ARHG4 Polyclonal Antibody, 20ul ssDNA Synthesis CSNB1 is a rare inherited

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

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

They are found to bind common hematopoietin receptor subunits

which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development

ARHG4 Polyclonal Antibody, 20ul ssDNA Synthesis CSNB1 is a rare inheritedRho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The protein encoded by this gene may form complex with G proteins and stimulate Rho dependent signals. Multiple alternatively spliced transcript variants encoding different isoforms have been found, but the full length nature of some variants has not been determined.