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家蚕来源肠球菌RAPD反应体系的优化
引用本文:宋连花,王彦文,牟志美,黄艳红. 家蚕来源肠球菌RAPD反应体系的优化[J]. 河北林果研究, 2006, 21(1): 78-81
作者姓名:宋连花  王彦文  牟志美  黄艳红
作者单位:1. 山东农业大学,林学院,山东,泰安,271018
2. 山东农业大学,林学院,山东,泰安,271018;四川农业大学,动物科技学院,四川,雅安,625014
基金项目:国家茧丝绸发展风险基金
摘    要:
通过调整 Mg2 、DNA模板、引物、Taq DNA聚合酶和dNTPs的浓度及PCR反应循环次数,建立并优化了家蚕来源肠球菌的RAPD-PCR反应体系及条件.结果表明,在25 μl反应体系下,当Mg2 的浓度为3.5 mmol/L、DNA模板加入量为50 ng、引物浓度为15 pmol/L、Taq DNA聚合酶加入量为3U、 PCR反应循环次数为45时,扩增结果最好.在本实验室,为家蚕来源肠球菌的遗传多样性研究建立了一种最佳RAPD分析模型.

关 键 词:家蚕  肠球菌  随机扩增DNA多态性分析  条件优化
文章编号:1007-4961(2006)01-0078-04
修稿时间:2005-11-08

Optimization on the conditions of RAPD analysis in enterococci isolated from Bombyx mori
SONG Lian-hua,WANG Yan-wen,MU Zhi-mei,HUANG Yan-hong. Optimization on the conditions of RAPD analysis in enterococci isolated from Bombyx mori[J]. Hebei Journal of Forestry and Orchard Research, 2006, 21(1): 78-81
Authors:SONG Lian-hua  WANG Yan-wen  MU Zhi-mei  HUANG Yan-hong
Abstract:
The influences of concentration of Mg~(2 ),DNA template,primer,T(aq) polymerase,dNTPs and number of cycles had been tested for the amplification of random amplified polymorphic DNA(RAPD) in Enterococci of Bombyx mori. The results showed that when Mg~(2 ) at 3.5 mmol/L,DNA template at 50 ng,primer at 15 pmol/L,T(aq) polymerase at 3U,dNTPs at 200 mmol/L and the number of cycles was 45,the amplification performed perfectly.An optimization RAPD analysis pattern for the genetic research in Enterococci of Bombyx mori was established.
Keywords:Bombyx mori  Enterococci  random amplified polymorphic DNA(RAPD)  conditions optimization
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