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

蝴蝶兰SRAP反应体系的建立与优化
引用本文:杨珺,任羽,杨光穗,尹俊梅.蝴蝶兰SRAP反应体系的建立与优化[J].热带农业科学,2010,30(3):21-24.
作者姓名:杨珺  任羽  杨光穗  尹俊梅
作者单位:1. 中国热带农业科学院热带作物品种资源研究所,海南儋州,571737;海南大学农学院,海南儋州,571737
2. 中国热带农业科学院热带作物品种资源研究所,海南儋州,571737;农业部热带作物种质资源利用重点开放实验室,海南儋州,571737
基金项目:科技部国家科技支撑计划项目,海南省重大科技研发专项,海南省自然科学基金 
摘    要:以蝴蝶兰嫩叶提取的DNA为材料,蝴蝶兰SRAP反应体系中的重要参数Mg2+、Taq酶、模板DNA及随机引物,建立了一套适合蝴蝶兰基因扩增的SRAP反应体系:25μL的反应体系中Mg2+浓度为2.0mmol/L,Taq酶1.0U,DNA模板40ng,上下游引物0.8mmol/L。该体系扩增条带清晰,重复性好,有望在蝴蝶兰属植物的遗传育种研究中运用。

关 键 词:蝴蝶兰  SRAP反应体系  优化

Establishment and Optimization of Sequence-Related Amplified Polymorphism System for Phalaenopsis
YANG Jun,REN Yu,YANG Guangsui,YIN Junmei.Establishment and Optimization of Sequence-Related Amplified Polymorphism System for Phalaenopsis[J].Chinese Journal of Tropical Agriculture,2010,30(3):21-24.
Authors:YANG Jun  REN Yu  YANG Guangsui  YIN Junmei
Institution:1 Tropical Crops Genetic Resources Institute,CATAS,Danzhou,Hainan 571737;2 College of Agronomy,Hainan University,Danzhou,Hainan 571737;3 Ministry of Agriculture Key Laboratory of Tropical Crop Germplasm Resources Utilization,Danzhou,Hainan 571737)
Abstract:The DNA from the Phalaenopsis tender leaves was used as the experimental material.In order to establish the optimized SRAP detection system,the concentrations of Mg2+,Taq DNA polymerase,template DNA and the random primers were optimized for SRAP-PCR reaction.The optimal conditions were 2.0 mmol/L Mg2+,1.0 U Taq DNA polymerase,40 ng template DNA,0.8 mmol/L upstream primer and downstream primer.The amplified bands were clear and had good reproducibility,thus the optimized SRAP detection system could be used for the study on molecular markers of Phalaenopsis.
Keywords:Phalaenopsis aphrodita Rchb  f    SRAP reaction system  optimization
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