大豆中转基因成分的定性PCR检测.doc

  • 需要金币1000 个金币
  • 资料包括:完整论文
  • 转换比率:金钱 X 10=金币数量, 即1元=10金币
  • 论文格式:Word格式(*.doc)
  • 更新时间:2014-07-12
  • 论文字数:5216
  • 当前位置论文阅览室 > 论文模板 > 农业论文 >
  • 课题来源:(圈圈)提供原创文章

支付并下载

摘 要:目的:从转基因大豆中提取DNA并对大豆中转基因成分进行检测。方法:CTAB法、PCR扩增技术、设计并合成引物对转基因大豆的内源基因Lectin;外源基因CaMV35S 启动子、NOS终止子和Cp4 EPSPS基因进行检测。结果:转基因大豆中含有内源基因Lectin;外源基因CaMV35S 启动子、NOS终止子和Cp4 EPSPS基因。

关键词:转基因大豆;转基因成分定性PCR检测;Lectin基因;CaMV35S基因;Cp4 EPSPS基因

 

Abstract:Objective: To extract DNA from genetically modified soybean and to detect Genetically Modified Components in Soybean. Methods: DNA was extracted from soybean by CTAB method, the technique of PCR amplification, The primers for endogenous gene Lectin of genetically modified soybean, CaMV35S promoter gene , NOS terminator and Cp4 epsps gene were designed and synthesized. Results: There are endogenous gene Lectin , CaMV35S promoter gene , NOS terminator and Cp4 epsps gene in genetically modified soybean.

Key words:genetically modified soybean; qualitative PCR detection of genetically modified organisms; Lectin gene; CaMV35Sgene; Cp4 EPSPS gene.