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Cited 9 time in webofscience Cited 9 time in scopus
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dc.contributor.authorDalal, NG-
dc.contributor.authorBentley, WE-
dc.contributor.authorCha, HJ-
dc.date.accessioned2016-04-01T09:13:22Z-
dc.date.available2016-04-01T09:13:22Z-
dc.date.created2009-08-13-
dc.date.issued2005-05-15-
dc.identifier.issn1369-703X-
dc.identifier.other2005-OAK-0000010565-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/29677-
dc.description.abstractA recombinant baculovirus derived from the Autographa californica nuclear polyhedrosis virus (AcNPV) was constructed so that the green fluorescent protein (GFP) was produced via the early-to-late (ETL) promoter. This enabled rapid monitoring of the infection of Sf-9 insect cells. Notably, GFP and its fluorescence appeared similar to 18 h prior to proteins expressed using very late polyhedrin (Polh) promoter. It is anticipated that the use of GFP under the control of ETL promoter will facilitate vector construction, virus isolation, and titer determination. (c) 2005 Elsevier B.V. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE SA-
dc.relation.isPartOfBIOCHEMICAL ENGINEERING JOURNAL-
dc.subjectbaculovirus infection-
dc.subjectearly ETL promoter-
dc.subjectgreen fluorescent protein-
dc.subjectrecombinant protein production-
dc.subjectINSECT-CELL-LINES-
dc.subjectBETA-GALACTOSIDASE-
dc.subjectVECTORS-
dc.subjectLARVAE-
dc.subjectVIRUS-
dc.subjectPURIFICATION-
dc.subjectFUSION-
dc.subjectTITER-
dc.subjectASSAY-
dc.titleFacile monitoring of baculovirus infection for foreign protein expression under very late polyhedrin promoter using green fluorescent protein reporter under early-to-late promoter-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1016/J.BEJ.2005.0-
dc.author.googleDalal, NG-
dc.author.googleBentley, WE-
dc.author.googleCha, HJ-
dc.relation.volume24-
dc.relation.issue1-
dc.relation.startpage27-
dc.relation.lastpage30-
dc.contributor.id10057405-
dc.relation.journalBIOCHEMICAL ENGINEERING JOURNAL-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCHEMICAL ENGINEERING JOURNAL, v.24, no.1, pp.27 - 30-
dc.identifier.wosid000229059600004-
dc.date.tcdate2019-02-01-
dc.citation.endPage30-
dc.citation.number1-
dc.citation.startPage27-
dc.citation.titleBIOCHEMICAL ENGINEERING JOURNAL-
dc.citation.volume24-
dc.contributor.affiliatedAuthorCha, HJ-
dc.identifier.scopusid2-s2.0-17444420288-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc9-
dc.type.docTypeArticle-
dc.subject.keywordPlusINSECT-CELL-LINES-
dc.subject.keywordPlusBETA-GALACTOSIDASE-
dc.subject.keywordPlusVECTORS-
dc.subject.keywordPlusLARVAE-
dc.subject.keywordPlusVIRUS-
dc.subject.keywordPlusPURIFICATION-
dc.subject.keywordPlusFUSION-
dc.subject.keywordPlusTITER-
dc.subject.keywordPlusASSAY-
dc.subject.keywordAuthorbaculovirus infection-
dc.subject.keywordAuthorearly ETL promoter-
dc.subject.keywordAuthorgreen fluorescent protein-
dc.subject.keywordAuthorrecombinant protein production-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaEngineering-

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차형준CHA, HYUNG JOON
Dept. of Chemical Enginrg
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