CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.

CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.

Science advances (2017-04-26)

Yu Zhang, Chengzu Long, Hui Li, John R McAnally, Kedryn K Baskin, John M Shelton, Rhonda Bassel-Duby, Eric N Olson

ABSTRACT

Duchenne muscular dystrophy (DMD), caused by mutations in the X-linked dystrophin gene (

MATERIALI

N° Catalogo

Marchio

Descrizione del prodotto

Sigma-Aldrich

Anti-vinculina monoclonale, clone hVIN-1, ascites fluid

Sigma-Aldrich

Monoclonal Anti-Dystrophin antibody produced in mouse, clone MANDYS8, ascites fluid