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Cana Cloning and Plant Expression Vector Construction of Soybean 11s Glycerin Gy3

机译:大豆11s甘油Gy3的Cana克隆及植物表达载体的构建

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The RNA was extracted from immature seeds of soybean and it is directly used in single-stranded dank synthetic reaction. According to soybean 11s glycerin Gy3 coda sequences in gene bank, a pair of primers was designed. Double-stranded coda was amplified by PCR. The amplified Gy3 coda was cloned into plasmid pMD19-T and sequenced. Fragment of the Gy3 coda in the recombi-nant plasmid was cut with Xbox Ⅰ/bah I and ligated with plasmid pbi121, and then a plant expression vector was constructed. It includes camv35 proctor, nose terminator and no-Ⅱ gene.
机译:RNA是从大豆的未成熟种子中提取的,可直接用于单链潮湿的合成反应中。根据基因库中大豆11s甘油Gy3的编码序列,设计了一对引物。通过PCR扩增双链尾气。将扩增的Gy3尾气克隆到质粒pMD19-T中并测序。用XboxⅠ/ bah I切割重组质粒中的Gy3尾片段,并与质粒pbi121连接,然后构建植物表达载体。它包括camv35启动子,鼻终止子和no-Ⅱ基因。

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