HGD recombinant monoclonal antibody, clone 20D12

Catalog # RAB07622

Size

Price

Stock

Quantity

Size:100 uL
Price: USD $ 638.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry
Application

Immunohistochemistry

Immunohistochemistry image of HGD recombinant monoclonal antibody, clone 20D12 diluted at 1:100 and staining in paraffin-embedded human liver cancer performed on a Leica BondTM system.

  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against human HGD.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against a synthetic peptide corresponding to human HGD.

    Reactivity

    Human

    Form

    Liquid

    Purification

    Affinity chromatography purification

    Isotype

    IgG

    Recommend Usage

    ELISA
    Immunohistochemistry(1:50-1:200)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In PBS, pH7.4 (150 mM NaCl, 0.02% sodium azide and 50% glycerol)

    Storage Instruction

    Store at -20°C or -80°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Immunohistochemistry

    Immunohistochemistry image of HGD recombinant monoclonal antibody, clone 20D12 diluted at 1:100 and staining in paraffin-embedded human liver cancer performed on a Leica BondTM system.

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — HGD

    Entrez GeneID

    3081

    Protein Accession#

    Q93099

    Gene Name

    HGD

    Gene Alias

    AKU, HGO

    Gene Description

    homogentisate 1,2-dioxygenase (homogentisate oxidase)

    Omim ID

    203500 607474

    Gene Ontology

    Hyperlink

    Gene Summary

    Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26. [provided by RefSeq

    Other Designations

    homogentisate 1,2-dioxygenase|homogentisicase

  • Interactome
  • Pathway
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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