Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/116574
Title: Reporter enzyme assays.
Authors: Pardy, K. 
Issue Date: 1993
Citation: Pardy, K. (1993). Reporter enzyme assays.. Methods in molecular biology (Clifton, N.J.) 18 : 419-424. ScholarBank@NUS Repository.
Abstract: Reporter 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.
Source Title: Methods in molecular biology (Clifton, N.J.)
URI: http://scholarbank.nus.edu.sg/handle/10635/116574
ISSN: 19406029
Appears in Collections:Staff Publications

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