{"title":"夹竹桃科毛蕊花(Plumeria sp.)不同材料DNA产量比较","authors":"Vanesa Vanesa Martida, M. Pharmawati","doi":"10.24843/ATBES.2019.V03.I01.P03","DOIUrl":null,"url":null,"abstract":"DNA extraction that gives good quantity and quality DNA is a basic step that must be completed for molecular studies, especially in DNA fingerprint imaging. The aim of this research was to find out the better quality and quantity of DNA extracted from different plant materials of frangipani cultivars (Plumeria sp.). Leaves and flowers were collected from Taman Jepun, Denpasar Bali. Fresh young leaves and flowers were used as plant materials as well as dried leaves (silica gel dried leaves) of Plumeria sp. This research used CTAB buffer with modification as lysis buffer. Purification techique used NucleoSpin® Gel and PCR Clean Up Kit. The results showed that the colour of DNA solution from fresh material was clear and the quantities of DNA from young fresh leaves were between 70-300 ng/µl. The DNA colour solution from flowers was also transparent with concentration between 0-40 ng/µl. DNA isolated from dry material resulted in brown solution with DNA quantity between 30-100 ng/µl and need to be purified to obtain clear DNA solution.","PeriodicalId":432816,"journal":{"name":"Advances in Tropical Biodiversity and Environmental Sciences","volume":"27 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparison of DNA Yield from Different Plant Materials of Plumeria sp. (Apocynaceae)\",\"authors\":\"Vanesa Vanesa Martida, M. Pharmawati\",\"doi\":\"10.24843/ATBES.2019.V03.I01.P03\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"DNA extraction that gives good quantity and quality DNA is a basic step that must be completed for molecular studies, especially in DNA fingerprint imaging. The aim of this research was to find out the better quality and quantity of DNA extracted from different plant materials of frangipani cultivars (Plumeria sp.). Leaves and flowers were collected from Taman Jepun, Denpasar Bali. Fresh young leaves and flowers were used as plant materials as well as dried leaves (silica gel dried leaves) of Plumeria sp. This research used CTAB buffer with modification as lysis buffer. Purification techique used NucleoSpin® Gel and PCR Clean Up Kit. The results showed that the colour of DNA solution from fresh material was clear and the quantities of DNA from young fresh leaves were between 70-300 ng/µl. The DNA colour solution from flowers was also transparent with concentration between 0-40 ng/µl. DNA isolated from dry material resulted in brown solution with DNA quantity between 30-100 ng/µl and need to be purified to obtain clear DNA solution.\",\"PeriodicalId\":432816,\"journal\":{\"name\":\"Advances in Tropical Biodiversity and Environmental Sciences\",\"volume\":\"27 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in Tropical Biodiversity and Environmental Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.24843/ATBES.2019.V03.I01.P03\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Tropical Biodiversity and Environmental Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24843/ATBES.2019.V03.I01.P03","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
DNA提取是分子研究,特别是DNA指纹成像必须完成的基本步骤。本研究的目的是探讨从鸡蛋花(Plumeria sp.)不同植物材料中提取DNA的最佳质量和数量。叶和花采自巴厘岛登巴萨的塔曼杰潘。以鸡毛花的鲜嫩叶片和花为原料,以干叶(硅胶干叶)为原料,采用改性CTAB缓冲液作为裂解缓冲液。纯化技术采用NucleoSpin®凝胶和PCR Clean Up Kit。结果表明,新鲜材料DNA溶液颜色清晰,鲜叶DNA含量在70 ~ 300 ng/µl之间。从花中提取的DNA显色液也是透明的,浓度在0-40 ng/µl之间。从干燥材料中分离的DNA得到棕色溶液,DNA含量在30-100 ng/µl之间,需要纯化以获得清晰的DNA溶液。
Comparison of DNA Yield from Different Plant Materials of Plumeria sp. (Apocynaceae)
DNA extraction that gives good quantity and quality DNA is a basic step that must be completed for molecular studies, especially in DNA fingerprint imaging. The aim of this research was to find out the better quality and quantity of DNA extracted from different plant materials of frangipani cultivars (Plumeria sp.). Leaves and flowers were collected from Taman Jepun, Denpasar Bali. Fresh young leaves and flowers were used as plant materials as well as dried leaves (silica gel dried leaves) of Plumeria sp. This research used CTAB buffer with modification as lysis buffer. Purification techique used NucleoSpin® Gel and PCR Clean Up Kit. The results showed that the colour of DNA solution from fresh material was clear and the quantities of DNA from young fresh leaves were between 70-300 ng/µl. The DNA colour solution from flowers was also transparent with concentration between 0-40 ng/µl. DNA isolated from dry material resulted in brown solution with DNA quantity between 30-100 ng/µl and need to be purified to obtain clear DNA solution.