Literature DB >> 29721549

MitoSOX-Based Flow Cytometry for Detecting Mitochondrial ROS.

Megan E Kauffman1, Melinda K Kauffman2, Kassim Traore1, Hong Zhu1, Michael A Trush3, Zhenquan Jia4, Y Robert Li1,4,5,6.   

Abstract

MitoSOX-based assays are widely used to detect mitochondrial reactive oxygen species (ROS), especially superoxide. To this end, 5 μM MitoSOX is commonly used. In this ROS Protocols article, we described the flow cytometric protocol involving the use of various concentrations of MitoSOX (1, 2.5, 5 μM) for detecting mitochondrial ROS in control and mitochondrial DNA-deficient (MD) melanoma B16-F10 cells. We also compared the MitoSOX-based flow cytometry with lucigenin-derived chemiluminometry for their ability to reliably detect the relative differences in mitochondrial ROS formation in the control and MD cells. Our results suggested that 1 μM, rather than the commonly used 5 μM, appeared to be the optimal concentration of MitoSOX for detecting mitochondrial ROS via flow cytometry.

Entities:  

Keywords:  B16-F10 melanoma cells; Chemiluminometry; Flow cytometry; MitoSOX; Mitochondrial DNA-deficient cells; Mitochondrial ROS

Year:  2016        PMID: 29721549      PMCID: PMC5926237          DOI: 10.20455/ros.2016.865

Source DB:  PubMed          Journal:  React Oxyg Species (Apex)


  9 in total

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Review 3.  Hydroethidine- and MitoSOX-derived red fluorescence is not a reliable indicator of intracellular superoxide formation: another inconvenient truth.

Authors:  Jacek Zielonka; B Kalyanaraman
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Journal:  J Biol Chem       Date:  1998-01-23       Impact factor: 5.157

5.  Lucigenin (bis-N-methylacridinium) as a mediator of superoxide anion production.

Authors:  S I Liochev; I Fridovich
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Authors:  Brian A Roelofs; Shealinna X Ge; Paige E Studlack; Brian M Polster
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  9 in total
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