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AB124539

Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit

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(5 Publications)

Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit is a Sandwich (qualitative) ELISA for the measurement of Human ATP Synthase (Complex V) Profiling in Human in Cell/Tissue Extracts samples.

View Alternative Names

ATP5E, ATP5F1E, ATPase subunit epsilon, ATP synthase F1 subunit epsilon

3 Images
Sandwich ELISA - Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit (AB124539)
  • sELISA

Supplier Data

Sandwich ELISA - Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit (AB124539)

Human HepG2 cells were cultured in NARTI Zalcitabine (ddC) for 6 days to ensure a significant effect on mitochondrial DNA replication and mitochondrial protein translation, respectively. The drug reduced mitochondrial DNA levels and hence mitochondrial protein expression. As a consequence the assembly of Complexes I, III and IV were severely affected. Note that loss of the two small mitochondrial DNA encoded subunits of Complex V (ATP synthase) does not affect overall assembly. Interestingly an increase in Complex II was induced as a consequence of I, III, IV loss possibly to up regulate mitochondrial citric acid cycle function.

Sandwich ELISA - Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit (AB124539)
  • sELISA

Supplier Data

Sandwich ELISA - Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit (AB124539)

Example sample control curve of serially titrated HepG2 extract in the working range of the assay.

Sandwich ELISA - Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit (AB124539)
  • sELISA

Supplier Data

Sandwich ELISA - Human ATP Synthase ELISA Kit (Complex V) Profiling ELISA Kit (AB124539)

Human HepG2 cells were cultured in chloramphenicol for 6 days to ensure a significant effect on mitochondrial DNA replication and mitochondrial protein translation, respectively. The antibiotic inhibited mitochondrial protein translation and assembly of Complexes I and IV but had no significant effect on Complex II, III or V.

Key facts

Detection method

Colorimetric

Sample types

Tissue Extracts, Cell Lysate

Reacts with

Human

Assay type

Sandwich (qualitative)

Sensitivity

= 12 µg/mL

Range

12 - 1000 µg/mL

Assay Platform

Microplate

Reactivity data

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Product details

ATP synthase (Complex V) is the fifth enzyme of the oxidative phosphorylation (OXPHOS) system within the mitochondrial inner membrane. ATP synthase is a large protein complex of approximately 550,000 MW made up of 17 different subunits arranged in a membrane embedded proton translocating domain (F0 domain) and a soluble ATP synthesizing catalytic domain (F1 domain). Two membrane embedded subunits ATP6 (subunit a) and ATP8 (subunit 8) are encoded on mitochondrial DNA (mtDNA). All other subunits are encoded by nuclear genomic DNA, made in the cytosol, and translocated into the organelle for assembly at the inner membrane. A proton gradient generated by the other enzymes of the OXPHOS system provides the energy for ATP synthesis by a rotational catalytic method known as the binding change mechanism. ATP synthase is regulated by CabI and IF1 proteins in response to calcium concentration and mitochondrial membrane potential respectively.

ab124539 ATP synthase (Complex V) human profiling kit is an in vitro enzyme-linked immunosorbent assay (ELISA) for the comparison of ATP synthase levels or profile in cell and tissue lysates. The assay employs a capture antibody specific for human ATP synthase coated onto microplate well strips.

Samples are pipetted into the wells and ATP synthase present in the sample is bound to the wells by the immobilized antibody. The wells are washed and an anti-ATP synthase detector antibody is added. After washing away unbound detector antibody, an HRP-conjugated secondary antibody specific for the detector antibody is pipetted into the wells. The wells are again washed, an HRP substrate solution (TMB) is added to the wells and color develops in proportion to the amount of ATP synthase bound. The developing blue color is measured at 600 nm.

Optionally the reaction can be stopped by adding hydrochloric acid which changes the color from blue to yellow and the intensity can be measured at 450 nm.

Species– Human. Rat and Mouse samples are not appropriate, other species are untested.

Store all components at 4°C. This kit is stable for 6 months from receipt. Unused microplate strips should be returned to the pouch containing the desiccant and resealed.

