HGD rabbit pAb

• 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]

• Description :

  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],

• UniProt :

  Q93099

• Swiss Prot :

  Q93099

• Reactivity :

  Human; Mouse

• Immunogen :

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

• Target :

  HGD

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000

• Buffer :

  -20°C/1 year

• Storage Conditions :

  -20°C/1 year

• Fragment :

  IgG

• Subcellular Location :

  Cytosol, extracellular exosome

• Gene ID (Human) :

  3081