• Product name

    Anti-ATP5C1 antibody [2A1AA11]
    See all ATP5C1 primary antibodies
  • Description

    Mouse monoclonal [2A1AA11] to ATP5C1
  • Host species

  • Tested applications

    Suitable for: IP, WB, In-Cell ELISA, Flow Cyt, ICC/IF, IHC-Pmore details
  • Species reactivity

    Reacts with: Mouse, Rat, Cow, Human
  • Immunogen

    This information is considered to be commercially sensitive.

  • Positive control

    • This antibody gave a positive result in IHC in the following FFPE tissue: Human normal heart muscle.
  • General notes

    This antibody clone is manufactured by Abcam.

    Product was previously marketed under the MitoSciences sub-brand.

    If you require this antibody in a particular buffer formulation or a particular conjugate for your experiments, please contact orders@abcam.com or you can find further information here.

     This product was previously labelled as ATPG




Our Abpromise guarantee covers the use of ab119686 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
IP Use at an assay dependent concentration.
WB Use a concentration of 1 µg/ml. Predicted molecular weight: 33 kDa.
In-Cell ELISA Use a concentration of 1 µg/ml.
Flow Cyt Use a concentration of 1 µg/ml.

ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody.


ICC/IF Use a concentration of 1 µg/ml.
IHC-P Use a concentration of 5 µg/ml.


  • Function

    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 the central stalk which is part of the complex rotary element. The gamma subunit protrudes into the catalytic domain formed of alpha(3)beta(3). 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.
  • Tissue specificity

    Isoform Heart is expressed specifically in the heart and skeletal muscle, which require rapid energy supply. Isoform Liver is expressed in the brain, liver and kidney. Isoform Heart and Isoform Liver are expressed in the skin, intestine, stomach and aorta.
  • Sequence similarities

    Belongs to the ATPase gamma chain family.
  • Cellular localization

    Mitochondrion. Mitochondrion inner membrane.
  • Information by UniProt
  • Database links

  • Alternative names

    • ATP synthase gamma chain, mitochondrial antibody
    • ATP synthase subunit gamma antibody
    • ATP synthase subunit gamma, mitochondrial antibody
    • ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 antibody
    • ATP synthase, H+ transporting, mitochondrial F1 complex, gamma subunit antibody
    • ATP5C 1 antibody
    • ATP5C antibody
    • ATP5C1 antibody
    • ATP5CL1 antibody
    • ATPG_HUMAN antibody
    • F ATPase gamma subunit antibody
    • F-ATPase gamma subunit antibody
    • mitochondrial antibody
    • Mitochondrial ATP synthase, gamma subunit 1 antibody
    see all


  • All lanes : Anti-ATP5C1 antibody [2A1AA11] (ab119686) at 1 µg/ml

    Lane 1 : human heart homogenate lysate at 15 µg
    Lane 2 : human HepG2 cell lysate at 15 µg
    Lane 3 : human liver mitochondria lysate at 7.5 µg
    Lane 4 : rat liver mitochondria lysate at 7.5 µg
    Lane 5 : mouse liver mitochondria lysate at 7.5 µg
    Lane 6 : bovine heart mitochondria lysate at 7.5 µg

    All lanes : Goat anti-mouse HRP at 1/5000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 33 kDa

  • Immunocytochemistry using ab119686 stained HDFn cells (human). The cells were paraformaldehyde fixed (4%, 20 min) and Triton X-100 permeabilized (0.1%, 15min) with antigen retrieval. The cells were then incubated with the antibody (ab119686, 1µg/ml) for 2h at room temperature or over night at 4°C. The secondary antibody was (red) 594 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. 10% Goat serum was used as the blocking agent for all blocking steps. The target protein locates to the mitochondria.
  • Flow cytometry. Hela cells were stained with 1µg/mL anti-ATP5C1 antibody (ab119686) (blue) or an equal amount of an isotype control antibody (red) and analyzed by flow cytometry.

  • IHC image of ATP5C1 staining in Human normal heart muscle formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab119686, 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

    For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.


This product has been referenced in:

  • Krus U  et al. Pyruvate dehydrogenase kinase 1 controls mitochondrial metabolism and insulin secretion in INS-1 832/13 clonal beta-cells. Biochem J 429:205-13 (2010). Read more (PubMed: 20415663) »
  • Fogal V  et al. Mitochondrial p32 protein is a critical regulator of tumor metabolism via maintenance of oxidative phosphorylation. Mol Cell Biol 30:1303-18 (2010). Read more (PubMed: 20100866) »
See all 5 Publications for this product

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