DC Field | Value | Language |
---|---|---|
dc.contributor.author | 강창원 | ko |
dc.contributor.author | 남상철 | ko |
dc.date.accessioned | 2013-02-27T08:10:52Z | - |
dc.date.available | 2013-02-27T08:10:52Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1988 | - |
dc.identifier.citation | KOREAN BIOCHEMICAL JOURNAL, v.21, no.3, pp.306 - 311 | - |
dc.identifier.issn | 0368-4881 | - |
dc.identifier.uri | http://hdl.handle.net/10203/67403 | - |
dc.description.abstract | In the in vitro transcription reactions limiting concentrations of a ribonucleotide cause the phage SP6 RNA polymerase to pause long enough specifically only at the positions of the limited nucleotide and dissociate from the elongation complex. As a result a series of RNA oligomers comprising a sequencing ladder was obtained in high-resolution polyacrylamide-urea gel electrophoresis. Also, RNA oligomers up to 6-mer were made not only nucleotide-specifically, but also non-specifically. According to these results, the phage SP6 RNA polymerase appears to escape from the abortive initiation cycling after synthesizing 6 base long RNA, then get into the stable elongation mode as 7 base long RNA is made. | - |
dc.language | Korean | - |
dc.publisher | 생화학분자생물학회 | - |
dc.title | 파아지 SP6 RNA 중합효소에 의한 전사의 연속성 | - |
dc.title.alternative | Processivity of Phage SP6 RNA Polymerase transcription | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.citation.volume | 21 | - |
dc.citation.issue | 3 | - |
dc.citation.beginningpage | 306 | - |
dc.citation.endingpage | 311 | - |
dc.citation.publicationname | KOREAN BIOCHEMICAL JOURNAL | - |
dc.contributor.localauthor | 강창원 | - |
dc.contributor.nonIdAuthor | 남상철 | - |
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