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2A - the "go-to" technology for transgene co-expression
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dc.contributor.author | Minskaia, Ekaterina | |
dc.contributor.author | Luke, Garry Alec | |
dc.date.accessioned | 2016-02-03T17:10:05Z | |
dc.date.available | 2016-02-03T17:10:05Z | |
dc.date.issued | 2015-08-26 | |
dc.identifier.citation | Minskaia , E & Luke , G A 2015 , ' 2A - the "go-to" technology for transgene co-expression ' , Single Cell Biology , vol. S1 , no. 004 , pp. 1-3 . https://doi.org/10.4172/2168-9431.S1-004 | en |
dc.identifier.other | PURE: 221892789 | |
dc.identifier.other | PURE UUID: 4deb3847-2e39-4d8a-a243-bae39462efe0 | |
dc.identifier.uri | http://hdl.handle.net/10023/8125 | |
dc.description.abstract | In order to co-express multiple genes for biotechnological and biomedical applications, several approaches have been used with varying degrees of success. Currently, internal ribosome entry site (IRES) elements and “self-cleaving” 2A peptides are the most widely used. The length of the IRES can be prohibitive and IRES-dependent translation of the second open reading frame is often significantly reduced. 2A peptides have gained in popularity due to their small size and ability to consistently produce discrete proteins at an equal level. Here, we promote the use of these sequences as the “go-to” technology for co-expression of multiple proteins. | |
dc.language.iso | eng | |
dc.relation.ispartof | Single Cell Biology | en |
dc.rights | ©2015 Minskaia E, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | en |
dc.subject | Protein co-expression | en |
dc.subject | 2A | en |
dc.subject | Biotechnology | en |
dc.subject | Biomedicine | en |
dc.subject | QH301 Biology | en |
dc.subject | QR Microbiology | en |
dc.subject.lcc | QH301 | en |
dc.subject.lcc | QR | en |
dc.title | 2A - the "go-to" technology for transgene co-expression | en |
dc.type | Journal item | en |
dc.description.version | Publisher PDF | en |
dc.contributor.institution | University of St Andrews. School of Biology | en |
dc.contributor.institution | University of St Andrews. Biomedical Sciences Research Complex | en |
dc.identifier.doi | https://doi.org/10.4172/2168-9431.S1-004 | |
dc.description.status | Peer reviewed | en |
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