RyR-2(Phospho Ser2808) Polyclonal Antibody, 20ul Inoculating Loops/Needles Defects in this gene are

Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness

The encoded protein can bind to both B-cell leukemia/lymphoma 3 (BCL-3) and neural precursor cell expressed| developmentally downregulated 4| (Nedd4) proteins

catalyze the conversion of lysophosphatidic acid (LPA) to phosphatidic acid (PA)

Alternative splicing of the C-terminal region of this gene classifies splice variants into two major groups

including suspectibility to diabetes mellitus and systemic juvenile rheumatoid arthritis

RyR-2(Phospho Ser2808) Polyclonal Antibody, 20ul Inoculating Loops/Needles Defects in this gene areThis gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum. The encoded protein is one of the components of a calcium channel, composed of a tetramer of the ryanodine receptor proteins and a tetramer of FK506 binding protein 1B proteins, that supplies calcium to cardiac muscle. Mutations in this gene are associated with stress induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia.