Anti-pan ATPase Alpha 抗体 [M7-PB-E9]
Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control
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(9 Publications)
Mouse Monoclonal alpha 1 Sodium Potassium ATPase antibody. Suitable for IP, Flow Cyt, WB, IHC-P, ICC/IF and reacts with Mouse, Human, Rat samples. Cited in 9 publications. Immunogen corresponding to Native Full Length Protein corresponding to Sheep ATP1A1.
別名を表示する
Sodium/potassium-transporting ATPase subunit alpha-1, Na(+)/K(+) ATPase alpha-1 subunit, Sodium pump subunit alpha-1, ATP1A1
- IHC-P
Unknown
Immunohistochemistry paraffin embedded sections - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Immunohistochemistry was performed on both normal and cancer biopsies of deparaffinized Human testis tissue tissues. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1 : 200 with a mouse monoclonal antibody recognizing Sodium/Potassium ATPase alpha ab2871 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.
- IHC-P
Unknown
Immunohistochemistry paraffin embedded sections - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Immunohistochemistry was performed on both normal and cancer biopsies of deparaffinized Human tonsil tissue tissues. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1 : 200 with a mouse monoclonal antibody recognizing Sodium/Potassium ATPase alpha ab2871 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Immunocytochemistry/Immunofluorescence analysis of ATP1A2 shows staining in MCF-7 cells. ATP1A2 (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were incubated without (control) or with ab2871 (1 : 20) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Immunocytochemistry/Immunofluorescence analysis of ATP1A2 shows staining in U251 cells. ATP1A2 (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were incubated without (control) or with ab2871 (1 : 20) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
ICC/IF image of ab2871 stained MCF7 cells. The cells were 100% methanol fixed (5 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 (ab2871, 10µg/ml) overnight at +4°C. The secondary antibody (green) was 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.
- IHC-P
Unknown
Immunohistochemistry paraffin embedded sections - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Immunohistochemistry was performed on both normal and cancer biopsies of deparaffinized Human colon carcinoma tissues. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1 : 100 with a mouse monoclonal antibody recognizing Sodium/Potassium ATPase alpha ab2871 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.
- Flow Cyt
Unknown
Flow Cytometry - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Overlay histogram showing HEK293 cells stained with ab2871 (red line). The cells were fixed with 80% methanol (5 min) and incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab28711, 1/100 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
Please note that Abcam do not have any data for use of this antibody on non-fixed cells. We welcome any customer feedback.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-pan ATPase Alpha antibody [M7-PB-E9] - Plasma Membrane Loading Control (AB2871)
Immunocytochemistry/Immunofluorescence analysis of ATP1A2 shows staining in HeLa cells. ATP1A2 (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were incubated without (control) or with ab2871 (1 : 20) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
Reactivity data
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
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補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Different subunits of ATPase Alpha are important for cellular energy metabolism and are part of a larger enzymatic complex. This complex facilitates proton translocation in cellular organelles contributing to energy conversion processes. Through ATP hydrolysis this protein helps maintain ion gradients which are employed by cells for multiple functions such as nutrient uptake and pH balance. The machinery provided by ATPase Alpha is vital for cell survival and function.
Pathways
The activity of ATPase Alpha integrates into significant metabolic pathways such as oxidative phosphorylation and glycolysis. It is central in energy transduction providing ATP required for many cellular activities. The protein modulates activity in conjunction with other components like the cytochrome c oxidase complex in the mitochondrial electron transport chain playing a role in producing the cell's energy currency. Pan ATPase Alpha's ability to interface with glycolysis allows cells to effectively manage energy production and consumption.
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文献 (9)
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Neuropathology and applied neurobiology 48:e12811 PubMed35274343
2022
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International journal of molecular sciences 23: PubMed35008753
2021
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International journal of molecular sciences 22: PubMed34066474
2021
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Frontiers in neuroscience 13:831 PubMed31440132
2019
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British journal of pharmacology 176:787-800 PubMed30592786
2019
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The Journal of pathology 246:217-230 PubMed29984492
2018
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Diabetes 60:2598-607 PubMed21852673
2011
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IHC-Fr, WB
Species
Human, Human
Nano letters 9:4489-93 PubMed19807066
2009
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Unspecified application
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Human
Biochimica et biophysica acta 719:413-23 PubMed6295504
1982
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