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桃SRAP-PCR反应体系的建立与优化
引用本文:史红丽,韩明玉,赵彩平.桃SRAP-PCR反应体系的建立与优化[J].华北农学报,2008,23(Z2).
作者姓名:史红丽  韩明玉  赵彩平
作者单位:西北农林科技大学,园艺学院,陕西,杨陵,712100
基金项目:陕西省攻关项目(2006K01-G27-01); 农业部“948”项目(2006-G27)
摘    要:建立适宜桃基因组DNA的SRAP-PCR扩增体系,为桃基因图谱的构建和分子标记打下基础。以桃基因组DNA为模板,通过正交试验设计,从dNTPs、Mg2+、Taq酶、引物、模板5种因素4个水平对桃SRAP-PCR反应体系进行优化,所建立的体系为25μL:dNTPs为0.12 mmol/L,Mg2+为4 mmol/L,Taq酶2 U,引物为0.3 mmol/L,模板DNA50ng。PCR反应程序为:94℃预变性5 min;94℃变性l min,35℃复性l min,72℃延伸l min,5个循环;94℃变性l min,50℃复性l min,72℃延伸l min,35个循环,72℃延伸10 min。

关 键 词:  SRAP  优化  正交试验  

Optimization of SRAP Reaction System in Peach(Prunus persica)
SHI Hong-li,HAN Ming-yu,ZHAO Cai-ping.Optimization of SRAP Reaction System in Peach(Prunus persica)[J].Acta Agriculturae Boreali-Sinica,2008,23(Z2).
Authors:SHI Hong-li  HAN Ming-yu  ZHAO Cai-ping
Abstract:The aim of the research was to establish SRAP-PCR amplification system which was suitable for Peach(Prunus persica) genome DNA so as to lay foundation for the construction of gene map and molecular marker in Peach(Prunus persica).Peach(Prunus persica) genome DNA as template,the major components of SRAP,such as concentrations of dNTPs,Mg2+,Taq DNA polymerase,primers and template,were optimized in this study by orthogonal design in five factors four levels respectively.The results showed that the optimum SRAP...
Keywords:SRAP
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