For the best experience on the Abcam website please upgrade to a modern browser such as Google Chrome

Hello. We're improving abcam.com and we'd welcome your feedback.

Hello. We're improving abcam.com and we'd welcome your feedback.

Infomation icon

We haven't added this to the BETA yet

New BETA website

New BETA website

Hello. We're improving abcam.com and we'd welcome your feedback.

Take a look at our BETA site and see what we’ve done so far.

Switch on our new BETA site

Now available

Search and browse selected products

  • A selection of primary antibodies

Purchase these through your usual distributor

In the coming months

  • Additional product types
  • Supporting content
  • Sign in to your account
  • Purchase online
United States
Your country/region is currently set to:

If incorrect, please enter your country/region into the box below, to view site information related to your country/region.

Call (888) 77-ABCAM (22226) or contact us
Need help? Contact us

  • My account
  • Sign out
Sign in or Register with us

Welcome

Sign in or

Don't have an account?

Register with us
My basket
Quick order
Abcam homepage

  • Research Products
    By product type
    Primary antibodies
    Secondary antibodies
    ELISA and Matched Antibody Pair Kits
    Cell and tissue imaging tools
    Cellular and biochemical assays
    Proteins and Peptides
    By product type
    Proteomics tools
    Agonists, activators, antagonists and inhibitors
    Cell lines and Lysates
    Multiplex miRNA assays
    Multiplex Assays
    By research area
    Cancer
    Cardiovascular
    Cell Biology
    Epigenetics
    Metabolism
    Developmental Biology
    By research area
    Immunology
    Microbiology
    Neuroscience
    Signal Transduction
    Stem Cells
  • Customized Products & Partnerships
    Customized Products & Partnerships

    Customized products and commercial partnerships to accelerate your diagnostic and therapeutic programs.

    Customized products

    Partner with us

  • Support
    Support hub

    Access advice and support for any research roadblock

    View support hub

    Protocols

    Your experiments laid out step by step

    View protocols

  • Events
    • Conference calendar
    • Cancer
    • Cardiovascular
    • Epigenetics & Nuclear signaling
    • Immunology
    • Neuroscience
    • Stem cells
    • Tradeshows
    • Scientific webinars
    Keep up to date with the latest events

    Full event breakdown with abstracts, speakers, registration and more

    View global event calendar

  • Pathways
    Cell signalling pathways

    View all pathways

    View all interactive pathways

  1. Link

    products/assay-kits/jc-10-mitochondrial-membrane-potential-assay-kit-microplate-ab112134.pdf

  1. Send me a copy of this email
    I agree to the terms and conditions.
Cell Biology Apoptosis Mitochondrial
Share by email

JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (ab112134)

  • Datasheet
  • SDS
  • Protocol Booklet
Reviews (2)Q&A (18)References (33)

Product price, shipping and contact information

Currently unavailable

Sorry, we can't display this right now.

Please contact us to place your order, or try again later.

 

Loading size & price…

 

Shipping and order information

Shipping info

Promotion Information

Abpromise

Guaranteed product quality, expert customer support.

Find out more.

Mitochondrial membrane potential was measured using ab112134
  • Functional Studies - JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (ab112134)

Key features and details

  • Detection method: Fluorescent
  • Platform: Microplate reader
  • Assay time: 1 hr
  • Sample type: Adherent cells, Suspension cells

You may also be interested in

ELISA
Product image
Human Frataxin ELISA Kit (ab176112)
Primary
Product image
Anti-NSE antibody [EPR12483] (ab180943)
Primary
Product image
Anti-AIF antibody - Mitochondrial Marker (ab1998)

View more associated products

Overview

  • Product name

    JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate)
    See all Mitochondrial Membrane Potential kits
  • Detection method

    Fluorescent
  • Sample type

    Adherent cells, Suspension cells
  • Assay time

    1h 00m
  • Product overview

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

  • Notes

    A microplate reader with bottom-reading mode is essential to perform this assay.

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

    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
    100X JC-10 in DMSO 1 x 250µl
    Assay Buffer A 1 x 25ml
    Assay Buffer B 1 x 25ml
  • 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

Associated products

  • Assay kits

    • JC-10 Mitochondrial Membrane Potential Assay Kit (Flow Cytometry) (ab112133)
    • JC-1 - Mitochondrial Membrane Potential Assay Kit (ab113850)
    • TMRE-Mitochondrial Membrane Potential Assay Kit (ab113852)
  • Related Products

    • JC-1, Mitochondrial membrane potential dye (ab141387)

Images

  • Mitochondrial membrane potential was measured using ab112134
    Mitochondrial membrane potential was measured using ab112134Kysenius 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/

    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.

  • Functional Studies - JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate) (ab112134)
    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.

