Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

Tyrosinase Polyclonal Antibody, Invitrogen™

Rabbit Polyclonal Antibody

Supplier:  Thermo Scientific PA586261

Catalog No. PIPA586261


Add to Cart

Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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), tyrosinase precursor
Rabbit
Antigen affinity chromatography
RUO
22173, 308800, 7299
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Liquid
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot, Western Blot
1 mg/mL
PBS with 50% glycerol and 0.02% sodium azide, pH 7.2
P11344, P14679
TYR
Synthetic peptide, corresponding to amino acids 470-520 of Human TYR.
100 μL
Primary
Human, Mouse, Rat
Antibody
IgG
Product Suggestions

Product Suggestions

SDS
Documents

Documents

Product Certifications
Promotions

Promotions

Provide Content Correction

We continue to work to improve your shopping experience and your feedback regarding this content is very important to us. Please use the form below to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Cancel Submit