Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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
100 µL
100 µL
200 µg
100 µL
100 µL
500 µL
100 µL
100 µg
Searching for an antibody we don't offer? We make custom antibodies for specific targets, species and applications.
More than 18,000 custom antibodies created so far.
Talk to a specialist nowIf an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support