Background:

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.

Classification:

Primary antibody

Alternative names:

HGD

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human HGD

Concentration:

1 mg/ml

Molecular weight:

48950

Applications:

WB

Storage:

-20°C for 1 year

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