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作 者:张伟[1] 谢甫绨[1] 宋显军[1] 曹萍[1] 郭玉华[1]
出 处:《华北农学报》2007年第2期133-135,共3页Acta Agriculturae Boreali-Sinica
基 金:国家"948"计划项目(2003-Q04)
摘 要:为了探寻大豆干种子中的DNA快速提取方法,以2个大豆品种的干种子为材料,在SDS提取液中加入蛋白酶K、NP-40、Tween-20情况下,并减少氯仿/异戊醇的抽提次数,研究对提取DNA质量的影响。结果表明,SDS提取液中加入3种试剂后,即使使用氯仿/异戊醇抽提1次,其DNA的0D260/0D280值也在1.8—2.0之间,能够满足SSR扩增模板的需求。说明此方法既可获得较高纯度的DNA,又可大大缩短大豆干种子中的DNA提取时间。To develop a rapid DNA extraction method, the quality of DNA was examined with soybean dry seeds as materials, adding proteinase K, NP-40 and Tween-20 to SDS extracting solution, and reducing the chlorofonn/isoamyl extraction times. The results showed that when adding the three reagents to SDS extracting solution, the OD260/OD280 value of DNA was between 1.8 and 2.0 even extracted once by chlorofonn/isoamyl. Thus, good quality and quantity template DNA suitable for SSR analysis was obtained with reduced time.
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