TYR Polyclonal Antibody, 20ul Mammalian Expression also known as FG syndrome

also known as FG syndrome

TGFB2 encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins

CLCNKA is a member of the CLC family of voltage-gated chloride channels

The encoded protein may be involved in sensory neuron regulation and in the modulation of pain

This protein is a member of the WD-repeat HIR1 family and may also be involved in DNA repair

TYR Polyclonal Antibody, 20ul Mammalian Expression also known as FG syndromeThe enzyme encoded by TYR catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.