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MOCOS Antikörper

MOCOS Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7257806
  • Target Alle MOCOS Antikörper anzeigen
    MOCOS (Molybdenum Cofactor Sulfurase (MOCOS))
    Reaktivität
    • 5
    • 1
    • 1
    Human
    Wirt
    • 4
    • 1
    Kaninchen
    Klonalität
    • 4
    • 1
    Polyklonal
    Konjugat
    • 5
    Dieser MOCOS Antikörper ist unkonjugiert
    Applikation
    • 5
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human MOCOS (NP_060417.2).
    Isotyp
    IgG
    Top Product
    Discover our top product MOCOS Primärantikörper
  • Applikationshinweise
    WB 1:500-1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    MOCOS (Molybdenum Cofactor Sulfurase (MOCOS))
    Andere Bezeichnung
    MOCOS (MOCOS Produkte)
    Synonyme
    HMCS antikoerper, MCS antikoerper, MOS antikoerper, 1110018O12Rik antikoerper, DDBDRAFT_0217046 antikoerper, DDBDRAFT_0252757 antikoerper, DDB_0217046 antikoerper, DDB_0252757 antikoerper, Og antikoerper, im:7142948 antikoerper, mocos antikoerper, molybdenum cofactor sulfurase antikoerper, MOCOS antikoerper, Mocos antikoerper, AOR_1_1090144 antikoerper, mocos antikoerper, MCYG_05594 antikoerper, VDBG_04857 antikoerper, MGYG_02684 antikoerper, TERG_06775 antikoerper, mal antikoerper
    Hintergrund
    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.
    Molekulargewicht

    Observed_MW: 98 kDa

    Calculated_MW: 98 kDa

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