RyR-2(Phospho Ser2808) Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in LMNA lead to

Mutations in LMNA lead to several diseases: emery-Dreifuss muscular dystrophy

The encoded protein is a cAMP and cGMP dependent signaling protein and binds to the actin cytoskeleton at extensions of the cell membrane

Defects in this gene are a cause of 3M syndrome type 1 (3M1)

storage and transportation in bioprocessing

This gene encodes a type I transmembrane protein and member of the immunoglobulin superfamily of cell adhesion molecules

RyR-2(Phospho Ser2808) Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in LMNA lead toThis 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.