MYL3 Monoclonal Antibody, 100ul[BT-MCA0926] Bio-Reaction Tube tissue specificity:Expressed in all brain

tissue specificity:Expressed in all brain regions

Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia

Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects

mitochondrial Fo complex subunit C2) encodes a subunit of mitochondrial ATP synthase

The encoded enzyme participates in the DNA repair pathway by initiating base excision repair by removing damaged bases

MYL3 Monoclonal Antibody, 100ul[BT-MCA0926] Bio-Reaction Tube tissue specificity:Expressed in all brainMYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid left ventricular chamber type hypertrophic cardiomyopathy.