MYL3 Monoclonal Antibody, 100ul[BT-MCA0926] Bio-Reaction Tube osteogenesis imperfecta and Charcot-Marie-Tooth Disease

osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3

tissue specificity:Expressed in all brain regions

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

and activates c-Jun N-terminal kinase (JNK)/stress-activated protein kinase (SAPK) during transient expression in COS and 293 cells

MYL3 Monoclonal Antibody, 100ul[BT-MCA0926] Bio-Reaction Tube osteogenesis imperfecta and Charcot-Marie-Tooth DiseaseMYL3 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.