U119A Rabbit Polyclonal Antibody, 100ul Culture Media Required for chromatin and/or kinetochore

Required for chromatin and/or kinetochore dependent microtubule nucleation

Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome

This kinase is activated by various environmental stresses and proinflammatory cytokines

also known as X-linked muscle glycogenosis

U119A Rabbit Polyclonal Antibody, 100ul Culture Media Required for chromatin and/or kinetochoreThis gene is specifically expressed in the photoreceptors in the retina. The encoded product shares strong homology with the C. elegans unc119 protein and it can functionally complement the C. elegans unc119 mutation. It has been localized to the photoreceptor synapses in the outer plexiform layer of the retina and suggested to play a role in the mechanism of photoreceptor neurotransmitter release through the synaptic vesicle cycle. Two transcript