| Western blot (WB): | 1:500-2000 |
| Immunohistochemistry (IHC): | 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 c-Kit/CD117/KIT using anti-c-Kit/CD117/KIT antibody (PB9258).
Lane 1: recombinant Human C-Kit Protein 0.5ng.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-c-Kit/CD117/KIT antigen affinity purified polyclonal antibody (PB9258) 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 c-Kit/CD117/KIT at approximately 145 kDa.

Western blot analysis of c-Kit/CD117/KIT using anti-c-Kit/CD117/KIT antibody (PB9258). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HEPG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-c-Kit/CD117/KIT antigen affinity purified polyclonal antibody (PB9258) 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 c-Kit/CD117/KIT at approximately 145 kDa. The expected band size for c-Kit/CD117/KIT is at 110 kDa.

IHC analysis of c-Kit/CD117/KIT using anti-c-Kit/CD117/KIT antibody (PB9258).
c-Kit/CD117/KIT was detected in a paraffin-embedded section of human intestinal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-c-Kit/CD117/KIT Antibody (PB9258) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

Flow Cytometry analysis of K562 cells using anti-c-Kit/CD117/KIT antibody (PB9258).
Overlay histogram showing K562 cells stained with PB9258 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-c-Kit/CD117/KIT Antibody (PB9258) 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 c-Kit/CD117/KIT using anti-c-Kit/CD117/KIT antibody (PB9258).
Lane 1: recombinant Human C-Kit Protein 0.5ng.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-c-Kit/CD117/KIT antigen affinity purified polyclonal antibody (PB9258) 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 c-Kit/CD117/KIT at approximately 145 kDa.

Western blot analysis of c-Kit/CD117/KIT using anti-c-Kit/CD117/KIT antibody (PB9258). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HEPG2 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-c-Kit/CD117/KIT antigen affinity purified polyclonal antibody (PB9258) 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 c-Kit/CD117/KIT at approximately 145 kDa. The expected band size for c-Kit/CD117/KIT is at 110 kDa.

IHC analysis of c-Kit/CD117/KIT using anti-c-Kit/CD117/KIT antibody (PB9258).
c-Kit/CD117/KIT was detected in a paraffin-embedded section of human intestinal cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-c-Kit/CD117/KIT Antibody (PB9258) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

Flow Cytometry analysis of K562 cells using anti-c-Kit/CD117/KIT antibody (PB9258).
Overlay histogram showing K562 cells stained with PB9258 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-c-Kit/CD117/KIT Antibody (PB9258) 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.



