FA92B Rabbit Polyclonal Antibody, 20ul Cell Separation and Collection Alternative splicing of this gene

Alternative splicing of this gene results in two transcript variants encoding two isoforms differing in only one amino acid

Mutation in this gene results in deletion of the DAG binding-like motif and causes a recessive ataxia

Regulates degradation in lysosomes of a variety of G-protein coupled receptors via its interaction with GPRASP1/GASP1

and is thereby implicated in the development of diabetic complications by catalyzing the reduction of glucose to sorbitol

phosphorylated MBS and consequently inactivated myosin phosphatase

FA92B Rabbit Polyclonal Antibody, 20ul Cell Separation and Collection Alternative splicing of this gene