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AB112134

JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate)

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(2 Reviews)

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(44 Publications)

JC-10 Mitochondrial Membrane Potential Assay Kit ab112134 is designed for use with a microplate reader.
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Functional Studies - JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (AB112134)
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Supplier Data

Functional Studies - JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (AB112134)

JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (ab112134). Camptothecin-induced mitochondria membrane potential changes were measured with JC-10 and JC-1 in Jurkat cells. After Jurkat cells were treated with camptothecin (10 μM) for 4 hours, JC-1 and JC-10 dye loading solutions were added to the wells and incubated for 30 minutes. The fluorescent intensities for both J-aggregates and monomeric forms of JC-1 and JC-10 were measured at Ex/Em = 540/590 nm and 490/525 nm with a microplate reader.

Functional Studies - JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (AB112134)
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PubMed

Functional Studies - JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (AB112134)

Mitochondrial membrane potential measured using ab112134.

CGN were cultured on 96-well white-walled clear-bottom plates in phenol-red free Neurobasal until 7 DIV. Thirty minutes before the end of the treatment, 50 μl of JC-10 dye-loading solution was added to each well and incubated for 30 minutes before measuring fluorescence intensities (Ex/Em  = 485/515 nm and Ex/Em  = 540/590 nm). The change of mitochondrial membrane potential was measured as the ratio between aggregate (Em=590nm) and monomeric forms (Em=515nm) of JC-10. Increasing ratios indicate mitochondrial membrane depolarization.

Kysenius K et al., PLoS One, 9(9). Fig2f. doi: 10.1371/journal.pone.0107129 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

Key facts

Detection method

Fluorescent

Sample types

Suspension cells, Adherent cells

Assay time

1h

Assay Platform

Microplate reader

Product details

JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) ab112134 enables researchers to analyze a JC-10 assay with a microplate reader.

How the assay works
The JC-10 assay provides the most robust assay method for monitoring mitochondria membrane potential changes.

This mitochondrial membrane potential assay protocol is based on the detection of the mitochondrial membrane potential changes in cells by the cationic, lipophilic JC-10 dye. In normal cells, JC-10 concentrates in the mitochondrial matrix where it forms red fluorescent aggregates. However, in apoptotic and necrotic cells, JC-10 diffuses out of mitochondria. It changes to monomeric form and stains cells in green fluorescence.

Although JC-1 is widely used in many labs, its poor water solubility causes great inconvenience. Even at 1 μM concentration, JC-1 tends to precipitate in aqueous buffer. JC-10 is developed to be a superior alternative to JC-1 when high dye concentration is desired. Compared to JC-1, JC-10 has much better water solubility. JC-10 is capable of selectively entering mitochondria, and reversibly changes its color from green to orange as membrane potentials increase. This property is due to the reversible formation of JC-10 aggregates upon membrane polarization that causes shifts in emitted light from 520 nm (i.e. emission of JC-10 monomeric form) to 570 nm (i.e. emission of J-aggregate form). When excited at 490 nm, the color of JC-10 changes reversibly from green to greenish orange as the mitochondrial membrane becomes more polarized.

In normal cells, JC-10 concentrates in the mitochondrial matrix where it forms red fluorescent aggregates. However, in apoptotic and necrotic cells, JC-10 exists in monomeric form and stains cells green. The green emission can be analyzed in fluorescence channel 1 (FL1) and greenish orange emission in channel 2 (FL2). Besides its use in fluorescence microplate platform, it can also be used in fluorescence imaging and flow cytometry.

JC-10 Mitochondrial Membrane Potential Assay Kit protocol summary
- Prepare cells
- Add test compounds
- Add JC-10 dye-working solution (50 μL/well/96-well plate or 12.5 μL/well/384-well plate)
- Incubate at 37°C, 5% CO2 incubator for 30 to 60 minutes
- Add Assay Buffer B (50 μL/well/96-well plate or 12.5 μL/well/384-well plate)
- Monitor fluorescence intensities (bottom read mode) at Ex/Em = 490/525 nm (Cutoff = 515 nm) and 540/590 nm (Cutoff = 570 nm)

How other researchers are using ab112134
JC-10 Mitochondrial Membrane Potential Assay Kit has been used in a variety of sample type including:
- ciPTEC cell lines 1
- HepG2 cells 2
- Ovarian cancer cells 3
References: 1 - Faria j et al. 2023; 2 - Abasi U et al. 2023; 3 - Walker T et al. 2023.

