Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
FIGURE: 1 / 3
Adding 0.2 mL of distilled water will yield a concentration of 500 µg/mL.
This 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Homogentisate 1,2-dioxygenase; homogentisate oxidase; Homogentisate oxygenase; Homogentisic acid oxidase; Homogentisicase
Gene Aliases: AKU; HGD; HGO
UniProt ID: (Human) Q93099
Entrez Gene ID: (Human) 3081
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support