Precision

[ { "reproducibilityType": "Inter", "sample": "Overall", "replicates": 3, "mean": null, "standardDeviation": null, "coefficientOfVariability": "3.5" }, { "reproducibilityType": "Intra", "sample": "Overall", "replicates": 4, "mean": null, "standardDeviation": null, "coefficientOfVariability": "2.3" } ]

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
+4°C

Supplementary information

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

Complex V commonly called ATP synthase plays an important role in cellular energy production. This enzyme complex exists in the inner mitochondrial membrane and is approximately 600 kDa in size. Complex V facilitates the conversion of ADP and inorganic phosphate into ATP during oxidative phosphorylation. It consists of multiple subunits including Fo and F1 components where Fo functions as a proton channel while F1 performs ATP synthesis. Complex V is ubiquitously expressed across various tissues reflecting its essential role in energy generation.
Biological function summary

Complex V is important for maintaining cellular energy homeostasis by generating ATP the cell's energy currency. It operates as part of the mitochondrial respiratory chain complex essential for efficient energy transfer and storage. This complex plays a significant role in cellular metabolism by linking the electrochemical gradient formed by protons across the inner mitochondrial membrane to the mechanical rotation of its subunits leading to ATP formation. The ATP synthase products are imperative for processes demanding high energy such as muscle contraction and biosynthetic pathways.

Pathways

Complex V integrates into major metabolic routes primarily oxidative phosphorylation and the broader mitochondrial electron transport chain. It works in conjunction with complexes I to IV facilitating energy conversion via a proton gradient and ATP generation. Complex V's role complements proteins such as cytochrome c and ubiquinone which shuttle electrons within the electron transport chain ensuring a seamless energy production process essential for aerobic respiration.

Complex V dysfunction can cause mitochondrial diseases and disorders related to energy metabolism including Leigh syndrome and mitochondrial myopathy. These conditions often result from mutations in the ATP synthase subunits leading to impaired ATP production and altered cellular functions. Additional related proteins in these diseases include NADH dehydrogenase and succinate dehydrogenase which when dysfunctional further contribute to defects in the electron transport chain compounding the energy production challenges in affected individuals.

Product protocols

Target data

Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F(1) domain and of the central stalk which is part of the complex rotary element. Rotation of the central stalk against the surrounding alpha(3)beta(3) subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits (By similarity).
See full target information ATP5F1E

Publications (5)

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

Journal of clinical medicine 9: PubMed32527005

2020

Mitochondrial Energetics and Ca2-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy.

Applications

Unspecified application

Species

Unspecified reactive species

Maria Lombardi,Davide Lazzeroni,Annalinda Pisano,Francesca Girolami,Ottavio Alfieri,Giovanni La Canna,Giulia d'Amati,Iacopo Olivotto,Ornella E Rimoldi,Chiara Foglieni,Paolo G Camici

The journal of physiological sciences : JPS 69:1005-1017 PubMed31679117

2019

Cross talk between 26S proteasome and mitochondria in human mesenchymal stem cells' ability to survive under hypoxia stress.

Applications

Unspecified application

Species

Unspecified reactive species

Ramada R Khasawneh,Ejlal Abu-El-Rub,Abdullah Omar Serhan,Bashar Omar Serhan,Hadeel Abu-El-Rub

International journal of molecular sciences 20: PubMed30717385

2019

Degradation of Mitochondria and Oxidative Stress as the Main Mechanism of Toxicity of Pristine Graphene on U87 Glioblastoma Cells and Tumors and HS-5 Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Sławomir Jaworski,Barbara Strojny,Ewa Sawosz,Mateusz Wierzbicki,Marta Grodzik,Marta Kutwin,Karolina Daniluk,André Chwalibog

Scientific reports 8:8548 PubMed29867098

2018

Mitochondrial function is impaired in the skeletal muscle of pre-frail elderly.

Applications

Unspecified application

Species

Unspecified reactive species

Pénélope A Andreux,Marcus P J van Diemen,Maxime R Heezen,Johan Auwerx,Chris Rinsch,Geert Jan Groeneveld,Anurag Singh

Journal of inherited metabolic disease 33:775-86 PubMed20865335

2010

Insights into novel cellular injury mechanisms by gene expression profiling in nephropathic cystinosis.

Applications

Unspecified application

Species

Unspecified reactive species

Poonam Sansanwal,Li Li,Szu-Chuan Hsieh,Minnie M Sarwal
View all publications
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