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dc.contributor.authorBeer, Ralf
dc.contributor.authorChristiansen, Tania
dc.contributor.authorHerbst, Konrad
dc.contributor.authorIgnatiadis, Nikolaos
dc.contributor.authorKats, Ilia
dc.contributor.authorKurzawa, Nils
dc.contributor.authorMeichsner, Johanna
dc.contributor.authorRabe, Sophie
dc.contributor.authorRiedel, Anja
dc.contributor.authorSachs, Joshua
dc.contributor.authorSchessner, Julia
dc.contributor.authorSchmidt, Florian
dc.contributor.authorWalch, Philipp
dc.contributor.authorAdlung, Lorenz
dc.contributor.authorGenereith, Katharina
dc.contributor.authorGeorgi, Fanny
dc.contributor.authorHeinemann, Tim
dc.contributor.authorMeyer, Hannah
dc.contributor.authorNiopek, Dominik
dc.contributor.authorDi Ventura, Barbara
dc.contributor.authorEils, Roland
dc.date.accessioned2013-10-05T00:50:45Z
dc.date.available2013-10-05T00:50:45Z
dc.date.issued2013-10-04
dc.identifier.urihttp://hdl.handle.net/1721.1/81332
dc.description.abstractThe purpose of this RFC is to provide instructions for a rapid and cost efficient cloning and transformation method which allows for the manufacturing of multi-fragment plasmid constructs in a parallelized manner: High Throughput Circular Extension Cloning and Transformation (HiCT). Description of construct libraries generated by the HiCT method can be found at http://2013.igem.org/Team:Heidelberg/Indigoidine. This RFC also points out further optimization strategies with regard to construct stability, reduction of transformation background and the generation of competent cells.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesBBF RFC;99
dc.rightsAttribution-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nd/3.0/us/*
dc.subjectDNA assemblyen_US
dc.titleHiCT: High Throughput Protocols For CPE Cloning And Transformationen_US
dc.typeTechnical Reporten_US


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