Anti-Human/Monkey TYR Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA06079
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the C-terminal region of human TYR
Specificity
Isotype IgG
Reacitivity Human,Monkey
Clone
Uniprot P14679
Concentration 1mg/mL
Dilution WB 1:500-1:2000, ELISA 1:10000
Formulation
Application WB,ELISA
Other Names ATN,CMM8,LB24 AB,LB24-AB,Monophenol monooxygenase,OCA1,OCA1A,OCAIA,Oculocutaneous albinism IA,SHEP3,SK29 AB,SK29-AB,Tumor rejection antigen AB,TYR,TYRO,tyrosinase (oculocutaneous albinism IA),Tyrosinase
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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