Protocols

  • Protocol Booklet

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download

References (33)

Publishing research using ab112134? Please let us know so that we can cite the reference in this datasheet.

ab112134 has been referenced in 33 publications.

  • Fathi A  et al. Chemically induced senescence in human stem cell-derived neurons promotes phenotypic presentation of neurodegeneration. Aging Cell 21:e13541 (2022). PubMed: 34953016
  • Younes N  et al. JC-10 probe as a novel method for analyzing the mitochondrial membrane potential and cell stress in whole zebrafish embryos. Toxicol Res (Camb) 11:77-87 (2022). PubMed: 35237413
  • Capeloa T  et al. MitoQ Inhibits Human Breast Cancer Cell Migration, Invasion and Clonogenicity. Cancers (Basel) 14:N/A (2022). PubMed: 35326667
  • Mathuram TL  et al. A Synthetic Small RNA Homologous to the D-Loop Transcript of mtDNA Enhances Mitochondrial Bioenergetics. Front Physiol 13:772313 (2022). PubMed: 35464086
  • Li P  et al. Growth Differentiation Factor 15 Protects SH-SY5Y Cells From Rotenone-Induced Toxicity by Suppressing Mitochondrial Apoptosis. Front Aging Neurosci 14:869558 (2022). PubMed: 35721026
View all Publications for this product

Customer reviews and Q&As

Show All Reviews Q&A
Submit a review Submit a question

1-10 of 20 Abreviews or Q&A

JC-10

Good Good 4/5 (Ease of Use)
Abreviews
Abreviews
This JC-10 kit is useful and it is better than JC1. But the price is too high, in order to get good data, I have to buy it multiple times.
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

MISS. Urs Duthaler

Verified customer

Submitted Jul 05 2022

JC-10 Mitochondrial Membrane Potential Assay Kit (Microplate)

Excellent Excellent 5/5 (Ease of Use)
Abreviews
Abreviews
Very impress that this kit works from the first trial. Highly recommended, easy to follow, great instructions and a few step to do.
However i tested only with FCCP and CCP compound in 384w plate format. I hope to get the same impression once I run in HCS.
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Anabel de la Garza

Verified customer

Submitted Dec 24 2019

Question

I am currently using your JC-10 assay kit (ab112134). My colleague recommended the Mito-ID membrane potential cytotoxicity kit (please see product sheet attached). Enzo compares its sensitivity with JC-1, from which JC-10 has been developed as far as I understood. Do you have information how the sensitivity of the JC-10 assay kit compares to the Mito-ID assay kit?

Also, do you have any data on the JC-10 assay for primary mouse neurons? Performing the assay I get quite a big standard deviation, which makes it difficult to identify subtle differences between samples.

Read More

Abcam community

Verified customer

Asked on Dec 23 2014

Answer

Thank you for your enquiry.

JC-1, a lipophiliccationic dye, is widely used to detect mitochondrial de-polarization. However it has poor water solubility which means it precipitates in aqueous buffer even at 1 μM concentration. Compared to JC-1, JC-10 has much better water solubility. As in the case of JC-1, JC-10 is capable of entering selectively into mitochondria, and changes reversibly its color from green to orange as membrane potentials increase.

From assays performed on a fluorescence plate reader and fluorescence microscope, JC-10 outperforms JC-1 in several different cell types (e.g., primary rat hepatocytes, CHO-K1, HeLa, Jurkatand HepG2 cell lines). In most of the cell lines JC-10 has superior signal to background ratios. JC 10 also has smaller assay deviations due to its enhanced water solubility and higher sensitivity.

I am sorry we have no data from primary mouse neurons specifically in this case.

If you have some concerns regarding the results, please do not hesitate to contact me again with further details. The kit is covered by our 12 month guarantee and I will be pleased to provide further support. I would appreciate if it is possible to send:

1. Details of sample preparation.

2. The protocol used, and instrument used for reading.

3. A copy of the data.

I hope this will be helpful. I look forward to hearing from you with the requested information.

Read More

Sam Washer

Abcam Scientific Support

Answered on Dec 23 2014

Question

Do you have to remove treatment media prior to step C.3 when you add the JC-10 loading dye or do you add the dye to the media already in the plate to give a final volume of 150ul?

Read More

Abcam community

Verified customer

Asked on Sep 11 2014

Answer

You will not remove the treatment media prior to step C3.
The final volume in the well is 200 uL (100 uL cells + 50 uL JC-10 + 50 uL assay buffer B).

Read More

Jeremy Kasanov

Abcam Scientific Support

Answered on Sep 11 2014

Question

What is the function of assay buffer B?

Read More

Abcam community

Verified customer

Asked on Jul 16 2014

Answer

Assay Buffer B is used to quench the reaction and reduce the overall background. It is not necessary to perform the assay successfully however, it will definitely improve the results.

