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AB112134

JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate)

5

(2 Reviews)

|

(39 Publications)

JC-10 Mitochondrial Membrane Potential Assay Kit ab112134 is designed for use with a microplate reader.
2 Images
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)
  • FuncS

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?

{ "values": { "5x96Tests": { "sellingSize": "5 x 96 Tests", "publicAssetCode":"ab112134-5x96Tests", "assetComponentDetails": [ { "size":"1 x 25 mL", "name":"Assay Buffer B", "number":"AB112134-CMP03", "productcode":"" }, { "size":"1 x 25 mL", "name":"Assay Buffer A", "number":"AB112134-CMP02", "productcode":"" }, { "size":"1 x 250 µL", "name":"100X JC-10 in DMSO", "number":"AB112134-CMP01", "productcode":"" } ] } } }

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

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Publications (39)

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

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.

Applications

Unspecified application

Species

Unspecified reactive species

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.

Applications

Unspecified application

Species

Unspecified reactive species

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

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.

Applications

Unspecified application

Species

Unspecified reactive species

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.

Applications

Unspecified application

Species

Unspecified reactive species

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

Unspecified reactive species

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

Frontiers in immunology 13:918551 PubMed36248901

2022

Complement membrane attack complex is an immunometabolic regulator of NLRP3 activation and IL-18 secretion in human macrophages.

Applications

Unspecified application

Species

Unspecified reactive species

Gisela Jimenez-Duran,Joseph Kozole,Rachel Peltier-Heap,Eleanor R Dickinson,Christopher R Kwiatkowski,Francesca Zappacosta,Roland S Annan,Nicholas W Galwey,Eva-Maria Nichols,Louise K Modis,Martha Triantafilou,Kathy Triantafilou,Lee M Booty

Nature communications 13:4142 PubMed35842441

2022

ZnT8 loss-of-function accelerates functional maturation of hESC-derived β cells and resists metabolic stress in diabetes.

Applications

Unspecified application

Species

Unspecified reactive species

Qing Ma,Yini Xiao,Wenjun Xu,Menghan Wang,Sheng Li,Zhihao Yang,Minglu Xu,Tengjiao Zhang,Zhen-Ning Zhang,Rui Hu,Qiang Su,Fei Yuan,Tinghui Xiao,Xuan Wang,Qing He,Jiaxu Zhao,Zheng-Jun Chen,Zhejin Sheng,Mengyao Chai,Hong Wang,Weiyang Shi,Qiaolin Deng,Xin Cheng,Weida Li

Frontiers in aging neuroscience 14:869558 PubMed35721026

2022

Growth Differentiation Factor 15 Protects SH-SY5Y Cells From Rotenone-Induced Toxicity by Suppressing Mitochondrial Apoptosis.

Applications

Unspecified application

Species

Unspecified reactive species

Peizheng Li,Hongbo Lv,Bohan Zhang,Ruonan Duan,Xiufang Zhang,Pengfei Lin,Chengyuan Song,Yiming Liu

Frontiers in physiology 13:772313 PubMed35464086

2022

A Synthetic Small RNA Homologous to the D-Loop Transcript of mtDNA Enhances Mitochondrial Bioenergetics.

Applications

Unspecified application

Species

Unspecified reactive species

Theodore L Mathuram,Danyelle M Townsend,Vincent J Lynch,Ilya Bederman,Zhi-Wei Ye,Jie Zhang,Wade J Sigurdson,Erin Prendergast,Raul Jobava,Jonathan P Ferruzza,Mary R D'Angelo,Maria Hatzoglou,Yaron Perry,Anna Blumental-Perry

Cancers 14: PubMed35326667

2022

MitoQ Inhibits Human Breast Cancer Cell Migration, Invasion and Clonogenicity.

Applications

Unspecified application

Species

Unspecified reactive species

Tania Capeloa,Joanna Krzystyniak,Donatienne d'Hose,Amanda Canas Rodriguez,Valery L Payen,Luca X Zampieri,Justine A Van de Velde,Zohra Benyahia,Erica Pranzini,Thibaut Vazeille,Maude Fransolet,Caroline Bouzin,Davide Brusa,Carine Michiels,Bernard Gallez,Michael P Murphy,Paolo E Porporato,Pierre Sonveaux
View all publications

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