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Article: A recombineering based approach for high-throughput conditional knockout targeting vector construction

TitleA recombineering based approach for high-throughput conditional knockout targeting vector construction
Authors
Issue Date2007
Citation
Nucleic Acids Research, 2007, v. 35, n. 8 How to Cite?
AbstractFunctional analysis of mammalian genes in vivo is primarily achieved through analysing knockout mice. Now that the sequencing of several mammalian genomes has been completed, understanding functions of all the genes represents the next major challenge in the post-genome era. Generation of knockout mutant mice has currently been achieved by many research groups but only by making individual knockouts, one by one. New technological advances and the refinements of existing technologies are critical for genome-wide targeted mutagenesis in the mouse. We describe here new recombineering reagents and protocols that enable recombineering to be carried out in a 96-well format. Consequently, we are able to construct 96 conditional knockout targeting vectors simultaneously. Our new recombineering system makes it a reality to generate large numbers of precisely engineered DNA constructs for functional genomics studies. © 2007 The Author(s).
Persistent Identifierhttp://hdl.handle.net/10722/249016
ISSN
2023 Impact Factor: 16.6
2023 SCImago Journal Rankings: 7.048
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, Waiin-
dc.contributor.authorCostantino, Nina-
dc.contributor.authorLi, Ruixue-
dc.contributor.authorLee, Song Choon-
dc.contributor.authorSu, Qin-
dc.contributor.authorMelvin, David-
dc.contributor.authorCourt, Donald L.-
dc.contributor.authorLiu, Pentao-
dc.date.accessioned2017-10-27T05:58:53Z-
dc.date.available2017-10-27T05:58:53Z-
dc.date.issued2007-
dc.identifier.citationNucleic Acids Research, 2007, v. 35, n. 8-
dc.identifier.issn0305-1048-
dc.identifier.urihttp://hdl.handle.net/10722/249016-
dc.description.abstractFunctional analysis of mammalian genes in vivo is primarily achieved through analysing knockout mice. Now that the sequencing of several mammalian genomes has been completed, understanding functions of all the genes represents the next major challenge in the post-genome era. Generation of knockout mutant mice has currently been achieved by many research groups but only by making individual knockouts, one by one. New technological advances and the refinements of existing technologies are critical for genome-wide targeted mutagenesis in the mouse. We describe here new recombineering reagents and protocols that enable recombineering to be carried out in a 96-well format. Consequently, we are able to construct 96 conditional knockout targeting vectors simultaneously. Our new recombineering system makes it a reality to generate large numbers of precisely engineered DNA constructs for functional genomics studies. © 2007 The Author(s).-
dc.languageeng-
dc.relation.ispartofNucleic Acids Research-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleA recombineering based approach for high-throughput conditional knockout targeting vector construction-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1093/nar/gkm163-
dc.identifier.pmid17426124-
dc.identifier.scopuseid_2-s2.0-34250315750-
dc.identifier.volume35-
dc.identifier.issue8-
dc.identifier.spagenull-
dc.identifier.epagenull-
dc.identifier.eissn1362-4962-
dc.identifier.isiWOS:000247239600042-
dc.identifier.f10001090360-
dc.identifier.issnl0305-1048-

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