Literature DB >> 27734387

Design and Analysis of CCN Gene Activity Using CCN Knockout Mice Containing LacZ Reporters.

Jie Jiang1, Zhengshan Hu2, Karen M Lyons3,4.   

Abstract

Two developments have greatly facilitated the construction of CCN mutant mouse strains. The first is the availability of modified embryonic stem (ES) cells and mice developed through several large-scale government-sponsored research programs. The second is the advent of CRISPR/Cas9 technology. In this chapter, we describe the available mouse strains generated by gene targeting techniques and the CCN targeting vectors and genetically modified ES cells that are available for the generation of CCN mutant mice. Many of these mutant mouse lines and ES cells carry a β-galactosidase reporter that can be used to track CCN expression, facilitating phenotypic analysis and revealing new sites of CCN action. Therefore, we also describe a method for β-galactosidase staining.

Entities:  

Keywords:  Cre recombinase; Embryonic stem (ES) cells; Gene targeting; Homologous recombination; International Mouse Phenotyping Consortium (IMPC); LoxP; β-galactosidase

Mesh:

Substances:

Year:  2017        PMID: 27734387     DOI: 10.1007/978-1-4939-6430-7_28

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


  2 in total

1.  Endogenous CCN family member WISP1 inhibits trauma-induced heterotopic ossification.

Authors:  Ginny Ching-Yun Hsu; Simone Marini; Stefano Negri; Yiyun Wang; Jiajia Xu; Chase Pagani; Charles Hwang; David Stepien; Carolyn A Meyers; Sarah Miller; Edward McCarthy; Karen M Lyons; Benjamin Levi; Aaron W James
Journal:  JCI Insight       Date:  2020-07-09

2.  Characterization of bone morphology in CCN5/WISP5 knockout mice.

Authors:  Jie Jiang; Gexin Zhao; Karen M Lyons
Journal:  J Cell Commun Signal       Date:  2018-02-02       Impact factor: 5.908

  2 in total

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