| Western blot (WB): | 1:500-2000 | 
| Immunohistochemistry (IHC): | 1:50-400 | 
| Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 | 
| Flow Cytometry (Fixed): | 1:50-200 | 
| (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 Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781). The sample well of each lane was loaded with 30 ug of sample under reducing conditions. 
Lane 1: human Hela whole cell lysates, 
Lane 2: human 293T whole cell lysates, 
Lane 3: human HepG2 whole cell lysates, 
Lane 4: human HT1080 whole cell lysates, 
Lane 5: rat kidney tissue lysates, 
Lane 6: rat skeletal muscle tissue lysates, 
Lane 7: mouse kidney tissue lysates, 
Lane 8: mouse skeletal muscle tissue lysates. 
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cytochrome c/CYCS antigen affinity purified polyclonal antibody (BA0781) 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 Cytochrome c/CYCS at approximately 14 kDa. The expected band size for Cytochrome c/CYCS is at 12 kDa.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a paraffin-embedded section of rat lung tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a frozen section of rat brain tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a paraffin-embedded section of human skeletal muscle tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a paraffin-embedded section of rat kidney tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IF analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781).
 Cytochrome c/CYCS was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) 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 Caco-2 cells using anti-Cytochrome c/CYCS antibody (BA0781). 
Overlay histogram showing Caco-2cells stained with BA0781 (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-Cytochrome c/CYCS Antibody (BA0781) 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 Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781). The sample well of each lane was loaded with 30 ug of sample under reducing conditions. 
Lane 1: human Hela whole cell lysates, 
Lane 2: human 293T whole cell lysates, 
Lane 3: human HepG2 whole cell lysates, 
Lane 4: human HT1080 whole cell lysates, 
Lane 5: rat kidney tissue lysates, 
Lane 6: rat skeletal muscle tissue lysates, 
Lane 7: mouse kidney tissue lysates, 
Lane 8: mouse skeletal muscle tissue lysates. 
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cytochrome c/CYCS antigen affinity purified polyclonal antibody (BA0781) 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 Cytochrome c/CYCS at approximately 14 kDa. The expected band size for Cytochrome c/CYCS is at 12 kDa.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a paraffin-embedded section of rat lung tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a frozen section of rat brain tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a paraffin-embedded section of human skeletal muscle tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781) . 
 Cytochrome c/CYCS was detected in a paraffin-embedded section of rat kidney tissue. The tissue section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

IF analysis of Cytochrome c/CYCS using anti-Cytochrome c/CYCS antibody (BA0781).
 Cytochrome c/CYCS was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-Cytochrome c/CYCS Antibody (BA0781) 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 Caco-2 cells using anti-Cytochrome c/CYCS antibody (BA0781). 
Overlay histogram showing Caco-2cells stained with BA0781 (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-Cytochrome c/CYCS Antibody (BA0781) 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.






