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北沙参SRAP分子标记体系的建立与优化
引用本文:齐树杰,沈 镝,李 颖,张钦德,李庆典.北沙参SRAP分子标记体系的建立与优化[J].中国农学通报,2009,25(24):73-77.
作者姓名:齐树杰  沈 镝  李 颖  张钦德  李庆典
作者单位:1. 青岛农业大学,山东,青岛,266109
2. 中国农业科学院,北京,100850
3. 山东中医药高等专科学校,山东,烟台,264000
基金项目:国家中医药局课题"北沙参道地药材质量标准规范化研究" 
摘    要:为北沙参的遗传多样性分析提供一种科学的途径。采用SRAP标记技术,以北沙参基因组DNA为模板,优化了SRAP反应体系的各主要参数。建立了稳定可靠的SRAP-PCR反应体系;20μL反应体系中,DNA的量为80ng、Mg2+ 2.5mmol/L、dNTPs 0.25mmol/L、TaqDNA聚合酶为1U、正反向Primer浓度均为0.1μmol/L。该体系适合北沙参遗传多样性分析、遗传图谱构建等研究。

关 键 词:粮草间作  粮草间作  坡耕地  培肥保土  效益  
收稿时间:2009-08-13
修稿时间:2009-09-03

Establishment and Optimization of SRAP Reaction System in Glehnia littoralis
Qi Shujie,Shen Di,Li Ying,Zhang Qinde,Li Qingdian.Establishment and Optimization of SRAP Reaction System in Glehnia littoralis[J].Chinese Agricultural Science Bulletin,2009,25(24):73-77.
Authors:Qi Shujie  Shen Di  Li Ying  Zhang Qinde  Li Qingdian
Institution:Qi Shujie, Shen Di, Li Ying, Zhang Qinde, Li Qingdian (1Qingdao Agricultural University, Qingdao Shandong 266109; 2Chinese Academy of Agricultural Sciences, Beijing 100850; 3Shandong College of Traditional Chinese Medicine, Yantai Shandong 264000)
Abstract:To develop a sicentific method for Glehnia litteralis genetic diversity analysis. Glehnia litteralis DNA was used to optimize SRAP system’s main parameters. A stability and reliable SRAP-PCR system was established. In the 20μL system, DNA 80 ng, Mg2+ 2.5 mmol/L, dNTP 0.25mmol/L, Taq 1U, Upstream and Downstream primers both for 0.25μmol/L. The reaction system was suitable to study Glehnia litteralis genetic diversity analysis and gene mapping.
Keywords:Glehnia litteraliszz  SRAPzz  molecular markerzz  system optimizationzz
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