Western blot analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: 293T whole cell lysates,
Lane 3: A549 whole cell lysates,
Lane 4: HEPG2 whole cell lysates,
Lane 5: CACO-2 whole cell lysates,
Lane 6: U937 whole cell lysates,
Lane 7: PC-3 whole cell lysates,
Lane 8: HL-60 whole cell lysates,
Lane 9: rat liver tissue lysates,
Lane 10: rat heart tissue lysates,
Lane 11: mouse liver tissue lysates,
Lane 12: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NDUFB8 antigen affinity purified polyclonal antibody (A07936-1) 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 NDUFB8 at approximately 19-22 kDa. The expected band size for NDUFB8 is at 22 kDa.
IHC analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human Laryngeal squamous cell carcinomas tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human renal clear cell carcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human SM fatty carcinoma of the left kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of mouse brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of rat brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
ICC/IF analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) at a dilution of 1:100. Fluoro488 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 HEL cells using anti-NDUFB8 antibody (A07936-1).
Overlay histogram showing HEL cells stained with A07936-1 (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-NDUFB8 Antibody (A07936-1) at 1:100 dilution for 30 min at 20°C. Fluoro488 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 |
| 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: 293T whole cell lysates,
Lane 3: A549 whole cell lysates,
Lane 4: HEPG2 whole cell lysates,
Lane 5: CACO-2 whole cell lysates,
Lane 6: U937 whole cell lysates,
Lane 7: PC-3 whole cell lysates,
Lane 8: HL-60 whole cell lysates,
Lane 9: rat liver tissue lysates,
Lane 10: rat heart tissue lysates,
Lane 11: mouse liver tissue lysates,
Lane 12: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NDUFB8 antigen affinity purified polyclonal antibody (A07936-1) 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 NDUFB8 at approximately 19-22 kDa. The expected band size for NDUFB8 is at 22 kDa.
IHC analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human Laryngeal squamous cell carcinomas tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human renal clear cell carcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human SM fatty carcinoma of the left kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of mouse brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of rat brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
ICC/IF analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) at a dilution of 1:100. Fluoro488 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 HEL cells using anti-NDUFB8 antibody (A07936-1).
Overlay histogram showing HEL cells stained with A07936-1 (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-NDUFB8 Antibody (A07936-1) at 1:100 dilution for 30 min at 20°C. Fluoro488 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: 293T whole cell lysates,
Lane 3: A549 whole cell lysates,
Lane 4: HEPG2 whole cell lysates,
Lane 5: CACO-2 whole cell lysates,
Lane 6: U937 whole cell lysates,
Lane 7: PC-3 whole cell lysates,
Lane 8: HL-60 whole cell lysates,
Lane 9: rat liver tissue lysates,
Lane 10: rat heart tissue lysates,
Lane 11: mouse liver tissue lysates,
Lane 12: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NDUFB8 antigen affinity purified polyclonal antibody (A07936-1) 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 NDUFB8 at approximately 19-22 kDa. The expected band size for NDUFB8 is at 22 kDa.
IHC analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human Laryngeal squamous cell carcinomas tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human renal clear cell carcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of human SM fatty carcinoma of the left kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of mouse brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) 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 NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in a paraffin-embedded section of rat brain tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
ICC/IF analysis of NDUFB8 using anti-NDUFB8 antibody (A07936-1).
NDUFB8 was detected in an immunocytochemical section of HepG2 cells. The section was incubated with rabbit anti-NDUFB8 Antibody (A07936-1) at a dilution of 1:100. Fluoro488 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 HEL cells using anti-NDUFB8 antibody (A07936-1).
Overlay histogram showing HEL cells stained with A07936-1 (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-NDUFB8 Antibody (A07936-1) at 1:100 dilution for 30 min at 20°C. Fluoro488 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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