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AB109911

Complex IV Rodent Enzyme Activity Microplate Assay Kit

5

(3 Reviews)

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(105 Publications)

Complex IV Rodent Enzyme Activity Microplate Assay Kit (ab109911) is used to determine the activity of cytochrome c oxidase in mouse samples. The assay is based on antibody-based capture of Complex IV on the plate, followed by a biochemical assay.

Uses antibody capture for improved assay specificity

View Alternative Names

COX4, COX4I1, Cytochrome c oxidase polypeptide IV, Cytochrome c oxidase subunit IV isoform 1, COX IV-1

3 Images
Functional Studies - Complex IV Rodent Enzyme Activity Microplate Assay Kit (AB109911)
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PubMed

Functional Studies - Complex IV Rodent Enzyme Activity Microplate Assay Kit (AB109911)

Mitochondrial ROS dependent functional deficiency and structural impairment in cardiac mitochondria after sepsis.

Mitchondiral fractions from the heart tissue of Rats infected by S. pneumoniae, or given PBS sham control, were subjected to measurements of complex I-V activities. Complex I was measured with ab109721 (top left), Complex II + III were measured using ab109905 (top right), Complex IV was measured using ab109911 (bottom left) and Complex V was measured using ab109714 (bottom right).

Freshly isolated mitochondrial pellets were resuspened in PBS supplemented with 10% detergent provided in the kits. Protein concentrations of these mitochondrial lysates were estimated and 25 μg (for complex I, IV and V) or 100 μg (for complex II+III) mitochondrial protein was used per reaction. Enzyme activities were measured spectrophotometricly in triplicate and expressed as changes of absorbance per minute per mg protein.

Image courtesy of Yao X et al.PLoS One. 2015; 10(10): e0139416. doi: 10.1371/journal.pone.0139416.

Functional Studies - Complex IV Rodent Enzyme Activity Microplate Assay Kit (AB109911)
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Supplier Data

Functional Studies - Complex IV Rodent Enzyme Activity Microplate Assay Kit (AB109911)

To determine the activity in the sample, calculate the slope by using microplate software or by manual calculations using one of the two methods shown. Compare the sample rate with the rate of the control (normal) sample and with the rate of the null (background) to get the relative Complex IV activity. (A)The rate is determined by calculating the gradient of the initial slope over the linear region. (B) The rate is determined by calculating the slope between two points within the linear region.

Functional Studies - Complex IV Rodent Enzyme Activity Microplate Assay Kit (AB109911)
  • FuncS

Supplier Data

Functional Studies - Complex IV Rodent Enzyme Activity Microplate Assay Kit (AB109911)

Abcam's enzyme activity assays apply a novel approach, whereby target enzymes are first immunocaptured from tissue or cell samples before subsequent functional analysis. All of our ELISA kits utilize highly validated monoclonal antibodies and proprietary buffers, which are able to capture even very large enzyme complexes in their fully-intact, functionally-active states. Capture antibodies are pre-coated in the wells of premium Nunc MaxiSorp™ modular microplates, which can be broken into 8-well strips. After the target has been immobilized in the well, substrate is added, and enzyme activity is analyzed by measuring the change in absorbance of either the substrate or the product of the reaction (depending upon which enzyme is being analyzed). By analyzing the enzyme's activity in an isolated context, outside of the cell and free from any other variables, an accurate measurement of the enzyme's functional state can be understood.

Key facts

Detection method

Colorimetric

Sample types

Cell culture extracts, Tissue

Reacts with

Mouse, Rat

Assay type

Enzyme activity

Results type

Quantitative

Assay time

6h

Assay Platform

Microplate reader

Reactivity data

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Product details

Complex IV Rodent Enzyme Activity Microplate Assay Kit (ab109911) is used to determine the activity of cytochrome c oxidase in a mouse sample with speed and simplicity.

The COX enzyme is immunocaptured within the wells of the microplate and activity is determined colorimetrically by following the oxidation of reduced cytochrome c by the absorbance change at 550 nm.

