TYRP1 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP17543c
Background:
This gene encodes a melanosomal enzyme that belongs to thetyrosinase family and plays an important role in the melaninbiosynthetic pathway. Defects in this gene are the cause of rufousoculocutaneous albinism and oculocutaneous albinism type III.
Other Names:
6-dihydroxyindole-2-carboxylic acid oxidase, DHICA oxidase, 11418-, Catalase B, Glycoprotein 75, Melanoma antigen gp75, Tyrosinase-related protein 1, TRP, TRP-1, TRP1, TYRP1, CAS2, TYRP, TYRRP
Gene Name: TYRP1 (HGNC:12450)
Gene ID: 7306
Primary Accession: P17643
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a melanosomal enzyme that belongs to thetyrosinase family and plays an important role in the melaninbiosynthetic pathway. Defects in this gene are the cause of rufousoculocutaneous albinism and oculocutaneous albinism type III.
Other Names:
6-dihydroxyindole-2-carboxylic acid oxidase, DHICA oxidase, 11418-, Catalase B, Glycoprotein 75, Melanoma antigen gp75, Tyrosinase-related protein 1, TRP, TRP-1, TRP1, TYRP1, CAS2, TYRP, TYRRP
Gene Name: TYRP1 (HGNC:12450)
Gene ID: 7306
Primary Accession: P17643
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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