| 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 PKC Beta/PRKCB using anti-PKC Beta/PRKCB antibody (A01940). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human K562 whole cell lysates,
Lane 2: human HEL whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: rat brain tissue lysates,
Lane 5: rat PC-12 whole cell lysates,
Lane 6: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PKC Beta/PRKCB antigen affinity purified polyclonal antibody (A01940) 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 PKC Beta/PRKCB at approximately 77 kDa. The expected band size for PKC Beta/PRKCB is at 77 kDa.

IHC analysis of PKC Beta/PRKCB using anti-PKC Beta/PRKCB antibody (A01940) .
PKC Beta/PRKCB was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-PKC Beta/PRKCB Antibody (A01940) 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.

Flow Cytometry analysis of Jurkat cells using anti-PKC Beta/PRKCB antibody (A01940).
Overlay histogram showing Jurkat cells stained with A01940 (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-PKC Beta/PRKCB Antibody (A01940) 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 PKC Beta/PRKCB using anti-PKC Beta/PRKCB antibody (A01940). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human K562 whole cell lysates,
Lane 2: human HEL whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: rat brain tissue lysates,
Lane 5: rat PC-12 whole cell lysates,
Lane 6: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PKC Beta/PRKCB antigen affinity purified polyclonal antibody (A01940) 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 PKC Beta/PRKCB at approximately 77 kDa. The expected band size for PKC Beta/PRKCB is at 77 kDa.

IHC analysis of PKC Beta/PRKCB using anti-PKC Beta/PRKCB antibody (A01940) .
PKC Beta/PRKCB was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-PKC Beta/PRKCB Antibody (A01940) 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.

Flow Cytometry analysis of Jurkat cells using anti-PKC Beta/PRKCB antibody (A01940).
Overlay histogram showing Jurkat cells stained with A01940 (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-PKC Beta/PRKCB Antibody (A01940) 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.


