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dc.contributor.authorHaddock, Traci L.
dc.contributor.authorDensmore, Douglas M.
dc.contributor.authorAppleton, Evan
dc.contributor.authorCarr, Swati
dc.contributor.authorIverson, Sonya
dc.contributor.authorDe Freitas, Monique
dc.contributor.authorJin, Shawn
dc.contributor.authorAwtry, Jake
dc.contributor.authorDesai, Devina
dc.contributor.authorLozanoski, Thomas
dc.contributor.authorShah, Pooja
dc.contributor.authorAgarwal, Yash
dc.contributor.authorLewis, Kathleen
dc.contributor.authorPacheco, Alan
dc.date.accessioned2015-08-29T02:22:56Z
dc.date.available2015-08-29T02:22:56Z
dc.date.issued2015-08-28
dc.identifier.urihttp://hdl.handle.net/1721.1/98267
dc.description.abstractThis RFC94 describes an assembly standard based on the Type IIS restriction enzymes BsaI and BbsI (also called BpiI). This assembly standard is based upon the Modular Cloning (MoClo) assembly strategy, which was introduced in 2011 by Weber et al. [1] and is based upon Golden Gate cloning [2]. In this RFC, we describe our proposed MoClo standard for generating a library of bacterial DNA parts for generating four-part transcriptional units (promoter : 5’UTR : CDS : 3’UTR). In this work, we define 5’UTRs as including ribosomal binding sites (RBS) and bi-cistronic design elements (BCDs) [3], and 3’UTRs as transcriptional terminators. The 2012-2014 BostonU iGEM teams completed this work and a more compact library has also been created based on this work [4].en_US
dc.language.isoen_USen_US
dc.relation.ispartofseriesBBF RFC;94
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectassembly standarden_US
dc.titleBBF RFC 94: Type IIS Assembly for Bacterial Transcriptional Units: A Standardized Assembly Method for Building Bacterial Transcriptional Units Using the Type IIS Restriction Enzymes BsaI and BbsIen_US
dc.typeTechnical Reporten_US


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