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Real-time PCR data for reference candidate gene selection in tomato infected with Tomato curly stunt virus

机译:用于参考候选基因选择的实时PCR数据用番茄卷曲特技病毒感染番茄

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Real-time PCR (qPCR) is a useful and robust method of quantifying gene expression, provided that suitable reference genes are used to normalize the data. To date, suitable reference genes have not been validated for tomato gene expression changes in response to Tomato curly stunt virus (ToCSV). RT-qPCR was conducted on resistent (R) and susceptible (S) tomato leave tissue infected with ToCSV at 35 days post infection. Ten candidate reference genes were selected and validated using SYBR green. Here, we report a set of primers designed for the ten candidate genes and the data for the melt curve analysis and standard curves generated for each candidate reference gene. This data provides a useful resourse in reference gene selection for future use in the normalization of qPCR data investigating tomato-virus interactions. To our knowledge, this data provides the first selection and testing of candidate reference genes in a tomato-ToCSV pathosystem.
机译:实时PCR(QPCR)是定量基因表达的有用且鲁棒的方法,但是提供了合适的参考基因来标准化数据。迄今为止,尚未验证合适的参考基因以促进番茄卷曲特技病毒(TOCSV)的番茄基因表达变化。 RT-QPCR在感染后35天在35天内感染TOCSV感染的抗毒性(r)和易感番茄植物。使用Sybr Green选择并验证了十个候选参考基因。在这里,我们报告了一组设计用于十个候选基因的引物和用于对每个候选参考基因产生的熔融曲线分析和标准曲线的数据。该数据在参考基因选择中提供了有益的资益,以便在调查番茄病毒相互作用的QPCR数据的正常化中使用。据我们所知,该数据提供了番茄 - TOCSV Pathosystem中候选参考基因的第一个选择和测试。

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