Naylor, Louise H. (1999) Reporter gene technology: The future looks bright. Biochemical Pharmacology, 58 (5). pp. 749-757. ISSN 0006-2952. (doi:10.1016/s0006-2952(99)00096-9) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:16955)
The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. | |
Official URL: https://doi.org/10.1016/s0006-2952(99)00096-9 |
Abstract
Reporter gene technology is widely used to monitor the cellular events associated with signal transduction and gene expression. Based upon the splicing of transcriptional control elements to a variety of reporter genes (with easily measurable phenotypes), it "reports" the effects of a cascade of signalling events on gene expression inside cells. The principal advantage of these assays is their high sensitivity, reliability, convenience, and adaptability to large-scale measurements. This review summarises the current status of reporter gene technology including its role in monitoring gene transfer and expression and its development as a biological screen. With the advances in this technology and in detection methods, it is likely that luciferase and green fluorescent protein will become increasingly popular for the non-invasive monitoring of gene expression in living tissues and cells. Such techniques will be important in defining the molecular events associated with gene transcription, which has implications for our understanding of the molecular basis of disease and will influence our approach to gene therapy and drug development. (C) 1999 Elsevier Science Inc.
Item Type: | Article |
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DOI/Identification number: | 10.1016/s0006-2952(99)00096-9 |
Subjects: | R Medicine > RS Pharmacy and materia medica |
Divisions: | Divisions > Division of Natural Sciences > Biosciences |
Depositing User: | I.T. Ekpo |
Date Deposited: | 30 Mar 2009 18:56 UTC |
Last Modified: | 05 Nov 2024 09:52 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/16955 (The current URI for this page, for reference purposes) |
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