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MOCOS anticorps

MOCOS Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7257806
  • Antigène Voir toutes MOCOS Anticorps
    MOCOS (Molybdenum Cofactor Sulfurase (MOCOS))
    Reactivité
    • 5
    • 1
    • 1
    Humain
    Hôte
    • 4
    • 1
    Lapin
    Clonalité
    • 4
    • 1
    Polyclonal
    Conjugué
    • 5
    Cet anticorp MOCOS est non-conjugé
    Application
    • 5
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human MOCOS (NP_060417.2).
    Isotype
    IgG
    Top Product
    Discover our top product MOCOS Anticorps primaire
  • Indications d'application
    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
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    MOCOS (Molybdenum Cofactor Sulfurase (MOCOS))
    Autre désignation
    MOCOS (MOCOS Produits)
    Synonymes
    anticorps HMCS, anticorps MCS, anticorps MOS, anticorps 1110018O12Rik, anticorps DDBDRAFT_0217046, anticorps DDBDRAFT_0252757, anticorps DDB_0217046, anticorps DDB_0252757, anticorps Og, anticorps im:7142948, anticorps mocos, anticorps molybdenum cofactor sulfurase, anticorps MOCOS, anticorps Mocos, anticorps AOR_1_1090144, anticorps mocos, anticorps MCYG_05594, anticorps VDBG_04857, anticorps MGYG_02684, anticorps TERG_06775, anticorps mal
    Sujet
    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.
    Poids moléculaire

    Observed_MW: 98 kDa

    Calculated_MW: 98 kDa

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