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MOCOS antibody

MOCOS Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7257806
  • Target See all MOCOS Antibodies
    MOCOS (Molybdenum Cofactor Sulfurase (MOCOS))
    Reactivity
    • 5
    • 1
    • 1
    Human
    Host
    • 4
    • 1
    Rabbit
    Clonality
    • 4
    • 1
    Polyclonal
    Conjugate
    • 5
    This MOCOS antibody is un-conjugated
    Application
    • 5
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human MOCOS (NP_060417.2).
    Isotype
    IgG
    Top Product
    Discover our top product MOCOS Primary Antibody
  • Application Notes
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MOCOS (Molybdenum Cofactor Sulfurase (MOCOS))
    Alternative Name
    MOCOS (MOCOS Products)
    Synonyms
    HMCS antibody, MCS antibody, MOS antibody, 1110018O12Rik antibody, DDBDRAFT_0217046 antibody, DDBDRAFT_0252757 antibody, DDB_0217046 antibody, DDB_0252757 antibody, Og antibody, im:7142948 antibody, mocos antibody, molybdenum cofactor sulfurase antibody, MOCOS antibody, Mocos antibody, AOR_1_1090144 antibody, mocos antibody, MCYG_05594 antibody, VDBG_04857 antibody, MGYG_02684 antibody, TERG_06775 antibody, mal antibody
    Background
    This gene encodes an enzyme that sulfurates the molybdenum cofactor which is required for activation of the xanthine dehydrogenase (XDH) and aldehyde oxidase (AO) enzymes. XDH catalyzes the conversion of hypoxanthine to uric acid via xanthine, as well as the conversion of allopurinol to oxypurinol, and pyrazinamide to 5-hydroxy pyrazinamide. Mutations in this gene cause the metabolic disorder classical xanthinuria type II which is characterized by the loss of XDH/XO and AO enzyme activity, decreased levels of uric acid in the urine, increased levels of xanthine and hypoxanthine in the serum and urine, formation of xanthine stones in the urinary tract, and myositis due to tissue deposition of xanthine.
    Molecular Weight

    Observed_MW: 98 kDa

    Calculated_MW: 98 kDa

    Gene ID
    55034
    UniProt
    Q96EN8
    Pathways
    Response to Water Deprivation, ER-Nucleus Signaling
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