TRP1 (TYRP1) (NM_000550) Human Recombinant Protein
Product Specifications
Background
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. [provided by RefSeq, Mar 2009]
Synonyms
B-PROTEIN; CAS2; CATB; GP75; OCA3; TRP; TRP1; TYRP
Gene ID
7306
UniProt
P17643
Accession Number mRNA
NM_000550
Chromosomal Location
9p23
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Melanogenesis, Metabolic pathways, Tyrosine metabolism
Field of Research
Melanogenesis, Metabolic pathways, Tyrosine metabolism
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome, Transmembrane
Molecular Weight
58 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
TYRP1
Species
Human
Protein ID
NP_000541
Overview
Recombinant protein of human tyrosinase-related protein 1 (TYRP1)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/7306
Uniprot URL
https://www.uniprot.org/uniprot/P17643
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000550
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000541
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