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dc.contributor.author심현보*
dc.date.accessioned2018-11-30T16:30:12Z-
dc.date.available2018-11-30T16:30:12Z-
dc.date.issued2017*
dc.identifier.issn1064-3745*
dc.identifier.otherOAK-23620*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247143-
dc.description.abstractMany large synthetic antibody libraries have been designed, constructed, and successfully generated high-quality antibodies suitable for various demanding applications. While synthetic antibody libraries have many advantages such as optimized framework sequences and a broader sequence landscape than natural antibodies, their sequence diversities typically are generated by random combinatorial synthetic processes which cause the incorporation of many undesired CDR sequences. Here, we describe the construction of a synthetic scFv library using oligonucleotide mixtures that contain predefined, non-combinatorially synthesized CDR sequences. Each CDR is first inserted to a master scFv framework sequence and the resulting single-CDR libraries are subjected to a round of proofread panning. The proofread CDR sequences are assembled to produce the final scFv library with six diversified CDRs. © Springer Science+Business Media LLC 2017.*
dc.description.sponsorshipMinistry of Science ICT and Future Planning*
dc.languageEnglish*
dc.publisherHumana Press Inc.*
dc.subjectAntibody library*
dc.subjectNon-combinatorial CDR diversity*
dc.subjectPhage display*
dc.subjectscFv*
dc.subjectSynthetic antibody library*
dc.subjectSynthetic CDR diversity*
dc.titleConstruction of a scFv library with synthetic, non-combinatorial CDR diversity*
dc.typeBook Chapter*
dc.relation.volume1575*
dc.relation.indexSCOPUS*
dc.relation.startpage15*
dc.relation.lastpage29*
dc.relation.journaltitleMethods in Molecular Biology*
dc.identifier.doi10.1007/978-1-4939-6857-2_2*
dc.identifier.scopusid2-s2.0-85014645387*
dc.author.googleBai X.*
dc.author.googleShim H.*
dc.contributor.scopusid심현보(26635827900)*
dc.date.modifydate20240123110611*
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일반대학원 > 바이오융합과학과 > Journal papers
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