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Signal Transduction Metabolism Mitochondrial

Orange Mitochondrial Membrane Potential Assay Kit (Microplate) (ab138899)

Orange Mitochondrial Membrane Potential Assay Kit (Microplate) (ab138899)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Assay type: Direct
  • Detection method: Fluorescent
  • Platform: Microplate reader
  • Sample type: Adherent cells, Suspension cells

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Overview

  • Product name

    Orange Mitochondrial Membrane Potential Assay Kit (Microplate)
    See all Mitochondrial Membrane Potential kits
  • Detection method

    Fluorescent
  • Sample type

    Adherent cells, Suspension cells
  • Assay type

    Direct
  • Product overview

    Orange Mitochondrial Membrane Potential Assay Kit (Microplate) is designed to detect cell apoptosis by measuring the loss of the mitochondrial membrane potential (MMP). The collapse of mitochondrial membrane potential coincides with the opening of the mitochondrial permeability transition pores, leading to the release of cytochrome C into the cytosol, which in turn triggers other downstream events in the apoptotic cascade.


    ab138899 uses our proprietary cationic MitoOrange Dye for the detection of the mitochondrial membrane potential change in cells. In normal cells, the orange fluorescence intensity is increased when MitoOrange Dye is accumulated in the mitochondria. However, in apoptotic cells, the fluorescence intensity of MitoOrange Dye is decreased following the collapse of MMP. Cells stained with MitoOrange Dye can be fluorometrically monitored at Ex/Em = 540/590 nm. ab138899 provides all the essential components with an optimized assay method. The kit can be used for screening activators and inhibitors of apoptosis. And the assay can be performed in a convenient 96-well and 384-well fluorescence microtiter-plate format without a wash step.

  • Notes

    Related assays

    Review the cell health assay guide to learn about kits to perform a cell viability assay, cytotoxicity assay and cell proliferation assay. 

    Review the metabolism assay guide to learn about assays for metabolites, metabolic enzymes, mitochondrial function, and oxidative stress, and also about how to assay metabolic function in live cells using your plate reader.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 5 x 96 tests
    Assay Buffer A 1 x 50ml
    Assay Buffer B 1 x 25ml
    MitoOrange Dye 1 x 250µl
  • Research areas

    • Cell Biology
    • Apoptosis
    • Mitochondrial
    • Kits/ Lysates/ Other
    • Kits
    • Apoptosis Kits
    • Other Apoptosis Kits
    • Kits/ Lysates/ Other
    • Kits
    • Cell Metabolism Kits
    • Cell Viability and Senescence Kits
    • Kits/ Lysates/ Other
    • Kits
    • Cell Damage Kits
    • Cell viability, plasma membrane damage
    • Metabolism
    • Pathways and Processes
    • Metabolism processes
    • Apoptosis
    • Kits/ Lysates/ Other
    • Kits
    • Cell Damage Kits
    • Cell Damage
    • Kits/ Lysates/ Other
    • Kits
    • Apoptosis Kits
    • Transmembrane potential
    • Cancer
    • Cell Death
    • Apoptosis
    • Mitochondrial
    • Cancer
    • Cell Death
    • Apoptosis
    • Metabolism
    • Metabolism
    • Pathways and Processes
    • Mitochondrial Metabolism
    • Membrane potential
  • Relevance

    Mitochondrial Membrane Potential is an important parameter of mitochondrial function used as an indicator of cell death. The collapse of the mitochondrial Membrane potential coincides with the opening of the mitochondrial permeability transition pores, leading to the release of cytochrome c into the cytosol, which in turn triggers other downstream events in the apoptotic cascade.
  • Alternative names

    • mitochondrial membrane potential

Images

  • Demonstation of decrease in MitoOrange Dye fluorescence with the addition of FCCP in HeLa cells
    Demonstation of decrease in MitoOrange Dye fluorescence with the addition of FCCP in HeLa cells
    The decrease in MitoOrange Dye fluorescence with the addition of FCCP in HeLa cells. HeLa cells were dye loaded with MitoOrange Dye alone or in the presence of 20 µM FCCP for 15 minutes. The fluorescence intensity of MitoOrange Dye was measured 30 minutes after adding Assay Buffer B (Component C) with a microplate reader at Ex/Em = 540/590 nm (cut off 570 nm, bottom read).

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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