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Human ARSB / Arylsulfatase B ELISA Kit (Sandwich ELISA) - LS-F20922

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  • Human ARSB / Arylsulfatase B ELISA Kit (Sandwich ELISA) - LS-F20922
    LS-F20922
    Sandwich ELISA (enzyme-linked immunosorbent assay) kit
    ARSB / Arylsulfatase B
    Human
    This kit recognizes natural and recombinant Human ARSB.
    LS-F20922 is a 96-well enzyme-linked immunosorbent assay (ELISA) for the Quantitative detection of Human ARSB / Arylsulfatase B in samples of Plasma and Serum. It is based upon a Sandwich assay principle and can be used to detect levels of ARSB / Arylsulfatase B as low as 0.156 nanograms per millilter.
     
    Plasma, Serum
    96-Well Microplate
    Colorimetric - 450nm (TMB)
    Quantitative
    0.156 - 10 ng/ml
    0.156 ng/ml
    3.5 h
    Intra-Assay: CV<10% Inter-Assay: CV<10%
    Due to their limited shelf life, LSBio ELISA kits are not typically stocked as finished goods. Upon receipt of an order each kit is assembled and tested to ensure that it meets specifications before shipping. Minor changes may occur to the Range, Sensitivity, and Precision. In the event of a significant change the order would be confirmed with the customer before shipping ELISA kit lot numbers reflect the date of final assembly and testing for each specific kit rather than a bulk manufactured lot. All kits are tested to confirm that they fall within their defined Inter- and Intra- assay coefficient of variation.
    • Coated 96-well Strip Plate
    • Standard (Lyophilized)
    • Sample Diluent
    • Biotinylated Detection Antibody (100x)
    • Biotinylated Detection Antibody Diluent
    • HRP Conjugate (100x)
    • HRP Conjugate Diluent
    • Wash Buffer (25x)
    • TMB Substrate
    • Stop Solution
    • Adhesive Plate Sealers
    Short term: 4°C; Long term: see manual.
    For research use only.
    About ARSB / Arylsulfatase BP15848  NM_000046 NP_000037.2

     ARSB ElisaKit, Arylsulfatase B ElisaKit, ASB ElisaKit, G4S ElisaKit, MPS6 ElisaKit

     Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
    (More About ARSB / Arylsulfatase B)
      

     

     

     

    Sandwich ELISA Platform Overview
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