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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克隆和植物表达载体施工

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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:从大豆的未成熟种子中萃取RNA,直接用于单链的陷阱合成反应。根据大豆11S甘油Gy3 Coda序列在基因库中,设计了一对引物。通过PCR扩增双链CoDa。将扩增的GY3 CODA克隆到质粒pMD19-T中并进行测序。用XboxⅠ/ BAH I切割重组Ⅰ/ BAH I中GY3 CODA的片段并用质粒PBI121连接,然后构建植物表达载体。它包括CAMV35标准器,鼻终止剂和NO-Ⅱ基因。

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