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HGD antibody (AA 374-445)

This Mouse Monoclonal antibody specifically detects HGD in WB, IHC (p) and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7874435
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for HGD antibody (AA 374-445) (ABIN7874435)

Target

See all HGD Antibodies
HGD (Homogentisate 1,2-Dioxygenase (HGD))

Reactivity

  • 49
  • 20
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 60
  • 6
Mouse

Clonality

  • 48
  • 18
Monoclonal

Conjugate

  • 30
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HGD antibody is un-conjugated

Application

  • 50
  • 26
  • 16
  • 16
  • 15
  • 13
  • 13
  • 5
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Clone

2F11E1
  • Binding Specificity

    • 15
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 374-445

    Purpose

    Homogentisate 1,2-dioxygenase Antibody / HGD

    Purification

    Antigen affinity purified

    Immunogen

    Recombinant human protein (amino acids D374-N445) was used as the immunogen for the Homogentisate 1,2-dioxygenase antibody.

    Isotype

    IgG2b
  • Application Notes

    Optimal dilution of the Homogentisate 1,2-dioxygenase antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the Homogentisate 1,2-dioxygenase antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    HGD (Homogentisate 1,2-Dioxygenase (HGD))

    Alternative Name

    Homogentisate 1,2-dioxygenase

    Background

    The HGD gene encodes homogentisate 1,2-dioxygenase (HGD), an enzyme involved in the catabolism of phenylalanine and tyrosine. 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. This gene is mapped to chromosome 3q21-q23 by a preliminary PCR screen of hamster/human somatic cell hybrid genomic DNA samples and by fluorescence in situ hybridization.

    UniProt

    Q93099
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