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

Studies of a similar gene in Drosophila suggested a possible role of this protein in neuronal proliferation and olfactory memory

Rhodopsin kinase phosphorylates rhodopsin and initiates its deactivation

With TC treatment for optimal cell growth

can bypass the interleukin 6 receptor (IL6R) and directly activate this protein

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.