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HGD Rabbit anti-Human, Polyclonal, Bioss

Rabbit Polyclonal Antibody
Supplier: Bioss BS15472R

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.Specifications
HGD | |
Polyclonal | |
Unconjugated | |
HGD | |
Aku; alkaptonuria; HGD; HGO; homogentisate 1, 2-dioxygenase; Homogentisate 1,2-dioxygenase; homogentisate oxidase; Homogentisate oxygenase; Homogentisic acid oxidase; Homogentisicase | |
Rabbit | |
Protein A | |
RUO | |
3081 | |
-20°C | |
Liquid |
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot | |
1 μg/mL | |
PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH | |
Q93099 | |
HGD | |
KLH conjugated synthetic peptide derived from human HGD. | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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