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Rabbit anti-Human HGD Polyclonal Antibody

The antibody against HGD was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 226-445 of human HGD (NP_000178.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-02926A

The antibody against HGD was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 226-445 of human HGD (NP_000178.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-02926A ClonalityPolyclonal
Host SpeciesRabbitTarget NameHGD
Target SynonymsAKU; HGO; HGDFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesSKOV3ApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 226-445 of human HGD (NP_000178.2).Target SpeciesHuman
Uniprot IDQ93099Immunogen Sequence
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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