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Invitrogen™ HGD Recombinant Rabbit Monoclonal Antibody (20D12)
Rabbit Recombinant Monoclonal Antibody
Supplier: Invitrogen™ MA550046
Description
HGD Recombinant Monoclonal Antibody for IHC (P), ELISA
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.
Specifications
HGD | |
Recombinant Monoclonal | |
0.4 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
Q93099 | |
HGD | |
A synthesized peptide derived from human HGD. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
ELISA, Immunohistochemistry (Paraffin) | |
20D12 | |
Unconjugated | |
HGD | |
aku; alkaptonuria; HGD; HGO; homogentisate 1, 2-dioxygenase; homogentisate 1,2-dioxygenase; homogentisate oxidase; homogentisate oxygenase; Homogentisic acid oxidase; homogentisicase | |
Rabbit | |
Affinity chromatography | |
RUO | |
3081 | |
-20°C or -80°C if preferred | |
Liquid |
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