{"title":"互补脱氧核糖核酸减法。","authors":"E. Hara, K. Oda","doi":"10.32388/qapjdo","DOIUrl":null,"url":null,"abstract":"A difference cloning method and a technique for comparison of two closely related cell types, e.g. a differentiated or transformed cell (tester) and the undifferentiated or normal cell (driver). Driver RNA is converted to double-strand cDNA, usually with the incorporation of a tagged nucleotide, while the tester RNA is converted to first-strand cDNA (with no tag). T he two preparations are mixed, melted and annealed to form, among other species, heteroduplexes composed of one strand from each of the different sources. T he annealed heteroduplexes, as well as other driver species are captured by the tagged nucleotide and removed from the mixture. T he resulting pool will be enriched for those cDNA species unique to the tester cells. Following second-strand synthesis, the double-stranded cDNAs are cloned. T he resulting cDNA library will be enriched for sequences expressed only in the tester cells. cDNA subtraction can also be done by PCR. (NCI/OSP) Qeios · Definition, February 2, 2020","PeriodicalId":22197,"journal":{"name":"Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme","volume":"43 1","pages":"482-8"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[cDNA subtraction].\",\"authors\":\"E. Hara, K. Oda\",\"doi\":\"10.32388/qapjdo\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A difference cloning method and a technique for comparison of two closely related cell types, e.g. a differentiated or transformed cell (tester) and the undifferentiated or normal cell (driver). Driver RNA is converted to double-strand cDNA, usually with the incorporation of a tagged nucleotide, while the tester RNA is converted to first-strand cDNA (with no tag). T he two preparations are mixed, melted and annealed to form, among other species, heteroduplexes composed of one strand from each of the different sources. T he annealed heteroduplexes, as well as other driver species are captured by the tagged nucleotide and removed from the mixture. T he resulting pool will be enriched for those cDNA species unique to the tester cells. Following second-strand synthesis, the double-stranded cDNAs are cloned. T he resulting cDNA library will be enriched for sequences expressed only in the tester cells. cDNA subtraction can also be done by PCR. (NCI/OSP) Qeios · Definition, February 2, 2020\",\"PeriodicalId\":22197,\"journal\":{\"name\":\"Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme\",\"volume\":\"43 1\",\"pages\":\"482-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32388/qapjdo\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/qapjdo","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A difference cloning method and a technique for comparison of two closely related cell types, e.g. a differentiated or transformed cell (tester) and the undifferentiated or normal cell (driver). Driver RNA is converted to double-strand cDNA, usually with the incorporation of a tagged nucleotide, while the tester RNA is converted to first-strand cDNA (with no tag). T he two preparations are mixed, melted and annealed to form, among other species, heteroduplexes composed of one strand from each of the different sources. T he annealed heteroduplexes, as well as other driver species are captured by the tagged nucleotide and removed from the mixture. T he resulting pool will be enriched for those cDNA species unique to the tester cells. Following second-strand synthesis, the double-stranded cDNAs are cloned. T he resulting cDNA library will be enriched for sequences expressed only in the tester cells. cDNA subtraction can also be done by PCR. (NCI/OSP) Qeios · Definition, February 2, 2020