Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/116574
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dc.titleReporter enzyme assays.
dc.contributor.authorPardy, K.
dc.date.accessioned2014-12-12T07:51:32Z
dc.date.available2014-12-12T07:51:32Z
dc.date.issued1993
dc.identifier.citationPardy, K. (1993). Reporter enzyme assays.. Methods in molecular biology (Clifton, N.J.) 18 : 419-424. ScholarBank@NUS Repository.
dc.identifier.issn19406029
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/116574
dc.description.abstractReporter genes code for proteins that have a unique enzymatic activity and are used to assess the transcriptional properties of DNA elements. The use of reporter genes in transgenic animals provides a rapid method for the detection of transgene expression, which is easily distinguishable from expression of the corresponding endogenous gene of the animal. The regulatory sequences of a chosen gene are fused to a readily assayable protein coding region, examples of which are chloramphenicol acetyl transferase (CAT), β-galactosidase, and luciferase. Sensitive assays are available for each of these proteins that facilitate detection and quantitation of transgene expression. The use of these reporter enzymes allows a more rapid and sensitive method of detection than the analysis of specific transgene transcripts within the transgenic animals. The reporter enzymes described in this chapter are CAT, β-galactosidase, and luciferase.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitleMethods in molecular biology (Clifton, N.J.)
dc.description.volume18
dc.description.page419-424
dc.identifier.isiutNOT_IN_WOS
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