STRUM Rabbit Polyclonal Antibody, 50ul Protein Research This gene encodes a member

This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family

Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses

tissue specificity:Expressed in many tissues

This gene regulates the activation of nuclear receptors

Adenosine monophosphate deaminase 2 encoded by AMPD2 is important in purine metabolism by converting AMP to IMP

STRUM Rabbit Polyclonal Antibody, 50ul Protein Research This gene encodes a memberThis gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin repeat containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive lower