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IDS anticorps (N-Term)

IDS Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN926632
  • Antigène Voir toutes IDS Anticorps
    IDS (Iduronate 2-Sulfatase (IDS))
    Épitope
    • 15
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reactivité
    • 39
    • 7
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    Humain
    Hôte
    • 29
    • 9
    • 3
    Lapin
    Clonalité
    • 35
    • 6
    Polyclonal
    Conjugué
    • 26
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp IDS est non-conjugé
    Application
    • 40
    • 14
    • 13
    • 13
    • 10
    • 9
    • 5
    • 4
    • 4
    • 3
    • 3
    • 1
    Western Blotting (WB)
    Purification
    Purified
    Immunogène
    IDS antibody was raised in rabbit using the N terminal of IDS as the immunogen
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    Discover our top product IDS Anticorps primaire
  • Indications d'application
    Optimal conditions should be determined by the investigator.
    Commentaires

    IDS Blocking Peptide, catalog no. 33R-8437, is also available for use as a blocking control in assays to test for specificity of this IDS antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    Lot specific
    Buffer
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • 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
    Iduronate-2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked Mucopolysaccharidosis Type II, also known as Hunter Syndrome. Iduronate-2-sulfatase has a strong sequence similarity with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described. Synonyms: Polyclonal IDS antibody, Anti-IDS antibody, iduronate 2-sulfatase antibody, MPS2 antibody, SIDS antibody.
    Pathways
    Glycosaminoglycan Metabolic Process
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