HGD Rabbit Polyclonal Antibody

Ab type

Primary antibody

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.

Reactivity

Human, Mouse

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from human HGD

Storage Stability

-20°C for 1 year

Concentration

1 mg/ml

MolecularWeight_Da

48950

synonyms

HGD