Included in this kit for performance of the activity assay are buffer, detergent, substrate, and 96-well microplate with monoclonal antibody pre-bound to the wells of the plate, allowing for a stream-lined assay.

Complex IV assay protocol summary
- add samples to wells to capture enzyme and incubate for 3 hrs
- wash wells
- add reaction mix
- analyze with microplate reader in kinetic mode for 120 min

Buffer, detergent, and microplate should be stored at 4°C, Reagent C (reduced cytochrome c) should be stored at -80°C.

Range of complex IV / cytochrome c oxidase assay kits
Immunocapture with biochemical assay (plate-based) ab109911 (this kit) and ab109909.
Immunocapture with biochemical assay (dipstick) ab109878 and ab109876
Immunocapture with biochemical assay and ELISA ab109910

What's included?

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Properties and storage information

Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
Multi
Appropriate long-term storage conditions
Multi
Storage information
Please refer to protocols

Supplementary information

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

Complex IV also known as cytochrome c oxidase is an important component of the electron transport chain in mitochondria. This enzyme complex has significant mass approximately 204 kDa and operates primarily in the inner mitochondrial membrane. It catalyzes the transfer of electrons from cytochrome c to oxygen facilitating ATP generation. Complex IV is ubiquitously expressed in all tissues with higher expression in organs with high energy demands like heart and skeletal muscle. This enzyme is composed of multiple subunits encoded by both mitochondrial and nuclear DNA.
Biological function summary

Cytochrome c oxidase plays a critical role in cellular respiration. It forms part of the larger enzyme complex which also includes Complex I II and III. These complexes work together to create a proton gradient across the inner mitochondrial membrane essential for ATP synthesis via oxidative phosphorylation. This enzyme's activity is measured through assays like the cytochrome c oxidase assay which evaluates its function in various tissues. These assays help researchers understand how effectively electrons are being transferred and protons are driven across the membrane.

Pathways

Complex IV is integral to the oxidative phosphorylation pathway and the broader mitochondrial respiratory chain. It interacts closely with cytochrome c a small heme protein that shuttles electrons between Complex III (cytochrome c reductase) and Complex IV. Through these interactions the proton gradient is established enabling ATP synthase to convert chemical energy into usable cell energy. This process significantly impacts cellular metabolism and energy production influencing how efficiently cells function.

Complex IV dysfunction is associated with mitochondrial diseases and certain neurodegenerative disorders. For instance defects in cytochrome c oxidase lead to conditions like Leigh syndrome a severe neurological disorder. Also studies show that disruptions in the electron transport chain involving Complex IV relate closely to Alzheimer's disease. Alterations in proteins like cytochrome c which work in tandem with Complex IV can exacerbate these conditions highlighting the importance of this target in understanding and potentially treating these diseases.

Product protocols

Target data

Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix.
See full target information COX4I1

Publications (105)

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

Function (Oxford, England) : PubMed41627900

2026

Short-term time-restricted feeding improves metabolic rhythms and liver mitochondrial bioenergetic function in high fat diet-fed mice.

Applications

Unspecified application

Species

Unspecified reactive species

Jennifer A Valcin,Telisha Millender-Swain,Jodi R Paul,Brandon K Collins,Fatme Ghandour,Sameer Al Diffalha,Jennifer S Pollock,David M Pollock,Scott W Ballinger,Karen L Gamble,Shannon M Bailey

Nature communications 16:6105 PubMed40603847

2025

Immature Acta2 smooth muscle cells cause moyamoya-like cerebrovascular lesions in mice prevented by boosting OXPHOS.

