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拟南芥AtNHX1基因克隆和cre(lox)植物表达载体构建 被引量:7

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摘要 从拟南芥叶片提取总RNA,经反转录得到cDNA。根据Genbank数据库中已登记的拟南芥Na+/H+逆向转运蛋白基因AtNHX1的核苷酸序列设计并合成了1对克隆引物,通过PCR方法从cDNA中扩增出AtNHX1基因片段,将该目的片段克隆至pGEM-TEazy载体。通过酶切,从pGEM-TEazy载体上切下目的基因片段,替换pX6-GFP载体中的GFP基因,构建了AtNHX1基因cre/lox植物表达载体。
出处 《江苏农业科学》 CSCD 北大核心 2007年第6期348-350,共3页 Jiangsu Agricultural Sciences
基金 南京晓庄学院生态学校级重点学科项目(编号:2005-2008) 南京晓庄学院科研启动基金(编号:4051065) 南京晓庄学院重点项目(编号:2007NXY10)
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参考文献6

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二级参考文献33

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