Bio-Connect
WB analysis of human liver lysate using GTX88566 IDS antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human liver lysate using GTX88566 IDS antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human liver lysate using GTX88566 IDS antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer

IDS antibody, Internal

GTX88566
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetIDS
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    IDS antibody, Internal
  • Delivery Days Customer
    7
  • Antibody Specificity
    This antibody is expected to recognize isoform a (NP_000193.1).
  • Application Supplier Note
    WB: 0.1-0.3microg/ml. IHC-P: 3-5microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3423
  • Target name
    IDS
  • Target description
    iduronate 2-sulfatase
  • Target synonyms
    alpha-L-iduronate sulfate sulfatase; ID2S; iduronate 2-sulfatase; iduronate 2-sulfatase 14 kDa chain; iduronate 2-sulfatase 42 kDa chain; idursulfase; MPS2; SIDS
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP22304
  • Protein Name
    Iduronate 2-sulfatase
  • Scientific Description
    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. [provided by RefSeq, Jan 2016]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203