Applications

Unspecified application

Species

Unspecified reactive species

Anita Kaw,Suravi Majumder,Jose E Esparza Pinelo,Ting Wu,Zbigniew Starosolski,Zhen Zhou,Albert J Pedroza,Xueyan Duan,Kaveeta Kaw,Angie D Gonzalez,Ripon Sarkar,Michael P Fischbein,Philip L Lorenzi,Lin Tan,Sara A Martinez,Iqbal Mahmud,Laxman Devkota,L Maximilian Buja,Heinrich Taegtmeyer,Ketan B Ghaghada,Sean P Marrelli,Callie S Kwartler,Dianna M Milewicz

Cellular and molecular neurobiology 45:60 PubMed40533653

2025

Senolytic Treatment Attenuates Global Ischemic Brain Injury and Enhances Cognitive Recovery by Targeting Mitochondria.

Applications

Unspecified application

Species

Unspecified reactive species

Caihong Gu,Ting Guo,Xiaobing Chen,Xinyu Zhou,Yong Sun

GeroScience 47:5881-5901 PubMed40111699

2025

Chronic alcohol consumption accelerates cardiovascular aging and decreases cardiovascular reserve capacity.

Applications

Unspecified application

Species

Unspecified reactive species

Partha Mukhopadhyay,Burhan Yokus,Bruno Paes-Leme,Sándor Bátkai,Zoltán Ungvári,György Haskó,Pal Pacher

The Journal of clinical investigation 135: PubMed39786963

2025

Loss of Cpt1a results in elevated glucose-fueled mitochondrial oxidative phosphorylation and defective hematopoietic stem cells.

Applications

Unspecified application

Species

Unspecified reactive species

Jue Li,Jie Bai,Vincent T Pham,Michihiro Hashimoto,Maiko Sezaki,Qili Shi,Qiushi Jin,Chenhui He,Amy Armstrong,Tian Li,Mingzhe Pan,Shujun Liu,Yu Luan,Hui Zeng,Paul R Andreassen,Gang Huang

Scientific reports 14:29371 PubMed39658563

2024

Detoxification of hydrogen sulfide by synthetic heme model compounds.

Applications

Unspecified application

Species

Unspecified reactive species

Atsuki Nakagami,Qiyue Mao,Masaki Horitani,Masahito Kodera,Hiroaki Kitagishi

Pharmacological reports : PR 77:145-157 PubMed39623245

2024

Proteomics analysis in rats reveals convergent mechanisms between major depressive disorder and dietary zinc deficiency.

Applications

Unspecified application

Species

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Łukasz Gąsior,Bartłomiej Pochwat,Monika Zaręba-Kozioł,Jakub Włodarczyk,Andreas Martin Grabrucker,Bernadeta Szewczyk

The EMBO journal 43:5941-5971 PubMed39420094

2024

An Orai1 gain-of-function tubular aggregate myopathy mouse model phenocopies key features of the human disease.

Applications

Unspecified application

Species

Unspecified reactive species

Nan Zhao,Antonio Michelucci,Laura Pietrangelo,Sundeep Malik,Linda Groom,Jennifer Leigh,Thomas N O'Connor,Takahiro Takano,Paul D Kingsley,James Palis,Simona Boncompagni,Feliciano Protasi,Robert T Dirksen

Genes & diseases 11:101100 PubMed39281832

2024

Elevated meteorin-like protein from high-intensity interval training improves heart function via AMPK/HDAC4 pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Yongshun Wang,Jie Yuan,Huadong Liu,Jie Chen,Jieru Zou,Xiaoyi Zeng,Lei Du,Xin Sun,Zhengyuan Xia,Qingshan Geng,Yin Cai,Jingjin Liu

The Journal of clinical investigation 134: PubMed38870029

2024

Exclusion of sulfide:quinone oxidoreductase from mitochondria causes Leigh-like disease in mice by impairing sulfide metabolism.

Applications

Unspecified application

Species

Unspecified reactive species

Eiki Kanemaru,Kakeru Shimoda,Eizo Marutani,Masanobu Morita,Maria Miranda,Yusuke Miyazaki,Claire Sinow,Rohit Sharma,Fangcong Dong,Donald B Bloch,Takaaki Akaike,Fumito Ichinose
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