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IDS antibody

IDS Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7259871
  • Target See all IDS Antibodies
    IDS (Iduronate 2-Sulfatase (IDS))
    Reactivity
    • 40
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    Human, Mouse, Rat
    Host
    • 29
    • 10
    • 3
    Rabbit
    Clonality
    • 35
    • 7
    Polyclonal
    Conjugate
    • 27
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IDS antibody is un-conjugated
    Application
    • 41
    • 15
    • 13
    • 13
    • 10
    • 9
    • 6
    • 4
    • 4
    • 4
    • 3
    • 1
    Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human IDS (NP_006114.1).
    Isotype
    IgG
    Top Product
    Discover our top product IDS Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    IDS (Iduronate 2-Sulfatase (IDS))
    Alternative Name
    IDS (IDS Products)
    Synonyms
    mps2 antibody, sids antibody, zgc:158245 antibody, MPS2 antibody, SIDS antibody, AW214631 antibody, iduronate 2-sulfatase antibody, IDS antibody, CpipJ_CPIJ004938 antibody, ids antibody, Ids antibody
    Background
    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.
    Molecular Weight

    Observed_MW: 76 kDa

    Calculated_MW: 34 kDa/38 kDa/61 kDa

    Gene ID
    3423
    UniProt
    P22304
    Pathways
    Glycosaminoglycan Metabolic Process
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