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XDH antibody

This anti-XDH antibody is a Rabbit Monoclonal antibody detecting XDH in WB and IHC (p). Suitable for Human, Mouse and Rat.
Catalog No. ABIN6945395

Quick Overview for XDH antibody (ABIN6945395)

Target

See all XDH Antibodies
XDH (Xanthine Dehydrogenase (XDH))

Reactivity

  • 45
  • 24
  • 17
  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 54
  • 12
  • 1
Rabbit

Clonality

  • 44
  • 23
Monoclonal

Conjugate

  • 35
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
This XDH antibody is un-conjugated

Application

  • 45
  • 31
  • 20
  • 19
  • 12
  • 10
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

2D9
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    Recombinant protein within human Xanthine Oxidase aa 100-300.

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC-P 1:200-400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 1xTBS ( pH 7.4), 1 % BSA, 40 %Glycerol and 0.05 % Sodium Azide.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C for 12 months.

    Expiry Date

    12 months
  • Target

    XDH (Xanthine Dehydrogenase (XDH))

    Alternative Name

    Xanthine Oxidase

    Background

    Synonyms: Xanthine dehydrogenase/oxidase, Xanthine dehydrogenase, Xanthine oxidase, Xanthine oxidoreductase, XD, XO, XOR, XDH, XDHA

    Background: The process of metabolizing purines to a common molecule known as xanthine is an essential process for the proper shuttling of uric acid. Xanthine oxidase is a flavoprotein enzyme that coordinates molybdenum and utilizes NAD+ as an electron acceptor to catalyze the oxidation of hypoxanthine to xanthine and then to uric acid. The predominant form of this enzyme is xanthine dehydrogenase, which is a homodimer that can be converted to xanthine oxidase by sulfhydryl oxidation or proteolytic modification. Xanthine oxidase is present in species ranging from bacteria to human and is ubiquitously expressed in mammalian tissues. In the oxidase form, this enzyme is coupled to the generation of free radicals. Individuals showing marked elevation of serum xanthine oxidase is suggestive of chronic liver disease and cholestasis, which is a condition defined by hepatic obstruction. Hepatic obstruction causes bile salts, the bile pigment bilirubin, and fats to accumulate in the blood stream instead of being eliminated normally. The clinical consequences of defects in xanthine oxidase range from mild to severe and even contribute to fatal disorders.

    Gene ID

    7498

    UniProt

    P47989

    Pathways

    Positive Regulation of Endopeptidase Activity
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