HGD rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES15769-50, ES15769-100

Citations, Manuals and MSDS Available upon request.

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.[provided by RefSeq, May 2010],

Source: Rabbit

Applications: WB

Dilution: WB 1: 500-2000

Reactivity: Human; Mouse

Immunogen: Synthesized peptide derived from human HGD AA range: 21-71

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 3081

Human SWISS Prot NO: Q93099

Subcellular Location: cytosol, extracellular exosome,

Research Use Only