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  • Iduronate 2 Sulfatase Polyclonal Antibody

    PA5119200

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: PA5119200
      Iduronate 2 Sulfatase Polyclonal Antibody
      Pack Size: 200 μL
      PRICE: 
      CAT NUM: PA5121834
      Iduronate 2 Sulfatase Polyclonal Antibody
      Pack Size: 20 μL
      PRICE: 

      Pack Size
      200 μL, 20 μL
      Storage Temp
      Freezer (-5 to -30 C)
      Brand
      Invitrogen
      Category
      Primary Antibodies
      Antigen
      Iduronate 2 Sulfatase
      Applications
      Western Blot, Immunohistochemistry (Paraffin)
      Classification
      Polyclonal
      Concentration
      0.5 mg/mL
      Conjugate
      Unconjugated
      Form
      Liquid
      Formulation
      PBS with 50% glycerol and 0.05% ProClin 300; pH 7.4
      Gene
      Ids
      Gene Alias
      alpha-L-iduronate sulfate sulfatase; AW214631; Ids; Iduronate 2-sulfatase; iduronate 2-sulfatase (Hunter syndrome); iduronate 2-sulfatase 14 kDa chain
      Gene Accession No
      P22304, Q08890
      Gene ID Entrez
      15931, 3423
      Host Species
      Rabbit
      Immunogen
      Recombinant protein Iduronate-2-Sulfatase. The antigen corresponds to amino acid range 95-289 of the target protein.
      Isotype
      IgG
      Primary or Secondary
      Primary
      Product Type
      Antibody
      Purification Method
      Protein A, Antigen affinity chromatography
      Regulatory Status
      RUO
      Content And Storage
      Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
      Target Species
      Mouse, Human

      Iduronate 2 Sulfatase Polyclonal Antibody for Western Blot, IHC (P) 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 t
      Iduronate 2 Sulfatase Polyclonal Antibody for Western Blot, IHC (P) 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 tRead more ...
      Certifications
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