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IDS anticorps

IDS Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7259871
  • Antigène Voir toutes IDS Anticorps
    IDS (Iduronate 2-Sulfatase (IDS))
    Reactivité
    • 38
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    Humain, Souris, Rat
    Hôte
    • 28
    • 9
    • 3
    Lapin
    Clonalité
    • 34
    • 6
    Polyclonal
    Conjugué
    • 25
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp IDS est non-conjugé
    Application
    • 39
    • 14
    • 13
    • 13
    • 10
    • 9
    • 5
    • 4
    • 4
    • 3
    • 3
    • 1
    Western Blotting (WB)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human IDS (NP_006114.1).
    Isotype
    IgG
    Top Product
    Discover our top product IDS 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
    IDS (Iduronate 2-Sulfatase (IDS))
    Autre désignation
    IDS (IDS Produits)
    Synonymes
    anticorps mps2, anticorps sids, anticorps zgc:158245, anticorps MPS2, anticorps SIDS, anticorps AW214631, anticorps iduronate 2-sulfatase, anticorps IDS, anticorps CpipJ_CPIJ004938, anticorps ids, anticorps Ids
    Sujet
    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.
    Poids moléculaire

    Observed_MW: 76 kDa

    Calculated_MW: 34 kDa/38 kDa/61 kDa

    ID gène
    3423
    UniProt
    P22304
    Pathways
    Glycosaminoglycan Metabolic Process
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