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Signal Transduction Metabolism Lipid metabolism

Sphingomyelin Assay Kit (ab133118)

Sphingomyelin Assay Kit (ab133118)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Assay type: Quantitative
  • Detection method: Colorimetric
  • Platform: Microplate reader
  • Sample type: Plasma, Serum

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Overview

  • Product name

    Sphingomyelin Assay Kit
    See all Sphingomyelin kits
  • Detection method

    Colorimetric
  • Precision

    Intra-assay
    Sample n Mean SD CV%
    plasma 16 = 3.9%
    serum 16 = 2.9%
    Inter-assay
    Sample n Mean SD CV%
    plasma 16 = 2.5%
    serum 16 = 2.4%
  • Sample type

    Serum, Plasma
  • Assay type

    Quantitative
  • Range

    5000 µg/dl - 50000 µg/dl
  • Species reactivity

    Reacts with: Mammals, Other species
  • Product overview

    Sphingomyelin Assay Kit (ab133118) provides a specific, sensitive, and convenient method for quantifying sphingomyelin in plasma or serum. In this assay, sphingomyelinase is first used to hydrolyze sphingomyelin to phosphorylcholine and ceramide. Alkaline phosphatase then generates choline from the phosphorylcholine and the newly formed choline is used to generate hydrogen peroxide in a reaction catalyzed by choline oxidase. Finally, with peroxidase as a catalyst, hydrogen peroxide reacts with DAOS and 4-aminoantipyrine to generate a blue color with an optimal absorption at OD595 nm.


    Under the standardized conditions of the assay described in this booklet, the dynamic range of the kit is 5-50 mg/dL sphingomyelin.

  • Notes

    Sphingomyelin (ceramide phosphorylcholine) is an important lipid component of cell membranes and lipoproteins. It consists of a ceramide moiety linked via a phosphodiester bond to phosphorylcholine. Sphingomyelinases are a family of enzymes that can hydrolyze sphingomyelin into ceramide and phosphorylcholine. Ceramides have been implicated as key mediators in signaling pathways, with outcomes as diverse as cell proliferation, differentiation, growth arrest, and apoptosis. An inherited deficiency of acid sphingomyelinase activity results in the sphingomyelin storage disorder Niemann- Pick disease. This disease results in the accumulation of sphinogmyelin in cells, tissues, and fluids. Since sphingomyelin has been implicated in the pathogenesis of several diseases, including atherosclerosis, sensitive and reliable techniques for its quantification are of considerable importance.

    Abcam has not and does not intend to apply for the REACH Authorisation of customers’ uses of products that contain European Authorisation list (Annex XIV) substances.
    It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at +4°C. Please refer to protocols.
  • Components 96 tests
    96-Well Plate (Colorimetric Assay) 1 unit
    96-Well Plate Cover 1 unit
    SM Alkaline Phosphatase 1 vial
    SM Buffer (5X) 1 vial
    SM Color Detector 2 vials
    SM Enzyme Mixture 2 vials
    Sphingomyelin Standard 1 vial
    Sphingomyelinase 1 vial
  • Research areas

    • Kits/ Lysates/ Other
    • Kits
    • Cell Metabolism Kits
    • Lipid Metabolism Kits
    • Lipid metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Lipid and lipoprotein metabolism
    • Lipid metabolism

Images

  • Sphingomyelin standard curve.
    Sphingomyelin standard curve.
    Typical standard curve obtained with sphingomyelin provided following the protocol.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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