摘要
对佛手DNA提取过程从不同方面进行了改良、优化 ,筛选出较理想的佛手DNA提取方法 :每eppen dorf管鲜样品取量为 0 .1g~ 0 .2 5 g ,70 0 μL提取缓冲液 ,加提取液前用液氮研磨 ,Vc(抗坏血酸 )添加量为w(VC/鲜样 ) =0 .1.该方法分离出DNA的A2 60 /A2 80 大于 1.9,符合佛手RAPD(随机扩增多态DNA)分析要求 ,在佛手遗传多态性分析和品种分子鉴定中具有良好的应用前景 .
It was improved and optimized by the authors the course of bergamot DNA extraction from different aspects,filtrated an ideal bergamot DNA extraction method [0.1 g~0.25 g fresh sample,700 μL extraction buffer, liquid nitrogen whet,w(Vc/ fresh sample)=0.1].The A-{260}/A-{280} values of isolated DNA was above 1.9. This method coincided with the requisition of RAPD analysis, and was promising for bergamot genetic polymorphism analysis and cultivar identification.
出处
《浙江师范大学学报(自然科学版)》
CAS
2002年第1期52-55,共4页
Journal of Zhejiang Normal University:Natural Sciences