Yin Xian-Lun, Wang Chun-tao, Kong Xiang-Xiang, Y. Yongping, Hu Xiangyang
{"title":"用TA法简化入口向量","authors":"Yin Xian-Lun, Wang Chun-tao, Kong Xiang-Xiang, Y. Yongping, Hu Xiangyang","doi":"10.3724/SP.J.1143.2012.11185","DOIUrl":null,"url":null,"abstract":"Gateway technology is a universal cloning approach that enables rapid cloning of DNA fragments into mul- tiple Gateway-compatible destination vectors using λ phage site-specific recombination , eliminating the requirement to work with restriction enzymes and ligase. But a problem using this system for making entry clone is the expensive- ness and long time to buy the enzyme. To solve this problem , we created the TA cloning entry vector that contained a T-tail in each 3 ' -end through modification of pDONR207. The TA cloning approach can construct entry clones simply , economically and rapidly. Using Gateway T vectors prepared by this improved method , prokaryotic expres- sion vector and eukaryotic expression vector for SOS2 gene were constructed. Through the methods of prokaryotic ex- pression and transient gene expression in Arabidopsis protoplasts , it proved that the SOS2 gene expressed well in both","PeriodicalId":20246,"journal":{"name":"Plant Diversity and Resources","volume":"43 1","pages":"397"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simplification of Entry Vector by TA Approach\",\"authors\":\"Yin Xian-Lun, Wang Chun-tao, Kong Xiang-Xiang, Y. Yongping, Hu Xiangyang\",\"doi\":\"10.3724/SP.J.1143.2012.11185\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Gateway technology is a universal cloning approach that enables rapid cloning of DNA fragments into mul- tiple Gateway-compatible destination vectors using λ phage site-specific recombination , eliminating the requirement to work with restriction enzymes and ligase. But a problem using this system for making entry clone is the expensive- ness and long time to buy the enzyme. To solve this problem , we created the TA cloning entry vector that contained a T-tail in each 3 ' -end through modification of pDONR207. The TA cloning approach can construct entry clones simply , economically and rapidly. Using Gateway T vectors prepared by this improved method , prokaryotic expres- sion vector and eukaryotic expression vector for SOS2 gene were constructed. Through the methods of prokaryotic ex- pression and transient gene expression in Arabidopsis protoplasts , it proved that the SOS2 gene expressed well in both\",\"PeriodicalId\":20246,\"journal\":{\"name\":\"Plant Diversity and Resources\",\"volume\":\"43 1\",\"pages\":\"397\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Diversity and Resources\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3724/SP.J.1143.2012.11185\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Diversity and Resources","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3724/SP.J.1143.2012.11185","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Gateway technology is a universal cloning approach that enables rapid cloning of DNA fragments into mul- tiple Gateway-compatible destination vectors using λ phage site-specific recombination , eliminating the requirement to work with restriction enzymes and ligase. But a problem using this system for making entry clone is the expensive- ness and long time to buy the enzyme. To solve this problem , we created the TA cloning entry vector that contained a T-tail in each 3 ' -end through modification of pDONR207. The TA cloning approach can construct entry clones simply , economically and rapidly. Using Gateway T vectors prepared by this improved method , prokaryotic expres- sion vector and eukaryotic expression vector for SOS2 gene were constructed. Through the methods of prokaryotic ex- pression and transient gene expression in Arabidopsis protoplasts , it proved that the SOS2 gene expressed well in both