首页> 外文期刊>Mitochondrial DNA, Part A >Identification of traditional Chinese medicinal pipefish and exclusion of common adulterants by multiplex PCR based on 12S sequences of specific alleles
【24h】

Identification of traditional Chinese medicinal pipefish and exclusion of common adulterants by multiplex PCR based on 12S sequences of specific alleles

机译:基于12S特异性等位基因的多重PCR鉴定中药液体灭菌和常见掺杂剂排除

获取原文
获取原文并翻译 | 示例
           

摘要

We aimed to establish a rapid and accurate allele-specific diagnostic Polymerase Chain Reaction (PCR) method for medicinal pipefish. To achieve this, pipefish genomic DNA was extracted, sequenced bi-directionally, and the data were analyzed. On this basis, specific identification primers were designed and a facile multiplex PCR system was established and optimized. Phylogenetic tree analysis showed that the six species of pipefish were strictly clustered in separate single branches. The reaction wasoptimized for ease of application, to be used in a reaction volume of 20 uL with template DNA amounts in the range of 5-100ng, and an annealing temperature from 43 to 55 °C. The reactions conducted using authentic samples of Syngnathoides biaculeatus, Solenognathus hardwickii, and Syngnathus acus produced clear single DNA bands of 240 bp, 318 bp, and 139 bp, respectively. The observed amplicons correspond very well to the specific identification primers HLN, HLD, HU, as designed. Thus, it can be concluded that our identification system is specific and stable, and can be used to quickly and accurately identify complex multi-source pipefish samples. We hope that the system will not only ensure the quality of traditional Chinese medicinal ingredients, but also help conservation efforts by offering a quick and easy identification method for pipefish.
机译:我们旨在建立一种快速准确的等位基因特异性诊断聚合酶链反应(PCR)方法,用于药用趋向法。为了实现这一点,提取苯胺基因组DNA,对双向测序,分析数据。在此基础上,设计了特异性鉴定引物,并建立并优化了容易复用PCR系统。系统发育树分析表明,六种产普氏管被严格聚集在单独的单分支中。将反应液化为易于施用,以20μL的反应体积为20μl,模板DNA的量为5-100ng,退火温度为43至55℃。使用Syngnathoides Biacureatus,Solenognathus Hardwickii和Syngnathus ACU的真实样品进行的反应分别产生了240bp,318bp和139bp的清晰单一DNA带。观察到的扩增子对应于特定识别引物HLN,HLD,胡锦涛,如设计。因此,可以得出结论,我们的识别系统是特异性且稳定的,并且可用于快速准确地识别复杂的多源送料样品。我们希望该系统不仅可以确保中药成分的质量,还可以通过为钢丝菲语提供快速简便的识别方法,帮助保护努力。

著录项

  • 来源
    《Mitochondrial DNA, Part A》 |2018年第4期|共7页
  • 作者单位

    School of Traditional Chinese Medicine Capital Medical University Beijing China;

    School of Pharmaceutical Sciences Guizhou University Guiyang China;

    School of Traditional Chinese Medicine Capital Medical University Beijing China;

    State Key Laboratory Breeding Base of Dao-di Herbs National Resource Center for Chinese Materia Medica China Academy of Chinese Medical Sciences Beijing China;

    State Key Laboratory Breeding Base of Dao-di Herbs National Resource Center for Chinese Materia Medica China Academy of Chinese Medical Sciences Beijing China;

    School of Traditional Chinese Medicine Capital Medical University Beijing China;

    School of Traditional Chinese Medicine Capital Medical University Beijing China;

    State Key Laboratory Breeding Base of Dao-di Herbs National Resource Center for Chinese Materia Medica China Academy of Chinese Medical Sciences Beijing China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

    Pipefish; traditional Chinese medicine; molecular discrimination; 12S sequence; multiplex PCR;

    机译:鲍鱼;中药;分子辨别;12s序列;多重PCR;

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