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dc.creatorSong,Ping
dc.creatorWang,Hwa-Chain Robert
dc.date2004-08-01
dc.date.accessioned2019-11-14T12:58:51Z
dc.date.available2019-11-14T12:58:51Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-34582004000200013
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/119137
dc.descriptionThe technology of tetracycline-inducible gene expression has been successfully used in experimental biology to identify the function and downstream signaling pathways of an interested gene. It has been significantly improved to meet the criteria with specificity to exogenous non-toxic inducers, independent regulation from cellular pathways, and dose-dependent inducibility and reversibility. However, to establish tetracycline-inducible gene expression in mammalian cells is still a time-and effort-consuming process. With a tetracycline-inducible gene expression system T-REx, we have developed a practical protocol to use the oncogenic H-ras gene as a dominant reporter gene to increase efficiency in attaining desired cell lines in which ectopic expression of a particular gene in cells can be introduced and reversibly induced by the presence or absence of tetracycline in cultures.
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dc.languageen
dc.publisherPontificia Universidad Católica de Valparaíso
dc.relation10.4067/S0717-34582004000200013
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceElectronic Journal of Biotechnology v.7 n.2 2004
dc.titleEfficient identification of tetR-expressing cell lines for tetracycline-regulated gene expression


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