Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker
- RabMAb
- Recombinant
- Lab Essentials
- 20ul selling size
- What is this?
5
(5 Reviews)
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(51 Publications)
Anti-ATP5A antibody [EPR13030(B)] (ab176569) is a rabbit monoclonal antibody detecting ATP5A in Western Blot, Flow Cytometry (Intra), IHC-P, ICC/IF. Suitable for Human, Mouse, Rat.
- Biophysical QC for unrivalled batch-batch consistency
- Over 30 publications
View Alternative Names
ATP5A, ATP5A1, ATP5AL2, ATPM, ATP5F1A, ATP synthase F1 subunit alpha
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Intracellular flow cytometric analysis of permeabilized HeLa cells labeling ATP5A using ab176569 (unpurified) at a 1/10 dilution (red) or a rabbit IgG negative control (green).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling ATP5A using ab176569 (unpurified) at a 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Immunohistochemical analysis of paraffin-embedded Human fetal heart tissue labeling ATP5A using ab176569 (unpurified) at a 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Human liver tissue sections labeling ATP5A with Purified ab176569 at 1 : 500 dilution (0.21 µg/ml). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use)was used as the secondary antibody.Negative control : PBS instead of the primary antibody.Hematoxylin was used as a counterstain.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Intracellular Flow Cytometry analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling ATP5A with purified ab176569 at 1/60 dilution (10 μg/ml) (red). Cells were fixed with 4% Paraformaldehyde. A Goat anti rabbit IgG (Alexa Fluor® 488) secondary antibody was used at 1/2000 dilution. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Immunofluorescence analysis of MCF7 cells labeling ATP5A using ab176569 (unpurified) at a 1/100 dilution (green). DAPI nuclear staining (blue).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
ab176569 (purified) staining ATP5A in HeLa (human cervix adenocarcinoma epithelial cell) by Immunocytochemistry/Immunofluorescence (ICC/IF). Cells were fixed with 4% paraformaldehyde and permeabilized n 0.1% TritonX-100. Samples were incubated with primary antibody at 1/500 dilution (4.2μg/ml). An AlexaFluor®488 Goat anti-Rabbit (ab150077) was used as a secondary antibody at 1/1000 dilution (2μg/ml). DAPI was used as a nuclear counterstain. Confocal image showing cytoplasmic staining in HeLa cells.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Rat kidney tissue sections labeling ATP5A with Purified ab176569 at 1 : 500 dilution (0.21 µg/ml). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use)was used as the secondary antibody.Negative control : PBS instead of the primary antibody.Hematoxylin was used as a counterstain.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Mouse kidney tissue sections labeling ATP5A with Purified ab176569 at 1 : 500 dilution (0.21 µg/ml). Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0). ImmunoHistoProbe one step HRP Polymer (ready to use)was used as the secondary antibody.Negative control : PBS instead of the primary antibody.Hematoxylin was used as a counterstain.
- WB
Unknown
Western blot - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
Blocking and diluting buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (ab176569) at 0.01 µg/mL
Lane 1:
HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysates at 15 µg
Lane 2:
Mouse brain lysates at 15 µg
Lane 3:
Rat brain lysates at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 60 kDa
false
- WB
Supplier Data
Western blot - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (AB176569)
All lanes:
Western blot - Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker (ab176569) at 1/1000 dilution
Lane 1:
HepG2 cell lysate at 10 µg
Lane 2:
HeLa cell lysate at 10 µg
Lane 3:
Human fetal liver lysate at 10 µg
Lane 4:
Human fetal lung lysate at 10 µg
Secondary
All lanes:
Goat anti-rabbit HRP at 1/2000 dilution
Predicted band size: 60 kDa
true
Related conjugates and formulations (6)
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Anti-ATP5A antibody [EPR13030(B)] - BSA and Azide free
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker
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HRP Anti-ATP5A antibody [EPR13030(B)] - Mitochondrial Marker
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578 PE
PE Anti-ATP5A antibody [EPR13030(B)]
Reactivity data
Product details
What is this antibody validated in?
Anti-ATP5A antibody [EPR13030(B)] (ab176569) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Intra), Flow Cytometry (Flow Cyt), Immunohistochemistry (IHC-P), Immunocytochemistry/immunofluorescence (ICC/IF) in Human, Mouse, Rat samples.
What is the molecular weight of ATP5A?
Anti-ATP5A [EPR13030(B)] (ab176569) specifically detects a band for ATP5A (UniProt: P25705) at a molecular weight of 60kDa.
Trusted by the scientific community
Anti-ATP5A [EPR13030(B)] (ab176569) was first used in a scientific publication in 2013 and has been cited over 30 times in peer-reviewed journals.
Trial sizes available!
Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 10µl. Discover our selection of trial-size antibodies.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ATP5A is essential in cellular respiration serving as a catalytic core of the F1 component of ATP synthase. As part of the multi-subunit enzyme complex ATP synthase is responsible for ATP production the primary energy currency in cells. The ATP5A subunit works in conjunction with other subunits of the enzyme oligomer to facilitate the conversion of energy released during oxidative phosphorylation into a usable form. The protein's efficiency in this biological role underpins its importance in sustaining cellular energy homeostasis.
Pathways
ATP5A plays a pivotal role in oxidative phosphorylation and the electron transport chain integral components of cellular respiration. The oxidative phosphorylation pathway depends on this protein to manage the synthesis of ATP molecules while the electron transport chain creates the proton gradient necessary for ATP production. ATP5A is functionally connected to other proteins in these pathways such as ATP5B and cytochrome c oxidase working in a coordinated manner to ensure efficient energy transfer and maintenance.
Product protocols
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Target data
Publications (51)
Recent publications for all applications. Explore the full list and refine your search
Journal of translational medicine 23:1054 PubMed41053757
2025
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Science advances 11:eady0240 PubMed40864725
2025
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Nature 646:474-482 PubMed40836094
2025
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Journal of nanobiotechnology 23:339 PubMed40340852
2025
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Translational cancer research 14:1246-1264 PubMed40104707
2025
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 12:e2408599 PubMed39656941
2024
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Cell reports. Medicine 5:101840 PubMed39626672
2024
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International journal of nanomedicine 19:9799-9819 PubMed39345912
2024
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Life science alliance 7: PubMed39209534
2024
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Frontiers in oncology 14:1427029 PubMed39206154
2024
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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