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胡枝子属ISSR-PCR反应体系的建立与优化 被引量:16

Establishment and Optimization of ISSR Reaction System for Lespedeza spp.
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摘要 在利用ISSR技术对胡枝子属种质资源遗传多样性进行研究的实验过程中,对影响PCR扩增效果的一些因素如DNA的提取、模板DNA质量浓度、Taq酶用量、引物用量、dNTP的用量以及退火温度等指标进行筛选和优化,筛选优化出可用于胡枝子属ISSR-PCR分析较适宜的PCR反应条件:Taq酶1.0 U,2μL的10×Buffer(200 mM Tris-HC l;200 mM KC l;100 mM(NH4)2SO4;15 mM MgC l2),模板DNA 40 ng,dNTP 0.2 m mol/L,引物0.2μmol/L. The influencing factors including genomic DNA extraction, concentration of template DNA, dosage of Taq DNA polymerase, primer concentration, dNTP dosage and the annealing temprature upon the amplification effect with PCR technique were studied for optimizing the ISSR reaction conditions for studies on the genetic diversity of Lespedeza spp. germplasm resources. The results showed that the optimum reaction conditions for ISSR PCR of Lespedeza spp. were as follows:1. 0 U Taq DNA(produeed by TIANWEI company) + 2 μL 10 ×Taq buffer (200 mM Tfis -HCl; 100 mM (NH4)2SO4 ;200 mM KC1 ;15 mM MgCl2) + 40 ng template DNA +0. 2 m mol/L L dNTP + 0. 2 μmol/L primer.
出处 《西南林学院学报》 CAS 2006年第2期6-9,23,共5页 Journal of Southwest Forestry College
基金 国家高新技术研究发展计划(863)资助项目(2002AA241111)
关键词 胡枝子属 ISSR-PCR 反应体系 Lespedeza spp. ISSR - PCR reaction conditions
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