NCS1 Rabbit Polyclonal Antibody, 20ul Recombinant Protein Defects in MEF2A could be

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

This gene is a member of the melanoma antigen gene (MAGE) family

two pseudogenes

Exchange of hnRNP for mRNA-binding proteins accompanies transport of mRNA from the nucleus to the cytoplasm

NCS1 Rabbit Polyclonal Antibody, 20ul Recombinant Protein Defects in MEF2A could beThis gene is a member of the neuronal calcium sensor gene family which encode calcium binding proteins expressed predominantly in neurons. The protein encoded by this gene regulates G protein coupled receptor phosphorylation in a calcium dependent manner and can substitute for calmodulin. The protein is associated with secretory granules and modulates synaptic transmission and synaptic plasticity. Multiple transcript variants encoding different