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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, 0(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, 0(4)
Authors:You Youli  Wang Jiangbo  Shi Weishu  Pan Dongming
Affiliation: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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