BackgroundThis gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.
DescriptionHGD Recombinant Monoclonal Antibody [20D12]. Unconjugated. Raised in: HEK293F Cell.
FormulationBuffer: Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
SpecificityHuman
IsotypeRabbit IgG
Uniprot IDQ93099
PurificationAffinity Chromatography
ImmunogenA synthesized peptide derived from human HGD
StorageUpon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Alternative NamesHomogentisate 1,2-dioxygenase (EC 1.13.11.5) (Homogentisate oxygenase) (Homogentisic acid oxidase) (Homogentisicase), HGD, HGO
ApplicationELISA, IHC; Recommended dilution: IHC:1:50-1:200
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