Figure 1. Western blot analysis of MCM7 using anti-MCM7 antibody (M01649-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Hela whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: MDA-MB-231 whole cell lysates,
Lane 4: C6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-MCM7 antigen affinity purified monoclonal antibody (M01649-3) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). 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. Western blot analysis of MCM7 using anti-MCM7 antibody (M01649-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human K562 whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human MCF-7 whole cell lysates,
Lane 5: human 293T whole cell lysates,
Lane 6: human U2OS whole cell lysates,
Lane 7: human A549 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-MCM7 antigen affinity purified monoclonal antibody (M01649-3) at a dilution of 1:1000 and probed with a DyLight 647 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) secondary antibody (Catalog # BA1151). A specific band was detected for MCM7 at approximately 81 kDa. The expected band size for MCM7 is at 81 kDa.
Figure 3. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of human chronic tonsillitis tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of human Laryngeal squamous cell carcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 5. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of Adenocarcinoma of the colon tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 6. IF analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 7. Flow Cytometry analysis of MCF-7 cells using anti-MCM7 antibody (M01649-3).
Overlay histogram showing MCF-7 cells stained with M01649-3 (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 mouse anti-MCM7 Antibody (M01649-3) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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 |
| Immunocytochemistry/Immunofluorescence(ICC/IF): | 1:50-400 |
| 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. | |
Figure 1. Western blot analysis of MCM7 using anti-MCM7 antibody (M01649-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Hela whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: MDA-MB-231 whole cell lysates,
Lane 4: C6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-MCM7 antigen affinity purified monoclonal antibody (M01649-3) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). 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. Western blot analysis of MCM7 using anti-MCM7 antibody (M01649-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human K562 whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human MCF-7 whole cell lysates,
Lane 5: human 293T whole cell lysates,
Lane 6: human U2OS whole cell lysates,
Lane 7: human A549 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-MCM7 antigen affinity purified monoclonal antibody (M01649-3) at a dilution of 1:1000 and probed with a DyLight 647 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) secondary antibody (Catalog # BA1151). A specific band was detected for MCM7 at approximately 81 kDa. The expected band size for MCM7 is at 81 kDa.
Figure 3. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of human chronic tonsillitis tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of human Laryngeal squamous cell carcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 5. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of Adenocarcinoma of the colon tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 6. IF analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 7. Flow Cytometry analysis of MCF-7 cells using anti-MCM7 antibody (M01649-3).
Overlay histogram showing MCF-7 cells stained with M01649-3 (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 mouse anti-MCM7 Antibody (M01649-3) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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 (M01649-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Hela whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: MDA-MB-231 whole cell lysates,
Lane 4: C6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-MCM7 antigen affinity purified monoclonal antibody (M01649-3) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). 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. Western blot analysis of MCM7 using anti-MCM7 antibody (M01649-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human K562 whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human MCF-7 whole cell lysates,
Lane 5: human 293T whole cell lysates,
Lane 6: human U2OS whole cell lysates,
Lane 7: human A549 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-MCM7 antigen affinity purified monoclonal antibody (M01649-3) at a dilution of 1:1000 and probed with a DyLight 647 Conjugated AffiniPure Goat Anti-mouse IgG (H+L) secondary antibody (Catalog # BA1151). A specific band was detected for MCM7 at approximately 81 kDa. The expected band size for MCM7 is at 81 kDa.
Figure 3. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of human chronic tonsillitis tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 4. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of human Laryngeal squamous cell carcinoma tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 5. IHC analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in a paraffin-embedded section of Adenocarcinoma of the colon tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1022) as the chromogen.
Figure 6. IF analysis of MCM7 using anti-MCM7 antibody (M01649-3).
MCM7 was detected in an immunocytochemical section of PC-3 cells. The section was incubated with mouse anti-MCM7 Antibody (M01649-3) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Figure 7. Flow Cytometry analysis of MCF-7 cells using anti-MCM7 antibody (M01649-3).
Overlay histogram showing MCF-7 cells stained with M01649-3 (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 mouse anti-MCM7 Antibody (M01649-3) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-mouse IgG (BA1126) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was mouse 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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