Jie Pan, Rui Feng, Qing Hu, Hong Chen, Su Zhang, Jian Sun, Shen Ji
{"title":"TaqMan实时定量PCR法鉴定中药鹿角。","authors":"Jie Pan, Rui Feng, Qing Hu, Hong Chen, Su Zhang, Jian Sun, Shen Ji","doi":"10.1080/24701394.2020.1741560","DOIUrl":null,"url":null,"abstract":"<p><p>In this study, a method was established for discriminating the true <i>Cervus</i> antlers from its counterfeits using TaqMan real-time quantitative PCR. The method combines the use of true <i>Cervus</i> antlers-specific primers, that amplify a 226 bp fragment from true <i>Cervus</i> antlers DNA, and mammalian-specific primers amplifying a 146 bp fragment from mammalian species DNA, which are used as endogenous control. A TaqMan probe that hybridizes in the '<i>Cervus</i> antler' and also in the 'mammalian' DNA fragments is used to monitor the amplification of the target gene. The <i>Cervus</i> antler mitochondrial DNA was used as target gene to design the primers and TaqMan probes. The data revealed that the TaqMan real-time PCR-based assay can be used for identification of the true <i>Cervus</i> antlers from counterfeits in a single step. The limit of detection (LOD) was lower than 1 pg of DNA per reaction.</p>","PeriodicalId":74204,"journal":{"name":"Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis","volume":"31 5","pages":"173-177"},"PeriodicalIF":0.0000,"publicationDate":"2020-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/24701394.2020.1741560","citationCount":"1","resultStr":"{\"title\":\"TaqMan real-time quantitative PCR for identification of antlers in tradition Chinese medicine.\",\"authors\":\"Jie Pan, Rui Feng, Qing Hu, Hong Chen, Su Zhang, Jian Sun, Shen Ji\",\"doi\":\"10.1080/24701394.2020.1741560\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In this study, a method was established for discriminating the true <i>Cervus</i> antlers from its counterfeits using TaqMan real-time quantitative PCR. The method combines the use of true <i>Cervus</i> antlers-specific primers, that amplify a 226 bp fragment from true <i>Cervus</i> antlers DNA, and mammalian-specific primers amplifying a 146 bp fragment from mammalian species DNA, which are used as endogenous control. A TaqMan probe that hybridizes in the '<i>Cervus</i> antler' and also in the 'mammalian' DNA fragments is used to monitor the amplification of the target gene. The <i>Cervus</i> antler mitochondrial DNA was used as target gene to design the primers and TaqMan probes. The data revealed that the TaqMan real-time PCR-based assay can be used for identification of the true <i>Cervus</i> antlers from counterfeits in a single step. The limit of detection (LOD) was lower than 1 pg of DNA per reaction.</p>\",\"PeriodicalId\":74204,\"journal\":{\"name\":\"Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis\",\"volume\":\"31 5\",\"pages\":\"173-177\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1080/24701394.2020.1741560\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/24701394.2020.1741560\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/5/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/24701394.2020.1741560","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/5/7 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
TaqMan real-time quantitative PCR for identification of antlers in tradition Chinese medicine.
In this study, a method was established for discriminating the true Cervus antlers from its counterfeits using TaqMan real-time quantitative PCR. The method combines the use of true Cervus antlers-specific primers, that amplify a 226 bp fragment from true Cervus antlers DNA, and mammalian-specific primers amplifying a 146 bp fragment from mammalian species DNA, which are used as endogenous control. A TaqMan probe that hybridizes in the 'Cervus antler' and also in the 'mammalian' DNA fragments is used to monitor the amplification of the target gene. The Cervus antler mitochondrial DNA was used as target gene to design the primers and TaqMan probes. The data revealed that the TaqMan real-time PCR-based assay can be used for identification of the true Cervus antlers from counterfeits in a single step. The limit of detection (LOD) was lower than 1 pg of DNA per reaction.