DUSP19 Polyclonal Antibody, 50ul Mammalian Expression Mutations in this gene can

Mutations in this gene can cause early-onset axonal neuropathy

One of the AUG start codons is polymorphic in human populations

In response to bacterial infection or inflammation

Haploinsufficiency of this gene is implicated in susceptibility to glomerular disease

The encoded protein is localized to the centromere throughout the cell cycle and is required for bipolar spindle assembly

DUSP19 Polyclonal Antibody, 50ul Mammalian Expression Mutations in this gene canDual specificity phosphatases (DUSPs) constitute a large heterogeneous subgroup of the type I cysteine based protein tyrosine phosphatase superfamily. DUSPs are characterized by their ability to dephosphorylate both tyrosine and serine threonine residues. They have been implicated as major modulators of critical signaling pathways. DUSP19 contains a variation of the consensus DUSP C terminal catalytic domain, with the last serine residue replaced by