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麻疯树cpSSR标记技术的建立与体系优化研究
引用本文:向倩,周兰英,万静,张旭,雷宝盛,金银春,冯毅,赵晓英,于绪任. 麻疯树cpSSR标记技术的建立与体系优化研究[J]. 安徽农业科学, 2009, 37(32): 15746-15748
作者姓名:向倩  周兰英  万静  张旭  雷宝盛  金银春  冯毅  赵晓英  于绪任
作者单位:四川农业大学林学院,四川雅安,625014 
摘    要:
[目的]建立麻疯树cpSSR—PCR反应的最佳反应体系。[方法]对影响麻疯树cpSSR—PCR反应体系的5个因素(细DNA聚合酶、DNA模板、Mg2+、dNTP、引物)进行优化试验,筛选各反应因素的最佳水平。[结果]20山反应体系各组分的最合适浓度分别为10XBuffer、2.00mmoL/LMg2+、2U/μlTagDNA聚合酶、0.2mmol/LdNTP、0.2μmol/L引物、35ng/μlDNA模板。[结论]最佳的退火温度为52℃:该反应体系的稳定性和可重复性均较好。

关 键 词:麻疯树  cpSSR—PCR  体系优化

Study on Establishment of cpSSR Marker Technology and Optimization of Its Reaction System in Jatropha curcas Linn
XIANG Qian et al. Study on Establishment of cpSSR Marker Technology and Optimization of Its Reaction System in Jatropha curcas Linn[J]. Journal of Anhui Agricultural Sciences, 2009, 37(32): 15746-15748
Authors:XIANG Qian et al
Affiliation:XIANG Qian et al (College of Forestry , Horticulture,Sichuan Agricultural University,Yaan,Sichuan 625014)
Abstract:
[Objective] The aim was to build an optimal cpSSR-PCR system for Jatropha curcas Linn. [Method] Optimize cpSSR-PCR amplification system for Jatropha curcas Linn in terms of five factors( Taq DNA polymerase, Mg~(2+), DNA template, dNTP and primer)from several levels. [Result] An optimal cpSSR-PCR system for Jatropha curcas Linn was obtained as 2.00 mmol/L Mg~(2+), 2 U/μl Taq DNApolymerase, 0.2 mmol/L dNTP, 0.2 μmol/L Primer, 35 ng/μl DNA template for 20 μl reaction syetem. [Conclusion] The optimal annealing temperature for cpSSR-PCR reaction syetem is determined as 52 ℃. The cpSSR reaction system was steady and reproducible.
Keywords:cpSSR-PCR  Jatropha curcas Linn  cpSSR marker  Optimization of reaction system
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