Literature DB >> 19347619

Reporter gene assays.

Andy M F Liu1, David C New, Rico K H Lo, Yung H Wong.   

Abstract

Reporter gene assays are versatile and sensitive methods of assaying numerous targets in high-throughput drug-screening programs. A variety of reporter genes allow users a choice of signal that can be tailored to the required sensitivity, the available detection apparatus, the cellular system employed, and the required compatibility with multiplexed assays. Promoters used to drive reporter gene expression can be activated either by a broad range of biochemical pathways or by the selective activation of individual targets. In this chapter, we will introduce some of the considerations behind the choice of reporter gene assays and describe the methods that we have used to establish 96-well format luciferase and aequorin assays for the screening of ligands for G protein-coupled receptors.

Mesh:

Substances:

Year:  2009        PMID: 19347619     DOI: 10.1007/978-1-60327-545-3_8

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  4 in total

1.  A red fluorescent protein (DsRED) from Discosoma sp. as a reporter for gene expression in walnut somatic embryos.

Authors:  Qixiang Zhang; Sriema L Walawage; David M Tricoli; Abhaya M Dandekar; Charles A Leslie
Journal:  Plant Cell Rep       Date:  2015-01-28       Impact factor: 4.570

Review 2.  Exogenous gene integration mediated by genome editing technologies in zebrafish.

Authors:  Hitoshi Morita; Kiyohito Taimatsu; Kanoko Yanagi; Atsuo Kawahara
Journal:  Bioengineered       Date:  2017-03-08       Impact factor: 3.269

3.  Firefly Luciferase Mutant with Enhanced Activity and Thermostability.

Authors:  Tania Pozzo; Farhima Akter; Yoko Nomura; Angelique Y Louie; Yohei Yokobayashi
Journal:  ACS Omega       Date:  2018-03-06

4.  PlotXpress, a webtool for normalization and visualization of reporter expression data.

Authors:  Elias Brandorff; Marc Galland; Joachim Goedhart
Journal:  F1000Res       Date:  2021-11-08
  4 in total

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