首页> 外文期刊>Journal of Korean Forestry Society >Detection method of Genetic Variation of Mulberry Dwarf Phytoplasma by PCR-SSCP Analysis
【24h】

Detection method of Genetic Variation of Mulberry Dwarf Phytoplasma by PCR-SSCP Analysis

机译:PCR-SSCP分析检测桑树矮小植原体遗传变异的方法

获取原文
获取原文并翻译 | 示例
           

摘要

Single-strand conformation polymorphism (SSCP) analysis of MD and JWB phytopalsma isolates which amplified PCR products using the R16F2n/R2 phytoplamsa universal primer pair were compared for variations of their nucleotide sequence. The MD and JWB phytoplasmas were clearly distinct each of the band patterns from about 1.2kb PCR products. To clearly distinct of close SSCP band patterns, the MD and JWB phytoplasma PCR products were mixed and performed to detect their polymorphism. The SSCP band patterns show all of bands of MD and JWB on single lane and easily distinct their each band patterns. The PCR-SSCP analysis was possible to detect of 1.2kb nucleotide sequence and near close band patterns were easily distinct by mixing two samples.
机译:比较了使用R16F2n / R2 phylamlamsa通用引物对扩增了PCR产物的MD和JWB phytopalsma分离株的单链构象多态性(SSCP),分析了其核苷酸序列的变异。 MD和JWB的植物原质明显区别于约1.2kb PCR产物的每个条带模式。为了清楚地区分接近的SSCP带模式,将MD和JWB植物质浆PCR产物混合并进行检测以检测它们的多态性。 SSCP频段模式显示了单通道MD和JWB的所有频段,并轻松区分它们的每个频段模式。 PCR-SSCP分析可以检测到1.2kb的核苷酸序列,并且通过混合两个样品可以很容易地区分出接近的近带模式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号