Related and recommended products
If you would like to use JC-10 on a flow cytometer, we recommend ab112133 JC-10 Mitochondrial Membrane Potential Assay Kit (Flow Cytometry)

See other alternative kits to quantify Mitochondrial Membrane Potential:
- JC-1 - Mitochondrial Membrane Potential Assay Kit ab113850
- NIR Mitochondrial Membrane Potential Assay Kit (Flow Cytometry) ab112149
- Orange Mitochondrial Membrane Potential Assay Kit (Flow Cytometry) ab138898
- TMRM Assay Kit (Mitochondrial Membrane Potential) ab228569

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
-20°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The mitochondrial membrane potential also known as Δ ψm is the electrical potential difference across the inner mitochondrial membrane. This potential results from the electrochemical gradient produced by the proton pumps during electron transport chain activity. The mechanical function of the mitochondrial membrane potential is important to ATP production through oxidative phosphorylation. Mitochondrial membranes are widely expressed in almost all eukaryotic cells and are an essential component of cellular metabolism. The inner membrane is structured to facilitate its function housing integral proteins that are key to maintaining the potential.
Biological function summary

The mitochondrial membrane potential drives ATP synthesis by powering ATP synthase an enzyme complex embedded in the mitochondrial membrane. This potential also plays a vital role in other processes such as calcium homeostasis and regulation of mitochondrial biogenesis. The mitochondrial membrane itself forms part of the larger mitochondrial respiratory chain complex coordinating with components like complex I (NADH: ubiquinone oxidoreductase) and complex II (succinate dehydrogenase) to maintain cell energy needs and respond to metabolic demands.

Pathways

The mitochondrial membrane potential is integral to cellular energy metabolism pathways such as the Krebs cycle and oxidative phosphorylation. Mitochondrial membrane potential modulation can affect signaling proteins like cytochrome c which is instrumental in apoptosis. Apoptotic signaling pathways involving proteins such as Bax and Bcl-2 influence the mitochondrial membrane potential and regulate cell survival or death in response to cellular stress or damage.

Changes in the mitochondrial membrane potential relate significantly to conditions like neurodegenerative diseases and cancer. In neurodegenerative diseases such as Parkinson's and Alzheimer's dysregulation of mitochondrial membrane potential can lead to impaired energy production and increased oxidative stress. Cancer cells often exhibit altered mitochondrial membrane potential affecting processes like apoptosis and enabling survival in adverse conditions. These alterations in potential impact proteins such as p53 which play critical roles in cancer progression and neurodegenerative disease pathology.

Product protocols

Target data

Publications (44)

Recent publications for all applications. Explore the full list and refine your search

Endocrinology 166: PubMed39928527

2025

Increased Steroidogenic Acute Regulatory Protein Contributes to Cholesterol-induced β-Cell Dysfunction.

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Species

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Rehana Akter,Meghan F Hogan,Nathalie Esser,Breanne M Barrow,Joseph J Castillo,Edward J Boyko,Andrew T Templin,Rebecca L Hull,Sakeneh Zraika,Steven E Kahn

Nature communications 16:1237 PubMed39890801

2025

PPARα-mediated lipid metabolism reprogramming supports anti-EGFR therapy resistance in head and neck squamous cell carcinoma.

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Valentin Van den Bossche,Julie Vignau,Engy Vigneron,Isabella Rizzi,Hannah Zaryouh,An Wouters,Jérôme Ambroise,Steven Van Laere,Simon Beyaert,Raphaël Helaers,Cédric van Marcke,Lionel Mignion,Elise Y Lepicard,Bénédicte F Jordan,Céline Guilbaud,Olivier Lowyck,Hajar Dahou,Antonella Mendola,Manon Desgres,Léo Aubert,Isabelle Gerin,Guido T Bommer,Romain Boidot,Perrine Vermonden,Aurélien Warnant,Yvan Larondelle,Jean-Pascal Machiels,Olivier Feron,Sandra Schmitz,Cyril Corbet

Cell death discovery 10:514 PubMed39730333

2024

Mitochondria-targeted antioxidant MitoQ radiosensitizes tumors by decreasing mitochondrial oxygen consumption.

