalizing the expression of target genes in different tissues. No suitable gene combination was obtained among these five candidate genes for normalizing the expression of target genes for developmental process of U. unicinctus. Our results provided a valuable support for quantifying gene expression using RT-qPCR in U. unicinctus. 展开更多
关键词 reference gene RT-Qpcr sulfide stress TISSUE developmental process Urechis unicinctus
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白色链霉菌JA3453中垩唑霉素生物合成基因簇调节基因的中断研究
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作者 宋丹凤 赵春华 邓子新 《上海交通大学学报(农业科学版)》 2008年第3期247-250,共4页
通过生物信息学分析,在白色链霉菌JA3453菌株的垩唑霉素生物合成基因簇中定位了2个调节基因。其中1个是属于LysR家族的调控因子编码基因ozmR,另1个为编码转录激活因子基因ozmU。为了研究这2个调节基因的功能,选用垩唑霉素的产生菌链霉菌... 通过生物信息学分析,在白色链霉菌JA3453菌株的垩唑霉素生物合成基因簇中定位了2个调节基因。其中1个是属于LysR家族的调控因子编码基因ozmR,另1个为编码转录激活因子基因ozmU。为了研究这2个调节基因的功能,选用垩唑霉素的产生菌链霉菌JA3453为实验材料,采用目标PCR的方法,对调节基因ozmR和ozmU分别进行基因中断。HPLC-MS分析显示,ozmR的中断可以提高垩唑霉素的产量,ozmU的中断则没有对垩唑霉素的产量带来明显影响。这些结论为利用调节基因提高垩唑霉素的产量提供了可能。 展开更多
关键词 目标pcr 调节基因 基因中断 垩唑霉素
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