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梓树属植物基因组DNA提取及RAPD体系优化
引用本文:王念,王巧玲.梓树属植物基因组DNA提取及RAPD体系优化[J].河南林业科技,2012(1):1-3.
作者姓名:王念  王巧玲
作者单位:1. 河南省林木良种选育与种质资源保护重点实验室,郑州,450008
2. 河南省林业调查规划院,郑州,450045
基金项目:国家林业局“十二五”科技支撑项目(编号:2012BAD01805)
摘    要:以楸树幼嫩叶片为材料,进行楸树基因组DNA提取及RAPD扩增条件优化,试验表明,采用改良的2×CTAB法提取的DNA质量较高,适宜于RAPD分析。RAPD反应的优化体系为(25 ul反应体系):17.8 ul ddH2O;0.5 ul dNTP;2.5 ul 10×buffer;1.0 ul随机引物;2.0 ul Mgcl2;1.0 ul模版;0.2 ul Taq酶。

关 键 词:楸树  DNA提取  RAPD

Genomic DNA Extraction and Optimization of RAPD System of Catalpa Scop
WANG Nian,WANG Qiao-ling.Genomic DNA Extraction and Optimization of RAPD System of Catalpa Scop[J].Journal of Henan Forestry Science and Technology,2012(1):1-3.
Authors:WANG Nian  WANG Qiao-ling
Institution:1.Key Laboratory of Forest Germplasm Conservation. Breeding of Improved Variety of Henan-Province,Zhengzhou 450008, China; 2. Henan Forest Inventory and Planning Institute, Zhengzhou 450045, China)
Abstract:The method of genomic DNA extraction from new leaves and the optimization of RAPD analytic conditions were studies in Catalpa bungei. The result showed that the high-quality genomic DNA wasobtained by the revised 2 × CTAB method. The optimal PCR system for RAPD analysis was as foUows:17.6ul ddH2O;0.5ul dNTP;2.5ul 10× buffer; 1.01ul random Primer;2.0ul Mgcl2;1.0ul template;0.4ul Taq polymerase in 25ul reaction system.
Keywords:Catalpa bungei  Genomic DNA extraction  RAPD
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