Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

IDS antibody

IDS Reactivity: Human WB, IHC, ELISA, IF Host: Mouse Monoclonal 2D2 unconjugated
Catalog No. ABIN7115175
  • Target See all IDS Antibodies
    IDS (Iduronate 2-Sulfatase (IDS))
    Reactivity
    • 38
    • 7
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    Human
    Host
    • 29
    • 8
    • 3
    Mouse
    Clonality
    • 35
    • 5
    Monoclonal
    Conjugate
    • 25
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IDS antibody is un-conjugated
    Application
    • 39
    • 13
    • 13
    • 13
    • 9
    • 9
    • 4
    • 4
    • 4
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
    Purification
    Protein A+G purification
    Purity
    ≥95 % as determined by SDS-PAGE
    Immunogen
    iduronate 2-sulfatase
    Clone
    2D2
    Isotype
    IgG1
    Top Product
    Discover our top product IDS Primary Antibody
  • Application Notes
    WB: 1:500-1:1000, IHC: 1:20-1:200, IF: 1:20-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide and 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
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    Expiry Date
    12 months
  • Target
    IDS (Iduronate 2-Sulfatase (IDS))
    Alternative Name
    Iduronate 2 sulfatase (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
    Synonyms:IDS, iduronate 2 sulfatase, Idursulfase Background:Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome, an X chromosome-linked disease. IDS is synthesized as two precursor forms of 76 and 90 kDa that are converted, through a 62 kDa intermediate, to 55 and 45 kDa mature polypeptides due to an internal proteolytic cleavage (PMID: 10838181).
    Molecular Weight
    76 kDa, 55 kDa
    Gene ID
    3423
    UniProt
    P22304
    Pathways
    Glycosaminoglycan Metabolic Process
You are here: