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    products/assay-kits/mitotox-complex-ii-oxphos-activityassay-kit-ab109904.pdf

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Signal Transduction Metabolism Mitochondrial
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MitoTox™ Complex II OXPHOS Activity Assay Kit (ab109904)

  • Datasheet
  • SDS
  • Protocol Booklet
Submit a review Q&A (4)References (3)

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MitoTox™ Complex II OXPHOS Activity Assay (ab109904)

    Key features and details

    • Assay type: Direct
    • Detection method: Colorimetric
    • Platform: Microplate reader
    • Assay time: 4 hr

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    Overview

    • Product name

      MitoTox™ Complex II OXPHOS Activity Assay Kit
      See all Complex II kits
    • Detection method

      Colorimetric
    • Assay type

      Direct
    • Assay time

      4h 00m
    • Species reactivity

      Reacts with: Mouse, Cow, Human
    • Product overview

      MitoTox™ Complex II OXPHOS Activity Assay Kit (ab109904) is designed for testing the direct inhibitory effect of compounds on Complex II activity in only 4 hours. Complex II extracted from the provided bovine heart mitochondria (a rich source of Complex II) is immunocaptured by specific antibodies on the plate. Complex II activity can be observed as decrease in absorbance at OD 600 nm. The intra-assay and inter-assay variation of this assay are both <15%.


      Inhibitory effects of compounds on Complex II activity can be tested in two different ways: 1. Screening format, where up to 23 compounds can be tested at a single concentration in triplicate; 2. Dose response (IC50) format, where two compounds known to affect Complex II activity can be tested at 11 different data points in triplicate.


      Testing for mitochondrial function has become a key aspect of drug discovery. Mitochondria can be affected by drug treatment, resulting into cardio- and hepatotoxic side effects that can lead to drug withdrawal from the market. Therefore, there is increasing emphasis on testing the impact on mitochondria early on in the drug development process to reduce failure rates during preclinical and clinical phases.

    • Notes

      Please store Succinate, Ubiquinone 2, Bovine Heart Mitochondria, DCPIP at -80°C and all other components at 4°C.

      Related products

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

    • Platform

      Microplate reader

    Properties

    • Storage instructions

      Please refer to protocols.
    • Components 96 tests
      Detergent 1 x 1ml
      12-channel reagent reservoirs 2 units
      20X Buffer 1 x 5ml
      Bovine heart mitochondria 2 x 360µl
      Complex II Activity Buffer 1 x 25ml
      DCPIP/DCIP 1 x 250µl
      Pre-coated 96-well microplate 1 x 96 tests
      Succinate 1 x 500µl
      Ubiquinone 2 1 x 60µl
    • Research areas

      • Signal Transduction
      • Metabolism
      • Mitochondrial
      • Kits/ Lysates/ Other
      • Kits
      • Cell Metabolism Kits
      • Other Metabolism Assay
      • Metabolism
      • Pathways and Processes
      • Mitochondrial Metabolism
      • Mitochondrial markers
    • Relevance

      Complex II is also called succinate ubiquinone oxidoreductase or more commonly succinate dehydrogenase complex. This complex is composed of four nuclear encoded subunits and contains a flavin (FAD), non-heme iron centers and a b-type cytochrome as prosthetic groups. It is both a component of the electron transport chain and an enzyme of the Krebs cycle. Complex II deficiencies are seen in OXPHOS genetic disease and found in a type of cancer called paraganglioma.
    • Alternative names

      • SDH
      • Succinate coenzyme Q reductase
      • Succinate dehydrogenase
    • Database links

      • Entrez Gene: 6390 Human
      • Entrez Gene: 6389 Human
      • Entrez Gene: 6391 Human
      • SwissProt: P31040 Human
      • SwissProt: P21912 Human
      • SwissProt: Q99643 Human
      • SwissProt: O14521 Human
      • SwissProt: 6392 Human

      Images

      • MitoTox™ Complex II OXPHOS Activity Assay (ab109904)
        MitoTox™ Complex II OXPHOS Activity Assay (ab109904)

        Typical dose response curve for TTFA (2-thenoyltrifluoracetone). Assay was performed following the Dose Response Assay Procedure using TTFA, a well known Complex II inhibitor. TTFA was prepared in DMSO to generate a 100 mM stock. Starting with a 500 µM final concentration in well, 1:2 serial dilutions of TTFA were generated.

      Protocols

      • Protocol Booklet

      Click here to view the general protocols

      Datasheets and documents

      • SDS download

      • Datasheet download

        Download

      References (3)

      Publishing research using ab109904? Please let us know so that we can cite the reference in this datasheet.

      ab109904 has been referenced in 3 publications.

      • Subedi A  et al. A novel inhibitor of tumorspheres reveals the activation of the serine biosynthetic pathway upon mitochondrial inhibition. FEBS Lett 593:763-776 (2019). PubMed: 30874300
      • Landry GM  et al. Diglycolic acid inhibits succinate dehydrogenase activity in human proximal tubule cells leading to mitochondrial dysfunction and cell death. Toxicol Lett 221:176-84 (2013). PubMed: 23827505
      • Lai K  et al. Integrated Compound Profiling Screens Identify the Mitochondrial Electron Transport Chain as the Molecular Target of the Natural Products Manassantin, Sesquicillin, and Arctigenin. ACS Chem Biol N/A:N/A (2012). PubMed: 23138533

      Customer reviews and Q&As

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

      1-4 of 4 Abreviews or Q&A

      Question

      I am looking for Complex I-IV activity kits to study in vitro activity inhibitors after incubating mouse, rat, and human cells with the inhibitors prior to mitochondrial extraction. I am worried that either the kit will not detect the inhibited portion of the mechanism (such as ab109721 not being affected by rotenone since it detects the dehyrogenase activity and not the ubiquinone activity which is affected by rotenone) or the inhibitory affect will be reversed following mitochondrial extraction and sample preparation. Do you have any advice or specific product recommendations?

      Read More

      Abcam community

      Verified customer

      Asked on May 17 2014

      Answer

      The kits that are the best suited for your experiment are listed below. I am having our datasheets team update the species reactivity.
      ab109903, Complex I; reactivity = Human, mouse, rat, bovine
      https://www.abcam.com/mitotox%E2%84%A2-complex-i-oxphos-activity-microplate-assay-ab109903.html
      ab109904, Complex II, reactivity = Human, mouse and bovine
      https://www.abcam.com/mitotox%E2%84%A2-complex-ii-oxphos-activity-microplate-assay-ab109904.html
      ab109905, Complex II + III, reactivity = This is an in solution assay so it will work with mitochondria from any species, provided that the mitochondria is of good quality. It will not work with homogenate – it requires purified mitochondria
      https://www.abcam.com/mitotoxtrade-complex-ii-nbsp-iii-oxphos-activity-microplate-assay-ab109905.html
      ab109906, Complex IV, reactivity = Human and bovine
      https://www.abcam.com/mitotoxtrade-complex-iv-oxphos-activity-microplate-assay-ab109906.html
      ab109907, Complex V, reactivity = Human, mouse, rat and bovine.
      https://www.abcam.com/mitotoxtrade-complex-v-oxphos-activity-microplate-assay-ab109907.html

      ab110419, Complexes I - V (contains the five kits above at a discounted price)
      https://www.abcam.com/mitotox%E2%84%A2-complete-oxphos-activity-assay-kit-5-assays-ab110419.html
      In regards to inhibitor treatment, the laboratory agrees that the effects would be reversible. See their response and recommendations below:

      If you were to treat the cells with for example rotenone, then isolate the mitochondria from rotenone treated cells, this will wash off all the rotenone from the sample during the sample prep and would simply find no inhibition detected by the assay.

      What we would recommend is to test normal mitochondria in-vitro with the inhibitor compound as it is suggested in the kit protocols above.
      The kits have a bovine heart mitochondria control, which you can use to see how the assay works (creating a positive and negative control with BHM plus or minus inhibitors).

      Then you can compare the BHM results with the results obtained with the mitochondria prepared from your cell system.
      The compound inhibitor must be present during the activity assay, otherwise the data will not reflect the immediate in vitro inhibitory effect of the compound, but more likely the downstream effect of that compound (i.e. If the compound generates as a downstream effect oxidative stress and this in turn affects the activity of one of the complexes of the electron transport chain).

      Read More

      Kevin Hanson

      Abcam Scientific Support

      Answered on May 17 2014

      Question

      What is the difference between these 2 kits? Why does one immunocapture the complex II while the other does not? Are there any advantages/disadvantages of the immunocapture? Why is the complex III kit solely called complex III when based on the description it sounds like complex II activity is also measured.

      Read More

      Abcam community

      Verified customer

      Asked on Oct 23 2013

      Answer

      ab109904 measures solely complex II, whereas ab109905 measures complexes II+III.
      We do not offer an immunocapture activity assay for Complex III only. The reason is that we have not generated an antibody capable of immunocapturing the native enzyme.

      Read More

      Kevin Hanson

      Abcam Scientific Support

      Answered on Oct 23 2013

      Question

      what is being used as detergent?

      Read More

      Abcam community

      Verified customer

      Asked on May 16 2012

      Answer

      Thank you for contacting us.

      The 10x detergent in the kit is 10% Lauryl maltoside, which can also be purchased separately as ab109857.

      I hope this information is helpful to you. Please do not hesitate to contact us if you need any more advice or information.

      Use our products? Submit an Abreview. Earn rewards!
      https://www.abcam.com/abreviews

      Read More

      Abcam Scientific Support

      Answered on May 16 2012

      Question

      Is there a specific pH that the reaction solution should be in order to measure activity? The inhibitor that I'm studying is a strong acid and has a pH around 2, but I can adjust this in the wells.

      Read More

      Abcam community

      Verified customer

      Asked on Feb 28 2012

      Answer

      Thank you for your call and for your patience while I've been in touch with the lab about ab109904.

      My contact at the lab gave the following reply: "Yes, a pH of 2 will destroy the assay. You will need to bring the pH to neutral ( 7 – 7.4) to test in the assay, and thereforeyou will have to test the salt version of the acid and not the acid directly in the assay. For example = Malonic acid is a known inhibitor of complex II (as it has been shown in the literature multiple times). We have tested in the past the effect of Potassium and Sodium Malonate (which is Malonic acid after pH has been adjusted with NaOH or KOH) and have found that Malonate (in the salt form) inhibits the activity of Complex II when tested with the MTOX2 assay."

      I hope this information is useful, but please let me know if you have any further questions and I'll be happy to help. Have a great day!

      Read More

      Abcam Scientific Support

      Answered on Feb 28 2012

      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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