MEF-2(Phospho Thr319) Polyclonal Antibody, 20ul Mechanical Pipette Mutations in this gene are

Mutations in this gene are associated with Usher syndrome 2 and familial febrile seizures

|tissue specificity:Highly expressed in macrophage and in monocyte-derived dendritic cells| and thymus

hereditary persistance of alpha-fetoprotein may also be found in individuals with no obvious pathology

MDK has been targeted as a therapeutic for a variety of different disorders

Functions as organic anion exchanger when the uptake of one molecule of organic anion is coupled with an efflux of one molecule of endogenous dicarboxylic acid (glutarate

MEF-2(Phospho Thr319) Polyclonal Antibody, 20ul Mechanical Pipette Mutations in this gene areThe protein encoded by this gene is a DNA binding transcription factor that activates many muscle specific, growth factor induced, and stress induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with