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Tyrosinase Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody
Supplier: Bioss BS0819R

Description
The enzyme encoded by this gene 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.Specifications
Tyrosinase | |
Polyclonal | |
Unconjugated | |
TYR | |
albino; Albino locus protein; ATN; c; CMM8; LB24-AB; Monophenol monooxygenase; Oca1; OCA1A; OCAIA; oculocutaneous albinism IA; SHEP3; SK29-AB; skc35; Tumor rejection antigen AB; TYR; Tyrosinase; tyrosinase (oculocutaneous albinism IA) | |
Rabbit | |
Protein A | |
RUO | |
7299 | |
-20°C | |
Liquid |
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot | |
1 μg/mL | |
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH | |
P14679 | |
TYR | |
KLH conjugated synthetic peptide derived from human Tyrosinase. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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