作 者: ; ; ; (颜彤); (欧阳炜); (刘雁彬); (努尔亚);
机构地区: 西北农林科技大学
出 处: 《辣椒杂志》 2010年第4期29-32,共4页
摘 要: 以新椒系列辣椒杂交种父母本和一代杂种为材料,采用液氮-SDS法提取辣椒基因组DNA,研究PCR反应的主要影响因子,建立适合辣椒杂交种纯度RAPD分析的PCR反应体系,从120个随机引物中筛选出1个能鉴定新椒10号杂种纯度的引物S1220,从7个随机引物中筛选出1个能鉴定新椒3号杂种纯度的引物S1213。 Some F1 hybrids in Xinjiao hot pepper series and their parents were used as experimental materials in this study.The genomic DNA was extracted with liquid N2-SDS method and the PCR system that was suitable for RAPD analysis of these materials was established.The results showed that primer S1220 could test the purity of F1 hybrid A effectively and S1213 could test the purity of F1 hybrid B effectively.
领 域: [农业科学]