Western blot (WB): | 1:500-2000 |
Flow Cytometry (Fixed): | 1:50-200 |
Western blot analysis of Cyclin D1/CCND1 using anti-Cyclin D1/CCND1 antibody (BA0770-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Testis tissue lysates,
Lane 2: Human Placenta tissue lysates,
Lane 3: Rat Brain tissue lysates,
Lane 4: MCF-7 whole cell lysates,
Lane 5: COLO320 whole cell lysates,
Lane 6: SW620 whole cell lysates,
Lane 7: MM231 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cyclin D1/CCND1 antigen affinity purified polyclonal antibody (BA0770-2) 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 Cyclin D1/CCND1 at approximately 34 kDa. The expected band size for Cyclin D1/CCND1 is at 34 kDa.
Flow Cytometry analysis of U-87MG cells using anti- Cyclin D1 antibody (BA0770-2).
Overlay histogram showing U-87MG cells stained with BA0770-2 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cyclin D1 Antibody (BA0770-2, 1:100) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 1:100) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Western blot analysis of Cyclin D1/CCND1 using anti-Cyclin D1/CCND1 antibody (BA0770-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Testis tissue lysates,
Lane 2: Human Placenta tissue lysates,
Lane 3: Rat Brain tissue lysates,
Lane 4: MCF-7 whole cell lysates,
Lane 5: COLO320 whole cell lysates,
Lane 6: SW620 whole cell lysates,
Lane 7: MM231 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Cyclin D1/CCND1 antigen affinity purified polyclonal antibody (BA0770-2) 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 Cyclin D1/CCND1 at approximately 34 kDa. The expected band size for Cyclin D1/CCND1 is at 34 kDa.
Flow Cytometry analysis of U-87MG cells using anti- Cyclin D1 antibody (BA0770-2).
Overlay histogram showing U-87MG cells stained with BA0770-2 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cyclin D1 Antibody (BA0770-2, 1:100) for 30 min at 20°C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 1:100) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.