Western blot analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat heart tissue lysates,
Lane 2: rat brain tissue lysates,
Lane 3: rat lung tissue lysates,
Lane 4: rat H9C2(2-1) whole cell lysates,
Lane 5: mouse heart tissue lysates,
Lane 6: mouse brain tissue lysates,
Lane 7: mouse lung tissue lysates,
Lane 8: mouse NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified polyclonal antibody (A32267-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ATP5F1A at approximately 55 kDa. The expected band size for ATP5F1A is at 60 kDa.
Western blot analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: SK-OV-3 whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: HK-60 whole cell lysates,
Lane 4: RT4 whole cell lysates,
Lane 5: Daudi whole cell lysates,
Lane 6: THP-1 whole cell lysates,
Lane 7: HepG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified polyclonal antibody (A32267-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ATP5F1A at approximately 55 kDa. The expected band size for ATP5F1A is at 60 kDa.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human endometrial adenocarcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human thyroid cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- ATP5F1A antibody (A32267-2). detected in paraffin-embedded section of human colon cancer tissue. The tissue section were stained using the Dylight550-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1135) and counterstained with DAPI (blue).
all(11) 
IF analysis using anti- ATP5F1A antibody (A32267-2). detected in paraffin-embedded section of human placenta tissue. The tissue section were stained using the Dylight550-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1135) and counterstained with DAPI (blue).
all(11) 
IF analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of U937 cells using anti-ATP5F1A antibody (A32267-2).
Overlay histogram showing U937 cells stained with A32267-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
| Western blot (WB): | 1:500-2000 |
| Immunohistochemistry (IHC): | 1:50-400 |
| Immunofluorescence (IF): | 1:50-400 |
| Immunocytochemistry/Immunofluorescence(ICC/IF): | 1:50-400 |
| Flow Cytometry (Fixed): | 1:50-200 |
| Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
| (Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. | |
Western blot analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat heart tissue lysates,
Lane 2: rat brain tissue lysates,
Lane 3: rat lung tissue lysates,
Lane 4: rat H9C2(2-1) whole cell lysates,
Lane 5: mouse heart tissue lysates,
Lane 6: mouse brain tissue lysates,
Lane 7: mouse lung tissue lysates,
Lane 8: mouse NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified polyclonal antibody (A32267-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ATP5F1A at approximately 55 kDa. The expected band size for ATP5F1A is at 60 kDa.
Western blot analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: SK-OV-3 whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: HK-60 whole cell lysates,
Lane 4: RT4 whole cell lysates,
Lane 5: Daudi whole cell lysates,
Lane 6: THP-1 whole cell lysates,
Lane 7: HepG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified polyclonal antibody (A32267-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ATP5F1A at approximately 55 kDa. The expected band size for ATP5F1A is at 60 kDa.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human endometrial adenocarcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human thyroid cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- ATP5F1A antibody (A32267-2). detected in paraffin-embedded section of human colon cancer tissue. The tissue section were stained using the Dylight550-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1135) and counterstained with DAPI (blue).
IF analysis using anti- ATP5F1A antibody (A32267-2). detected in paraffin-embedded section of human placenta tissue. The tissue section were stained using the Dylight550-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1135) and counterstained with DAPI (blue).
IF analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of U937 cells using anti-ATP5F1A antibody (A32267-2).
Overlay histogram showing U937 cells stained with A32267-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Western blot analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat heart tissue lysates,
Lane 2: rat brain tissue lysates,
Lane 3: rat lung tissue lysates,
Lane 4: rat H9C2(2-1) whole cell lysates,
Lane 5: mouse heart tissue lysates,
Lane 6: mouse brain tissue lysates,
Lane 7: mouse lung tissue lysates,
Lane 8: mouse NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified polyclonal antibody (A32267-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ATP5F1A at approximately 55 kDa. The expected band size for ATP5F1A is at 60 kDa.
Western blot analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: SK-OV-3 whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: HK-60 whole cell lysates,
Lane 4: RT4 whole cell lysates,
Lane 5: Daudi whole cell lysates,
Lane 6: THP-1 whole cell lysates,
Lane 7: HepG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATP5F1A antigen affinity purified polyclonal antibody (A32267-2) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ATP5F1A at approximately 55 kDa. The expected band size for ATP5F1A is at 60 kDa.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human endometrial adenocarcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in a paraffin-embedded section of human thyroid cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- ATP5F1A antibody (A32267-2). detected in paraffin-embedded section of human colon cancer tissue. The tissue section were stained using the Dylight550-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1135) and counterstained with DAPI (blue).
IF analysis using anti- ATP5F1A antibody (A32267-2). detected in paraffin-embedded section of human placenta tissue. The tissue section were stained using the Dylight550-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog#BA1135) and counterstained with DAPI (blue).
IF analysis of ATP5F1A using anti-ATP5F1A antibody (A32267-2).
ATP5F1A was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of U937 cells using anti-ATP5F1A antibody (A32267-2).
Overlay histogram showing U937 cells stained with A32267-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATP5F1A Antibody (A32267-2) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
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