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Rabbit anti-Human HGD Polyclonal Antibody, FITC conjugated

The antibody against HGD was raised in rabbit using the Recombinant Human Homogentisate 1,2-dioxygenase protein (226-445aa) as the immunogen. This antibody exists as a fitc conjugated isotype IgG, purified by protein G with a purity greater than 95%.

ADC-55092A

The antibody against HGD was raised in rabbit using the Recombinant Human Homogentisate 1,2-dioxygenase protein (226-445aa) as the immunogen. This antibody exists as a fitc conjugated isotype IgG, purified by protein G with a purity greater than 95%.

$299.00

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Specifications


Cat.No ADC-55092A ClonalityPolyclonal
Host SpeciesRabbitTarget NameHGD
Target Synonyms2-dioxygenase (EC 1.13.11.5) (Homogentisate oxygenase) (Homogentisic acid oxidase) (Homogentisicase), HGD, HGO, Homogentisate 1FormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateFITC conjugatedStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Homogentisate 1,2-dioxygenase protein (226-445AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ93099
Background Information
  • Uniprot Id

    Q93099

  • Target Species

    Human

  • Target Name

    HGD

  • Target Full Name

    Homogentisate 1,2-dioxygenase

  • Target Involvement

    Alkaptonuria (AKU)

  • Target Protein Families

    Homogentisate dioxygenase family

  • Target Tissue Specificity

    Highest expression in the prostate, small intestine, colon, kidney and liver.

  • Target Synonyms

    2-dioxygenase; AKU; FLJ94126; hgd; HGD_HUMAN; HGO; Homogentisate 1 2 dioxygenase; Homogentisate 1; Homogentisate oxidase; Homogentisate oxygenase; Homogentisic acid oxidase; Homogentisicase

  • Target 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.

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