Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
組織特異性Highest expression in the prostate, small intestine, colon, kidney and liver.
パスウェイAmino-acid degradation; L-phenylalanine degradation; acetoacetate and fumarate from L-phenylalanine: step 4/6.
関連疾患Defects in HGD are the cause of alkaptonuria (AKU) [MIM:203500]. AKU is an autosomal recessive error of metabolism characterized by an increase in the level of homogentisic acid. The clinical manifestations of AKU are urine that turns dark on standing and alkalinization, black ochronotic pigmentation of cartilage and collagenous tissues, and spine arthritis.
配列類似性Belongs to the homogentisate dioxygenase family.