用TA法简化入口向量

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}
引用次数: 0

摘要

Gateway技术是一种通用的克隆方法,可以使用λ噬菌体位点特异性重组将DNA片段快速克隆成多个Gateway兼容的目标载体,从而消除了使用限制性内切酶和连接酶的需要。但使用这种系统进行进入克隆的一个问题是昂贵和购买酶的时间长。为了解决这个问题,我们通过对pDONR207进行修饰,创建了每个3 '端包含一个t尾的TA克隆入口载体。TA克隆方法可以简单、经济、快速地构建入口克隆。利用该方法制备的Gateway T载体构建SOS2基因原核表达载体和真核表达载体。通过拟南芥原生质体原核表达和瞬时基因表达的方法,证明SOS2基因在拟南芥原生质体中均有良好的表达
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Simplification of Entry Vector by TA Approach
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
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
New Species of Meconopsis (Papaveraceae) from Laojun Shan and Yao Shan, Northern Yunnan, China Species Diversity and Altitudinal Gradient Patterns of Evergreen Broad-leaved Forest in Meihuashan National Natural Reserve, Fujian Province A Numerical Taxonomic Study of the Euonymus Section Echinococcus ( Celastraceae) A Preliminary Report of Small Mammal Frugivory on Balanophora harlandii (Balanophoraceae) Building a Subtropical Forest Community Phylogeny Based on Plant DNA Barcodes from Dinghushan Plot
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1