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Construction of an Internal Control to Quantitate Multiple Porcine Cytokine mRNAs by RT-PCR

机译:通过RT-PCR定量多个猪细胞因子mRNA内部控制的构建

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A multiple internal control was constructed to be used as an exogenously added control in reverse transcription polymerase chain reaction (RT-PCR) for pig cytokines. It consists of 5' and 3' primer sequences in the order of β_2 microglobulin (β_2-m)> IL-1, IL-4, IL-6, IL-8, IL-2, IL-10, TNF-α, TNF-β andIFN-γ. Construction was accomplished by overlapping and extension PCR (OE-PCR) utilizing short oligonucleotides. The primers were designed to give two products of different sizes on co-amplification of control and target RNAs by RT-PCR in a single tube. This permits analysis of message for several cytokines using a single exogenously added competitive template. Incorporated endonuclease sites allow construct modification by oligonucleotide addition.
机译:构建了多个内部对照,用作猪细胞因子的逆转录聚合酶链反应(RT-PCR)中的外源添加对照。它由按照β_2微球蛋白(β_2-m)> IL-1,IL-4,IL-6,IL-8,IL-2,IL-10,TNF-α, TNF-β和IFN-γ。通过使用短寡核苷酸的重叠和延伸PCR(OE-PCR)完成构建。设计引物以在单个管中通过RT-PCR共扩增对照RNA和靶RNA时得到两种大小不同的产物。这允许使用单个外源添加的竞争模板来分析几种细胞因子的信息。结合的核酸内切酶位点允许通过添加寡核苷酸来修饰构建体。

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