SNTA1 Rabbit Polyclonal Antibody, 50ul Immuno Plates Mutations in this gene cause

Mutations in this gene cause atrial septal defect with atrioventricular conduction defect

and is associated with several disease states including cancer and Alzheimer's disease

online information:GlycoGene database

and may also regulate the cystic fibrosis transmembrane regulator(CFTR) ion channel

SNTA1 Rabbit Polyclonal Antibody, 50ul Immuno Plates Mutations in this gene causeSyntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N terminal PDZ domain of this syntrophin protein interacts with the C terminus of the pore forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1. 5. This protein also associates