DARPP-32(Phospho Thr75) Polyclonal Antibody, 100ul Vacuum Aspirator CSNB1 is a rare inherited

CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision| myopia| hyperopia| nystagmus and reduced visual acuity

This protein is a member of the ultrahigh sulfur KAP family and the gene is localized to a cluster of KAPs at 17q12-q21

With 250 reactions and a concentration of 1 rxn/μl

STK3 (serine/threonine kinase 3) encodes a serine/threonine protein kinase activated by proapoptotic molecules indicating the encoded protein functions as a growth suppressor

interacts with PtdIns(3

DARPP-32(Phospho Thr75) Polyclonal Antibody, 100ul Vacuum Aspirator CSNB1 is a rare inheritedThis gene encodes a bifunctional signal transduction molecule. Dopaminergic and glutamatergic receptor stimulation regulates its phosphorylation and function as a kinase or phosphatase inhibitor. As a target for dopamine, this gene may serve as a therapeutic target for neurologic and psychiatric disorders. Multiple transcript variants encoding different isoforms have been found for this gene.