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IDS Antikörper

IDS Reaktivität: Human, Maus, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7259871
  • Target Alle IDS Antikörper anzeigen
    IDS (Iduronate 2-Sulfatase (IDS))
    Reaktivität
    • 38
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    Human, Maus, Ratte
    Wirt
    • 28
    • 9
    • 3
    Kaninchen
    Klonalität
    • 34
    • 6
    Polyklonal
    Konjugat
    • 25
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser IDS Antikörper ist unkonjugiert
    Applikation
    • 39
    • 14
    • 13
    • 13
    • 10
    • 9
    • 5
    • 4
    • 4
    • 3
    • 3
    • 1
    Western Blotting (WB)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human IDS (NP_006114.1).
    Isotyp
    IgG
    Top Product
    Discover our top product IDS 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
    IDS (Iduronate 2-Sulfatase (IDS))
    Andere Bezeichnung
    IDS (IDS Produkte)
    Synonyme
    mps2 antikoerper, sids antikoerper, zgc:158245 antikoerper, MPS2 antikoerper, SIDS antikoerper, AW214631 antikoerper, iduronate 2-sulfatase antikoerper, IDS antikoerper, CpipJ_CPIJ004938 antikoerper, ids antikoerper, Ids antikoerper
    Hintergrund
    This gene encodes a member of the sulfatase family of proteins. The encoded preproprotein is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.
    Molekulargewicht

    Observed_MW: 76 kDa

    Calculated_MW: 34 kDa/38 kDa/61 kDa

    Gen-ID
    3423
    UniProt
    P22304
    Pathways
    Glycosaminoglycan Metabolic Process
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