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利用MPCR技术快速检测进口大豆转基因背景
引用本文:徐景升,余爱丽,姚伟,饶进,张木清,陈如凯. 利用MPCR技术快速检测进口大豆转基因背景[J]. 江西农业大学学报, 2005, 27(2): 262-264,269
作者姓名:徐景升  余爱丽  姚伟  饶进  张木清  陈如凯
作者单位:福建农林大学,农业部甘蔗生理生态与遗传改良重点开放实验室,福建,福州,350002
基金项目:福建省重大国际合作项目(2001I002),948项目“甘蔗良种和技术引进与推广”(2003-Q06),863高新技术发展计划课题(2001AA241191)
摘    要:利用改良的CATB方法提取大豆(Glycine max)种子基因组DNA。以大豆内源ScII基因做对照,采用MPCR(Multiplex Polymerase Chain Reaction,MPCR)技术从进口大豆中检测出35S启动子、NOS终止子和EPSPS耐除草剂基因3种转基因成分。

关 键 词:MPCR 转基因 大豆 检测
文章编号:1000-2286(2005)02-0262-03

Rapid Detection of Imported Genetically Modified Soybean (Glycine max) with MPCR
XU Jing-sheng,YU Ai-li,YAO Wei,Rao Jin,ZHANG Mu-qing,CHEN Ru-kai. Rapid Detection of Imported Genetically Modified Soybean (Glycine max) with MPCR[J]. Acta Agriculturae Universitis Jiangxiensis, 2005, 27(2): 262-264,269
Authors:XU Jing-sheng  YU Ai-li  YAO Wei  Rao Jin  ZHANG Mu-qing  CHEN Ru-kai
Abstract:The DNA was successfully extracted from soybean(Glycine max) seeds by a modified CTAB method. Three transgenic elements, 35S promoter, NOS terminator and EPSPS (5-enolpyruvylshikimate-3- phosp-hate synthase), were detected in the imported soybean seeds by MPCR(Multiplex Polymerase Chain Reaction,MPCR) with the ScII as the control.
Keywords:MPCR  transgenic  soybean(Glycine max)  detection
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