Mouse Monoclonal MTCO1 antibody. Suitable for IP, Flow Cyt, ICC/IF and reacts with Human, Cow samples. Cited in 4 publications.
pH: 7.5
Preservative: 0.02% Sodium azide
Constituents: HEPES buffered saline
IP | Flow Cyt | WB | IHC-P | ICC/IF | |
---|---|---|---|---|---|
Human | Tested | Tested | Not recommended | Not recommended | Tested |
Cow | Tested | Expected | Not recommended | Not recommended | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 100 µg/mg of lysate | Notes - |
Species Cow | Dilution info 100 µg/mg of lysate | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1 µg for 106 Cells | Notes ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
Species | Dilution info | Notes |
---|---|---|
Species Cow | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Cow | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Cow | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 5 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Cow | Dilution info Use at an assay dependent concentration. | Notes - |
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.
COI, COXI, MTCO1, MT-CO1, Cytochrome c oxidase subunit 1, Cytochrome c oxidase polypeptide I
Mouse Monoclonal MTCO1 antibody. Suitable for IP, Flow Cyt, ICC/IF and reacts with Human, Cow samples. Cited in 4 publications.
pH: 7.5
Preservative: 0.02% Sodium azide
Constituents: HEPES buffered saline
100 µg ab109863 can capture at least 10 µg Complex IV (COX) from 1 mg solubilized Bovine heart mitochondria.
ab109863 was produced in vitro using hybridomas grown in serum-free medium, and then purified by biochemical fractionation.
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Complex IV also known as cytochrome c oxidase is a multi-subunit enzyme complex important for the electron transport chain (ETC) in mitochondria. It consists of 13 protein subunits and has an approximate mass of 204 kDa. Complex IV is located in the inner mitochondrial membrane where it facilitates the transfer of electrons from cytochrome c to molecular oxygen reducing it to water. This process helps create a proton gradient across the inner membrane which is essential for ATP production. In high-energy demand tissues like heart and skeletal muscle expression levels of Complex IV are notably higher.
Complex IV plays a critical role in cellular respiration by being the terminal enzyme of the ETC. It is part of a larger complex and its primary function is to aid in oxidative phosphorylation. This complex facilitates oxygen consumption in cells aiding ATP synthesis and influencing metabolic rate. Complex IV is involved in maintaining cellular energy homeostasis and regulation of reactive oxygen species which also contributes to cell signaling and apoptosis.
Complex IV takes a vital role in the oxidative phosphorylation and apoptosis pathways. In oxidative phosphorylation it interacts with other ETC complexes including Complex I and II to assure efficient ATP production. The role of Complex IV in apoptosis pathways involves interactions with cytochrome c which upon release into the cytosol can trigger the apoptotic machinery. These pathways are fundamental for cellular energy production and programmed cell death ensuring proper cell function and turnover.
Complex IV dysfunction is associated with mitochondrial diseases and neurodegenerative disorders. Mitochondrial diseases such as Leigh syndrome can occur due to mutations affecting Complex IV subunits leading to impaired energy production and metabolic acidosis. In neurodegenerative disorders like Alzheimer's disease altered Complex IV activity contributes to energy deficits and increased oxidative stress. Proteins like amyloid-beta have shown connections with Complex IV alterations in Alzheimer's disease hinting at a link between mitochondrial dysfunction and the pathogenesis of such disorders.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Overlay histogram showing HepG2 cells stained with ab109863 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab109863, 1μg/1x106 cells) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-mouse IgG (H+L) (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (Mouse IgG1, Kappa Monoclonal [B11/6] - Isotype Control ab91353, 1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.
ICC/IF image of ab109863 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab109863, 5μg/ml) overnight at +4°C. The secondary antibody (green) was Goat Anti-Mouse IgG H&L (DyLight® 488) preadsorbed ab96879, DyLight® 488 goat anti-mouse IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.
Staining of Complex IV Lane 1: 0.1 mg Human mitochondrial lysate
Lane 2: 0.1 mg Bovine mitochondrial lysate
Lane 3: 0.025 mg Human mitochondrial lysate
Lane 4: 0.025 mg Bovine mitochondrial lysate
Immunoprecipitated using ab109863 at 100 µg/mg lysate
All lanes: Immunoprecipitation - Anti-Complex IV Immunocapture antibody [31E91B82G9] (ab109863)
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