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荔枝DNA提取及RAPD扩增条件优化
引用本文:尤有利,王江波,施维属,潘东明.荔枝DNA提取及RAPD扩增条件优化[J].生物技术通报,2010(4).
作者姓名:尤有利  王江波  施维属  潘东明
作者单位:1. 福建永春县农业技术推广站,泉州,362600
2. 福建农林大学园艺学院,福建农林大学园艺产品贮运保鲜研究所,福州,350002
基金项目:泉州市科技计划项目,我国台湾农业新品种、新技术引进创新研究与示范项目,我国台湾果树新品种与品质控制新技术引进创新研究项目 
摘    要:为应用RAPD技术开展对荔枝种质资源的分析,以S43(GTCGCCGTCA)为引物,通过试验设计,分别研究了退火温度、模板浓度、引物浓度、dNTP浓度、Taq DNA聚合酶用量对荔枝RAPD-PCR反应的影响。建立并优化了适宜荔枝RAPD分析的扩增体系:20μL的反应体系,30ng的模板DNA度,0.25μmol/LRAPD引物、1.0UTaqDNA聚合酶,0.2μmol/LdNTP为荔枝适宜的RAPD-PCR扩增条件。

关 键 词:荔枝  优化

Extration of Genomic DNA of Litchi chinensis and Optimizationof the RAPD Reaction System
You Youli,Wang Jiangbo,Shi Weishu,Pan Dongming.Extration of Genomic DNA of Litchi chinensis and Optimizationof the RAPD Reaction System[J].Biotechnology Bulletin,2010(4).
Authors:You Youli  Wang Jiangbo  Shi Weishu  Pan Dongming
Institution:You Youli1Wang Jiangbo2Shi Weishu2Pan Dongming2(1 Yongchun Agro-Techinical Extension Station,Quanzhou 362600,2College of Horticulture,Fujian Agriculture , Forestry University,Institute of Storage Science , Technology ofHorticultural Products,Fuzhou 350002)
Abstract:In order to use RAPD markers to analyze the resources in Litchi,the annealing temperature, template,concentration of primer, dNTP and the Taq DNA polymerase dosage on RAPD-PCR applications were tested to determine their optimal level . Besides,the following optimal reaction system for RAPD analysis in Litchi were established,including PCR reaction volume of 20 μL,30 ng DNA template,0.25 μmol/L RAPD primer,1.0 U Taq DNA polymerase,and 0.2 μmol/L dNTP in each reaction system of 20 μL.
Keywords:RAPD  PCR  Litchi chinensis  Sonn  RAPD  Optimize  PCR
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