Read More

Jared Kaminski

Abcam Scientific Support

Answered on Jul 16 2014

Question

Is phenol red compatible with this assay?

Read More

Abcam community

Verified customer

Asked on Mar 05 2014

Answer

Phenol red should be OK; in our experience there has not been any interference.

Read More

Jared Kaminski

Abcam Scientific Support

Answered on Mar 05 2014

Question

What is the concentration of the 100X JC-10 solution and what is the solubility of JC-10 in DMSO?

Read More

Abcam community

Verified customer

Asked on Jun 07 2013

Answer

The concentration of 100X JC-10 in ab112134 is 3 mM. The solubility is ˜ 5mg/mL in DMSO.

Read More

Abcam Scientific Support

Answered on Jun 07 2013

Question

Thank you for your reply and helpful advices.

I checked the background :

Control well medium +all reagents (including JC-1)

Control well medium+ assay buffer A+B (without JC-1)

Control well medium + only assay buffer A

Control well medium + only assay buffer B

Only medium



You can find that in medium + all reagents the fluorescent intensity is extremely high compare to other background samples. We think that not all the JC-10 is quenched and this may cause to the high fluorescence reading of the background sample.

Did you get similar results when you checked the kit?

Do you have any other explanation?

You can find attached Excel file containing the results

Thanks,

Read More

Abcam community

Verified customer

Asked on May 01 2013

Answer



I can confirm that the numbers seems to be alright to me.

The product is used for mitochondria membrane potential measurement.

The dye needs to get into the live cells to exhibit either green (in cytosol) or red (in mitochondria) fluorescence.

Therefore just the solution alone might have some green (monomer) or red (aggregates) fluorescence. This fluorescence has no informational value.

When the mitochondria membrane potential changes, the ratio of the fluorescence in green and red changes. This is the read out the kit provides.

Please read the signal form the bottom of the cell and do not subtract the background signal for the above reasons.

Read More

Abcam Scientific Support

Answered on May 01 2013

Question

Regarding ab112134, what is the way to measure the blank? should it be growth medium only? Could you please explain how to make sense of the measurements? How do you go from fluorescence values to calculating apoptotic cells percentage? Thank you for your kind help.

Read More

Abcam community

Verified customer

Asked on Dec 27 2012

Answer

Thank you for contacting us about ab112134. Here is some further information: - The blank contains no cells and is growth media only. This gives the background and should be subtracted from all readings. - The control sample should have cells with no treatment. - ex/em = 490/520 (for green) and ex/em = 540/590 (for red) - The data is presented as a ratio of apoptotic (green) / normal cells (red). Therefore divide the 520 emission reading by the 590 emission reading. - In the graph, the ratio for control cells is set as 100%, and other ratio readings are shown relative to that, to show the proportion increase/decrease in apoptosis. I hope this information is helpful. Please do not hesitate to contact me should you have further questions.

Read More

Abcam Scientific Support

Answered on Dec 27 2012

Question

Can a white, clear bottomed tissue culture plate be used?

Read More

Abcam community

Verified customer

Asked on Dec 12 2012

Answer

Yes, you can do it, although the background might increase a bit. 

Read More

Abcam Scientific Support

Answered on Dec 12 2012

1-10 of 20 Abreviews or Q&A

  •  Previous
  • 1
  • 2
  • Next 

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

Get resources and offers direct to your inbox Sign up
A-Z by research area
  • Cancer
  • Cardiovascular
  • Cell biology
  • Developmental biology
  • Epigenetics & Nuclear signaling
  • Immunology
  • Metabolism
  • Microbiology
  • Neuroscience
  • Signal transduction
  • Stem cells
A-Z by product type
  • Primary antibodies
  • Secondary antibodies
  • Biochemicals
  • Isotype controls
  • Flow cytometry multi-color selector
  • Kits
  • Loading controls
  • Lysates
  • Peptides
  • Proteins
  • Slides
  • Tags and cell markers
  • Tools & Reagents
Help & support
  • Support
  • Make an Inquiry
  • Protocols & troubleshooting
  • Placing an order
  • RabMAb products
  • Biochemical product FAQs
  • Training
  • Browse by Target
Company
  • Corporate site
  • Investor relations
  • Company news
  • Careers
  • About us
  • Blog
Events
  • Tradeshows
  • Conferences
International websites
  • abcam.cn
  • abcam.co.jp

Join with us

  • LinkedIn
  • facebook
  • Twitter
  • YouTube
  • Terms of sale
  • Website terms of use
  • Cookie policy
  • Privacy policy
  • Legal
  • Modern slavery statement
© 1998-2023 Abcam plc. All rights reserved.