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Lipid Peroxidation (MDA) Assay Kit (Colorimetric) (ab233471)

Price and availability

405 398 ₸

Availability

Order now and get it on Thursday February 25, 2021

Lipid Peroxidation (MDA) Assay Kit (Colorimetric) (ab233471)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Detection method: Colorimetric
  • Platform: Microplate reader

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Overview

  • Product name

    Lipid Peroxidation (MDA) Assay Kit (Colorimetric)
    See all Lipid Peroxidation kits
  • Detection method

    Colorimetric
  • Product overview

    Lipid Peroxidation (MDA) Assay Kit (Colorimetric) ab233471 enables researchers to detect MDA without the heating steps required by the TBARS assay conventionally used for MDA detection.


    In this MDA assay, the MDA Color Reagent reacts with MDA to generate a blue color product which is measured at 695 nm with absorbance microplate readers. The assay is very fast and specific for MDA with little interference from other aldehydes.


    Alternatively, see our popular TBARS assay kit for MDA measurement ab118970.


    MDA assay protocol summary for ab233471:
    - add samples and standards to wells
    - add MDA color reagent and incubate for 10-30 min at room temp
    - add reaction solution and incubate for 30-60 min at room temp
    - analyze with microplate reader 

  • Notes

    Lipid peroxidation is characterized by the oxidative degradation of unsaturated fatty acids, phospholipids, glycolipids, cholesterol esters and cholesterol. Malondialdehyde (MDA) is one of the most commonly used biomarkers for lipid peroxidation.

    Running an MDA assay has historically relied on a reaction with thiobarbituric acid (the TBARS assay) to generate a product that can be measured colorimetrically at 532 nm or fluorimetrically at Ex/Em = 530/550 nm.

    However, the TBARS assay has quite a few limitations:
    - the reaction is not specific to MDA,
    - the TBA-MDA reaction needs be run under acidic conditions,
    - the TBARS assay needs be run under high temperature, commonly at 90-100 ºC.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 200 tests
    Dilution Buffer 1 x 10ml
    MDA Color Reagent 1 vial
    MDA Standard 1 vial
    Reaction Solution 1 x 10ml

Images

  • MDA Standard Curve
    MDA Standard Curve
    MDA Standard Curve

     

  • Signal Comparison of MDA, Formaldehyde, and Glyceraldehyde
    Signal Comparison of MDA, Formaldehyde, and Glyceraldehyde
    Signal Comparison of MDA, Formaldehyde, and Glyceraldehyde

     

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

Alternative products to Lipid Peroxidation (MDA) Assay Kit (Colorimetric) (ab233471)

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    Lipid Peroxidation (MDA) Assay Kit (Colorimetric/Fluorometric) (ab118970)

    Applications:

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    Lipid Peroxidation Assay Kit (Cell-based) (ab243377)

    Applications:

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  • MDA Assay Kit (competitive ELISA) (ab238537)

    Applications:

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