A15587
Size
  • 50ul
  • 100ul
Price
  • $129
  • $229
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Product 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

Source
Rabbit
Applications
WB
Reactivity
Human, Mouse
Dilution
WB 1：500-2000
Storage
-20°C/1 year
Specificity
This antibody detects endogenous levels of HGD at Human/Mouse
Source/Purification
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Immunogen
Synthesized peptide derived from human HGD
Uniprot No
Q93099
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
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
Other
Gene_name: HGD HGO ; Protein_name: HGD; Expression:
Mol.Wt (Da)
49 kD
Concentration
1 mg/ml

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