CD58 Polyclonal Antibody, 50ul[BT-AP02487] Cell Senescence Mutations associated with this gene

Mutations associated with this gene cause autosomal recessive spastic paraplegia 13

and is thought to function in a signaling pathway essential for vascular developent

This human protein functions in gliomagenesis and in the suppression of glioma cell growth

This domain is common to a number of hydrolytic enzymes of widely differing phylogenetic origins and catalytic functions

The encoded protein localizes to intracellular membranes

CD58 Polyclonal Antibody, 50ul[BT-AP02487] Cell Senescence Mutations associated with this geneDRD4 encodes the D4 subtype of the dopamine receptor. The D4 subtype is a G protein coupled receptor which inhibits adenylyl cyclase. It is a target for drugs which treat schizophrenia and Parkinson disease. Mutations in DRD4 have been associated with various behavioral phenotypes, including autonomic nervous system dysfunction, attention deficit hyperactivity disorder, and the personality trait of novelty seeking. DRD4 contains a polymorphic number