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Species

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Justin D Rondeau,Sara Lipari,Barbara Mathieu,Claire Beckers,Justine A Van de Velde,Lionel Mignion,Mauricio Da Silva Morais,Marvin Kreuzer,Ilaria Colauzzi,Tania Capeloa,Martin Pruschy,Bernard Gallez,Pierre Sonveaux

Oncology letters 28:457 PubMed39114572

2024

Metformin in combination with chemotherapy increases apoptosis in gastric cancer cells and counteracts senescence induced by chemotherapy.

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Katia Carolina Vázquez-Ibarra,Josefina Yoaly Sánchez López,Tomás Daniel Pineda Razo,José Roberto Cruz Lozano,Brenda Guadalupe Ortiz-Tamayo,Luis Arturo Palafox-Mariscal,Rosa María González Arreola,Juan Ramón González-García,Pablo Cesar Ortiz-Lazareno

Stem cell research & therapy 14:353 PubMed38072933

2023

Mesenchymal stromal cells secretome restores bioenergetic and redox homeostasis in human proximal tubule cells after ischemic injury.

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Species

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João Faria,Sandra Calcat-I-Cervera,Renata Skovronova,Bonnie C Broeksma,Alinda J Berends,Esther A Zaal,Benedetta Bussolati,Timothy O'Brien,Silvia M Mihăilă,Rosalinde Masereeuw

Scientific reports 13:21915 PubMed38081916

2023

Development of an iron overload HepG2 cell model using ferrous ammonium citrate.

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Species

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Usama Abbasi,Srinivas Abbina,Arshdeep Gill,Jayachandran N Kizhakkedathu

Neuron 111:3988-4005.e11 PubMed37820724

2023

Species-specific FMRP regulation of RACK1 is critical for prenatal cortical development.

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Species

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Minjie Shen,Carissa L Sirois,Yu Guo,Meng Li,Qiping Dong,Natasha M Méndez-Albelo,Yu Gao,Saniya Khullar,Lee Kissel,Soraya O Sandoval,Natalie E Wolkoff,Sabrina X Huang,Zhiyan Xu,Jonathan E Bryan,Amaya M Contractor,Tomer Korabelnikov,Ian A Glass,Dan Doherty,Jon E Levine,André M M Sousa,Qiang Chang,Anita Bhattacharyya,Daifeng Wang,Donna M Werling,Xinyu Zhao

British journal of cancer 128:1765-1776 PubMed36810910

2023

The DNA damage response in advanced ovarian cancer: functional analysis combined with machine learning identifies signatures that correlate with chemotherapy sensitivity and patient outcome.

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Thomas D J Walker,Zahra F Faraahi,Marcus J Price,Amy Hawarden,Caitlin A Waddell,Bryn Russell,Dominique M Jones,Aiste McCormick,N Gavrielides,S Tyagi,Laura C Woodhouse,Bethany Whalley,Connor Roberts,Emma J Crosbie,Richard J Edmondson

Journal of cellular and molecular medicine 26:5728-5741 PubMed36308405

2022

IL-17A promotes lung fibrosis through impairing mitochondrial homeostasis in type II alveolar epithelial cells.

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Species

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Huijuan Xiao,Liang Peng,Dingyuan Jiang,Yuan Liu,Lili Zhu,Zhen Li,Jing Geng,Bingbing Xie,Xiaoxi Huang,Jing Wang,Huaping Dai,Chen Wang

Cancers 14: PubMed36230841

2022

Inhibition of Mitochondrial Redox Signaling with MitoQ Prevents Metastasis of Human Pancreatic Cancer in Mice.

Applications

Unspecified application

Species

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Tania Capeloa,Justine A Van de Velde,Donatienne d'Hose,Sara G Lipari,Françoise Derouane,Loïc Hamelin,Marie Bedin,Thibaut Vazeille,François P Duhoux,Michael P Murphy,Paolo E Porporato,Bernard Gallez,Pierre Sonveaux
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