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转基因杨树外源基因PCR检测模板DNA的快速制备

A rapid preparation of template DNA for PCR detection of extraneous genes of transgenic Populus tomentosa
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摘要 用带盖离心管定量取转基因毛白杨组培苗及其室外8 a生植株叶片,加入DNA提取缓冲液研磨,离心后取上清液稀释5倍。取1μL作为PCR模板DNA检测杨树外源Bt和Npt II基因。PCR产物经琼脂糖凝胶电泳检测,目的条带清晰,可重复性强。 The leaves of tissue culture stocks and of 8 years old trees of transgenie Populus tomentosa were taken as materials using centrifuge tube. The materials were grinded for 15 - 20 s with DNA extraction buffer at room temperature. Samples were centrifuged,and the supematants of 5- fold diluted were used as a PCR template DNA to detect the Bt gene and the Npt II gene.
出处 《河北林果研究》 2009年第4期349-352,共4页 Hebei Journal of Forestry and Orchard Research
基金 河北省科技厅资助项目(03547016D) 河北省林业局资助项目(0207216)
关键词 转基因毛白杨 模板DNA制备 PCR检测 transgenic Populus tomentosa preparation of template DNA PCR detection
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