首页 | 本学科首页   官方微博 | 高级检索  
     检索      

苹果自交不亲和基因PCR扩增程序优化
引用本文:陈超,于葆杰,李保国.苹果自交不亲和基因PCR扩增程序优化[J].天津农业科学,2009,15(4):24-26.
作者姓名:陈超  于葆杰  李保国
作者单位:1. 河北省沧州市林业科学研究所,河北,沧州,061000
2. 河北农业大学,林学院,河北,保定,071000
摘    要:通过研究PCR反应体系(DNA、Primer、Mg2+、dNTP、Taq聚合酶、buffer)及退火温度对苹果自交不亲和基因(S基因)扩增结果影响的分析,构建了适合于苹果自交不亲和基因的PCR扩增程序的优化体系。结果表明:在20μL的反应体系中,模板DNA的最适含量为40ng,dNTP最适浓度为0.25mmol/L,而Primer最适浓度为0.4μmol/L,Mg2+的最适浓度为2.5mmol/L,Taq聚合酶最适浓度为1U,buffer最适浓度为1×buffer,最适退火温度为50℃。

关 键 词:苹果  S基因  PCR体系优化

Optimized Study on PCR Amplification Procedure of the Apple Self-incompatibility Gene
CHEN Chao,YU Bao-jie,LI Bao-guo.Optimized Study on PCR Amplification Procedure of the Apple Self-incompatibility Gene[J].Tianjin Agricultural Sciences,2009,15(4):24-26.
Authors:CHEN Chao  YU Bao-jie  LI Bao-guo
Institution:CHEN Chao, YU Bao-jie, LI Bao-guo (1.Forestry Science Institute of Cangzhou, Cangzhou, Hebei 061001, China; 2. Forestry College, Hebei Agricultural University, Baoding, Hebei 071000, China)
Abstract:Through analyzing the effect of PCR system (DNA, Primer, Mg^2+, dNTP, Taq polymerase, and buffer) and annealing temperature on amplification of apple self-incompatibility gene (s-gene), we constructed a optimized system of PCR amplification procedure which was fit for apple self-incompatibility gene. The result showed that the optimized content in 20 μL system contained 40 ng DNA template, 0.25 mmol/L dNTP, 0.4 μmol/L primer, 2.5 mmol/L Mg^2+, 1 U Taq polymerase, lxbuffer, and the optimized annealing temperature was 50 ℃.
Keywords:apple  s-gene  optimized PCR 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