HGD rabbit pAb - 50 μL
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. [provided by RefSeq, May 2010],
Distributed by Gentaur
View the Technical Datasheet of the product below
View the Technical Datasheet of the product below