Figure 1. Western blot analysis of CDK1 using anti-CDK1 antibody (PB9533). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Thymus tissue lysates,
Lane 2: Rat Spleen tissue lysates,
Lane 3: MCF-7 whole cell lysates,
Lane 4: HELA whole cell lysates,
Lane 5: JURKAT whole cell lysates,
Lane 6: NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CDK1 antigen affinity purified polyclonal antibody (PB9533) 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 CDK1 at approximately 34 kDa. The expected band size for CDK1 is at 34 kDa.
Figure 2. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of Mouse Testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 3. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of rat testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 4. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 5. IF analysis of CDK1 using anti- CDK1 antibody (PB9533).
CDK1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti- CDK1 Antibody (PB9533) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
Figure 6. Flow Cytometry analysis of U937 cells using anti-CDK1 antibody (PB9533).
Overlay histogram showing U937 cells stained with PB9533 (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-CDK1 Antibody (PB9533) 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 |
| 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. | |
Figure 1. Western blot analysis of CDK1 using anti-CDK1 antibody (PB9533). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Thymus tissue lysates,
Lane 2: Rat Spleen tissue lysates,
Lane 3: MCF-7 whole cell lysates,
Lane 4: HELA whole cell lysates,
Lane 5: JURKAT whole cell lysates,
Lane 6: NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CDK1 antigen affinity purified polyclonal antibody (PB9533) 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 CDK1 at approximately 34 kDa. The expected band size for CDK1 is at 34 kDa.
Figure 2. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of Mouse Testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 3. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of rat testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 4. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 5. IF analysis of CDK1 using anti- CDK1 antibody (PB9533).
CDK1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti- CDK1 Antibody (PB9533) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
Figure 6. Flow Cytometry analysis of U937 cells using anti-CDK1 antibody (PB9533).
Overlay histogram showing U937 cells stained with PB9533 (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-CDK1 Antibody (PB9533) 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.
Figure 1. Western blot analysis of CDK1 using anti-CDK1 antibody (PB9533). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Thymus tissue lysates,
Lane 2: Rat Spleen tissue lysates,
Lane 3: MCF-7 whole cell lysates,
Lane 4: HELA whole cell lysates,
Lane 5: JURKAT whole cell lysates,
Lane 6: NIH/3T3 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CDK1 antigen affinity purified polyclonal antibody (PB9533) 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 CDK1 at approximately 34 kDa. The expected band size for CDK1 is at 34 kDa.
Figure 2. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of Mouse Testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 3. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of rat testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 4. IHC analysis of CDK1 using anti-CDK1 antibody (PB9533).
CDK1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CDK1 Antibody (PB9533) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Figure 5. IF analysis of CDK1 using anti- CDK1 antibody (PB9533).
CDK1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti- CDK1 Antibody (PB9533) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
Figure 6. Flow Cytometry analysis of U937 cells using anti-CDK1 antibody (PB9533).
Overlay histogram showing U937 cells stained with PB9533 (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-CDK1 Antibody (PB9533) 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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