{"title":"局部热休克的DNA转化","authors":"Sha Li, L. M. Anderson, Liwei Lin, Haw Yang","doi":"10.1109/MEMSYS.2007.4433152","DOIUrl":null,"url":null,"abstract":"DNA transformation by local heat shock using a MEMS device has been successfully demonstrated using an on-chip micro heater and corresponding microfluidic system. The transformation experiments have been conducted and 200% improvement in transformation efficiency was shown as compared with control tests using conventional methodology. Moreover, the green fluorescent proteins expressed from the transformed DNA in cells were verified under a fluorescence microscope, showing all cells grown from antibiotic selection after transformation have transformed DNA working correctly as expected. As such, this work complements other on-going lab-on-a- chip researches for possible gene cloning, gene therapy, and protein expression applications.","PeriodicalId":6388,"journal":{"name":"2007 IEEE 20th International Conference on Micro Electro Mechanical Systems (MEMS)","volume":"36 1","pages":"533-536"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"DNA transformation by local heat shock\",\"authors\":\"Sha Li, L. M. Anderson, Liwei Lin, Haw Yang\",\"doi\":\"10.1109/MEMSYS.2007.4433152\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"DNA transformation by local heat shock using a MEMS device has been successfully demonstrated using an on-chip micro heater and corresponding microfluidic system. The transformation experiments have been conducted and 200% improvement in transformation efficiency was shown as compared with control tests using conventional methodology. Moreover, the green fluorescent proteins expressed from the transformed DNA in cells were verified under a fluorescence microscope, showing all cells grown from antibiotic selection after transformation have transformed DNA working correctly as expected. As such, this work complements other on-going lab-on-a- chip researches for possible gene cloning, gene therapy, and protein expression applications.\",\"PeriodicalId\":6388,\"journal\":{\"name\":\"2007 IEEE 20th International Conference on Micro Electro Mechanical Systems (MEMS)\",\"volume\":\"36 1\",\"pages\":\"533-536\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2007 IEEE 20th International Conference on Micro Electro Mechanical Systems (MEMS)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/MEMSYS.2007.4433152\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2007 IEEE 20th International Conference on Micro Electro Mechanical Systems (MEMS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MEMSYS.2007.4433152","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
DNA transformation by local heat shock using a MEMS device has been successfully demonstrated using an on-chip micro heater and corresponding microfluidic system. The transformation experiments have been conducted and 200% improvement in transformation efficiency was shown as compared with control tests using conventional methodology. Moreover, the green fluorescent proteins expressed from the transformed DNA in cells were verified under a fluorescence microscope, showing all cells grown from antibiotic selection after transformation have transformed DNA working correctly as expected. As such, this work complements other on-going lab-on-a- chip researches for possible gene cloning, gene therapy, and protein expression applications.