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This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III.
5,6-dihydroxyindole-2-carboxylic acid oxidase; B; b-PROTEIN; brown; Brown locus protein; CAS2; Catalase B; CATB; DHICA oxidase; glycoprotein 75; GP75; iris stromal atrophy; isa; melanogenic enzyme; melanoma antigen gp75; MGC120175; MGC149362; OCA3; RP11-3L8.1; TRP; TRP1; TRP-1; truncated Tyrp1; TRY1; TRY4; TRYP1; tyrosinase related protein 1; tyrosinase-related protein 1; tyrosinase-related protein 1 precursor; tyrosine phosphatase 1, same as B (Brown); TYRP; Tyrp1; Tyrp-1; TYRRP
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