Figure 1. Western blot analysis of MCM7 using anti-MCM7 antibody (PA1792). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human COLO320 whole cell lysates,
Lane 2: Human SW620 whole cell lysates,
Lane 3: Human HELA whole cell lysates,
Lane 4: Human 22RV1 whole cell lysates,
Lane 5: Human 293T whole cell lysates,
Lane 6: Human U937 whole cell lysates,
Lane 7: Human JURKAT whole cell lysates,
Lane 8: Human Raji whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MCM7 antigen affinity purified polyclonal antibody (PA1792) 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 MCM7 at approximately 81 kDa. The expected band size for MCM7 is at 81 kDa.
Figure 2. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in frozen section of MCF-7 cell. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in frozen section of Hela cell. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 5. IF analysis of MCM7 using anti-MCM7 antibody (PA1792) and anti-Alpha Tubulin antibody (M03989-3).
MCM7 was detected in an immunocytochemical section of MCF-7 cells. The section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) and Cy3-conjugated Anti-mouse IgG Secondary Antibody (red)(Catalog#BA1031) were used as secondary antibody.
Figure 6. Flow Cytometry analysis of HL-60 cells using anti-MCM7 antibody (PA1792).
Overlay histogram showing HL-60 cells stained with PA1792 (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-MCM7 Antibody (PA1792) 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 MCM7 using anti-MCM7 antibody (PA1792). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human COLO320 whole cell lysates,
Lane 2: Human SW620 whole cell lysates,
Lane 3: Human HELA whole cell lysates,
Lane 4: Human 22RV1 whole cell lysates,
Lane 5: Human 293T whole cell lysates,
Lane 6: Human U937 whole cell lysates,
Lane 7: Human JURKAT whole cell lysates,
Lane 8: Human Raji whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MCM7 antigen affinity purified polyclonal antibody (PA1792) 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 MCM7 at approximately 81 kDa. The expected band size for MCM7 is at 81 kDa.
Figure 2. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in frozen section of MCF-7 cell. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in frozen section of Hela cell. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 5. IF analysis of MCM7 using anti-MCM7 antibody (PA1792) and anti-Alpha Tubulin antibody (M03989-3).
MCM7 was detected in an immunocytochemical section of MCF-7 cells. The section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) and Cy3-conjugated Anti-mouse IgG Secondary Antibody (red)(Catalog#BA1031) were used as secondary antibody.
Figure 6. Flow Cytometry analysis of HL-60 cells using anti-MCM7 antibody (PA1792).
Overlay histogram showing HL-60 cells stained with PA1792 (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-MCM7 Antibody (PA1792) 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 MCM7 using anti-MCM7 antibody (PA1792). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human COLO320 whole cell lysates,
Lane 2: Human SW620 whole cell lysates,
Lane 3: Human HELA whole cell lysates,
Lane 4: Human 22RV1 whole cell lysates,
Lane 5: Human 293T whole cell lysates,
Lane 6: Human U937 whole cell lysates,
Lane 7: Human JURKAT whole cell lysates,
Lane 8: Human Raji whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MCM7 antigen affinity purified polyclonal antibody (PA1792) 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 MCM7 at approximately 81 kDa. The expected band size for MCM7 is at 81 kDa.
Figure 2. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 3. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in frozen section of MCF-7 cell. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of MCM7 using anti-MCM7 antibody (PA1792).
MCM7 was detected in frozen section of Hela cell. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1022) as the chromogen.
Figure 5. IF analysis of MCM7 using anti-MCM7 antibody (PA1792) and anti-Alpha Tubulin antibody (M03989-3).
MCM7 was detected in an immunocytochemical section of MCF-7 cells. The section was incubated with rabbit anti-MCM7 Antibody (PA1792) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) and Cy3-conjugated Anti-mouse IgG Secondary Antibody (red)(Catalog#BA1031) were used as secondary antibody.
Figure 6. Flow Cytometry analysis of HL-60 cells using anti-MCM7 antibody (PA1792).
Overlay histogram showing HL-60 cells stained with PA1792 (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-MCM7 Antibody (PA1792) 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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