首页 | 本学科首页   官方微博 | 高级检索  
     

麻疯树cpSSR标记技术的建立与体系优化
引用本文:向倩,周兰英,万静,张旭,雷宝盛,金银春,冯毅,于绪任,赵晓英. 麻疯树cpSSR标记技术的建立与体系优化[J]. 农业科学与技术, 2009, 10(4): 61-64,74
作者姓名:向倩  周兰英  万静  张旭  雷宝盛  金银春  冯毅  于绪任  赵晓英
作者单位:四川农业大学林学院,四川雅安,625014 
基金项目:National Scientific and Technical Supporting Project of Studies on Superior Species Selecting and Breeding Technique of Jatropha curcas Linn (2007BAD50B01).国家科技支撑课题"麻疯树高油、高产、多抗性良种选育技术研究" 
摘    要:1材料与方法1.1材料采自我国西南10个地区的麻疯树野生居群的枝条扦插(表1),摘取幼叶用于提取总DNA。

关 键 词:SSR标记技术  麻疯树  优化  cp  枝条扦插  野生居群  总DNA  材料

Study on Establishment of cpSSR Marker Technology and Optimization of Its Reaction System in Jatropha curcas Linn
XIANG Qian,ZHOU Lan-ying,WAN Jing,ZHANG Xu,LEI Bao-sheng,JIN Yin-chun,FENG Yi,YU Xu-ren,ZHAO Xiao-ying. Study on Establishment of cpSSR Marker Technology and Optimization of Its Reaction System in Jatropha curcas Linn[J]. Agricultural Science & Technology, 2009, 10(4): 61-64,74
Authors:XIANG Qian  ZHOU Lan-ying  WAN Jing  ZHANG Xu  LEI Bao-sheng  JIN Yin-chun  FENG Yi  YU Xu-ren  ZHAO Xiao-ying
Affiliation:(Forestry College of Sichuan Agricultural University, Ya'an 625014)
Abstract:[ Objective] The aim of this study was to establish the optimum cpSSR-PCR system for Jatropha curcas Linn. [ Method] cpSSR-PCR amplification system for Jatropha curcas Linn influenced by five factors including Taq DNA polymerase, Mg^2+ , DNA template, dNTP and primer were optimized from several levels. [ Result] The optimum concentration of 20 μl reaction system was 10 × Buffer, 2.00 mmol/L Mg^2+ , 2 U/μl Taq DNA polymerase, 0.2 mmol/L dNTP, 0.2 μmol/L primer and 35 ng/μl DNA template. [ Conclusion] The optimum annealing temperature for cpSSR-PCR reaction system is 52 ℃, and the cpSSR reaction system is steady and reproducible.
Keywords:Jatropha curcas Linn  cpSSR-PCR  Optimization of reaction system
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号