Anti-ATPB抗体[4.3E8.D10] - Mitochondrial Marker
Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker
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1
(1 Review)
|
(19 Publications)
Mouse Monoclonal ATPB antibody. Mitochondrion marker. Suitable for IP, WB, ICC/IF and reacts with Rat, Human, Mouse samples. Cited in 19 publications.
查看别名
ATP5B, ATPMB, ATPSB, ATP5F1B, ATP synthase F1 subunit beta
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
ICC/IF image of ab5432 stained HeLa cells. The cells were 4% PFA 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 (ab5432, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 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.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
Immunofluorescent analysis of ATPB in HeLa cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a ATPB monoclonal antibody (ab5432) at a dilution of 1 : 200 overnight at 4 C and incubated with a DyLight-488 conjugated secondary antibody. ATPB staining (green) F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
Immunocytochemistry analysis of ATPB using ab5432 at 5μg/mL concentration shows staining in 4% paraformaldehyde-fixed 3T3 Cells. Secondary was Goat anti-Mouse IgG (H+L) Superclonal Secondary Antibody, Alexa Fluor® 488 conjugate at 1/1000 dilution. ATPB (green), and nuclei with Hoechst 33342 dye (blue) is shown. Negative control has no primary antibody
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
Immunofluorescent analysis of ATPB in A431 cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with a ATPB monoclonal antibody (ab5432) at a dilution of 1 : 200 overnight at 4 C and incubated with a DyLight-488 conjugated secondary antibody. ATPB staining (green) F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
Immunocytochemistry/Immunofluorescent analysis of ATPB (red) in HEK293T cells. Cells fixed with 4% formaldehyde were permeabilized and blocked with 1X PBS containing 5% BSA and 0.3% Triton X-100 for 1 hour at room temperature. Cells were probed with ab5432 at 1 : 100 overnight at 4°C in 1X PBS containing 1% BSA and 0.3% Triton X-100, washed with 1X PBS, and incubated with a fluorophore-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1 : 200 for 1 hour at room temperature. Nuclei (blue) were stained with DAPI. Images were taken on a Leica DM1000 microscope at 40X magnification.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
Immunocytochemistry/Immunofluorescence analysis of rat neuronal/glial cell culture using ab5432.
- IP
Supplier Data
Immunoprecipitation - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
ATPB was immunoprecipitated from THP-1 whole cell lysate with 5 μL ab5432.
Lane 1 : ab5432 IP in THP-1 whole cell lysate, with HRP-conjugated goat anti-mouse IgG secondary
Detection : Chemiluminescence
All lanes:
Immunoprecipitation - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (ab5432)
Predicted band size: 56 kDa
false
- IP
Unknown
Immunoprecipitation - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
Immunoprecipatation of rat neuronal/glial cell extract using ab5432.
All lanes:
Immunoprecipitation - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (ab5432)
Predicted band size: 56 kDa
false
- WB
Unknown
Western blot - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (AB5432)
All lanes:
Western blot - Anti-ATPB antibody [4.3E8.D10] - Mitochondrial Marker (ab5432) at 1 µg/mL
All lanes:
Human testis tissue lysate - total protein (<a href='/products/unavailable/human-testis-tissue-lysate-total-protein-ab30257'>ab30257</a>) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Mouse IgG H&L (HRP) preadsorbed (<a href='/products/secondary-antibodies/goat-mouse-igg-h-l-hrp-preadsorbed-ab97040'>ab97040</a>) at 1/5000 dilution
Predicted band size: 56 kDa
Observed band size: 57 kDa
true
Exposure time: 16min
反应性数据
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Anti-ATPB antibody [EPR11990] - Mitochondrial Marker
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性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存时间
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ATPB functions as part of the mitochondrial ATP synthase complex which is also known as complex V of the electron transport chain. This complex is important for maintaining cellular energy homeostasis through ATP production. ATPB contributes to the catalytic activity necessary for ATP synthesis therefore supporting various cellular processes that require energy input such as muscle contraction and active transport. The protein also plays a role in coupling the proton motive force to ATP synthesis a function critical for mitochondrial efficiency and metabolic health.
Pathways
ATPB involves itself significantly in the oxidative phosphorylation and glycolysis pathways. It partners with other proteins in the ATP synthase complex such as ATP synthase subunit alpha (ATP5A1) to effectuate the conversion of energy. In the broader scope of energy metabolism ATPB integrates with glycolysis where glycolytic end-products feed into oxidative phosphorylation sustaining the cell’s energy currency. Both pathways are important for cells especially in tissues with high energy demands like the heart and skeletal muscles.
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靶点信息
文献 (19)
Recent publications for all applications. Explore the full list and refine your search
Nature methods 19:1072-1075 PubMed36050490
2022
Applications
Unspecified application
Species
Unspecified reactive species
The EMBO journal 40:e107264 PubMed34494680
2021
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Nature computational science 1:199-211 PubMed35874932
2021
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Cancers 12: PubMed33121137
2020
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Human molecular genetics 29:2845-2854 PubMed32766765
2020
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Nature communications 11:1608 PubMed32231209
2020
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Journal of neuropathology and experimental neurology 78:88-98 PubMed30500922
2018
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Experimental physiology 104:126-135 PubMed30362197
2018
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PloS one 11:e0167910 PubMed28005946
2016
Applications
WB
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Unspecified reactive species
Journal of cell science 129:3705-3720 PubMed27566162
2016
Applications
Unspecified application
Species
Unspecified reactive species
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