Western blot analysis of GPX1 using anti-GPX1 antibody (M01019-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: human U-87 whole cell lysates,
Lane 3: human THP-1 whole cell lysates,
Lane 4: human U-937 whole cell lysates,
Lane 5: human HepG2 whole cell lysates,
Lane 6: rat brain tissue lysates,
Lane 7: rat thymus tissue lysates,
Lane 8: rat lung tissue lysates,
Lane 9: rat liver tissue lysates,
Lane 10: mouse brain tissue lysates,
Lane 11: mouse thymus tissue lysates,
Lane 12: mouse lung tissue lysates,
Lane 13: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GPX1 antigen affinity purified monoclonal antibody (M01019-2) 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 GPX1 at approximately 22 kDa. The expected band size for GPX1 is at 22 kDa.
IHC analysis of GPX1 using anti-GPX1 antibody (M01019-2).
GPX1 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GPX1 Antibody (M01019-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GPX1 using anti-GPX1 antibody (M01019-2).
GPX1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GPX1 Antibody (M01019-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- GPX1 antibody (M01019-2). detected in paraffin-embedded section of human colon cancer tissue. The tissue section were stained using the Fluoro488 conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog # BA1126) and counterstained with DAPI (blue).
all(6) 
Flow Cytometry analysis of U87 cells using anti-GPX1 antibody (M01019-2).
Overlay histogram showing U87 cells stained with M01019-2 (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-GPX1 Antibody (M01019-2) at 1:100 dilution for 30 min at 20°C. Fluoro488 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.
Flow Cytometry analysis of U251 cells using anti-GPX1 antibody (M01019-2).
Overlay histogram showing U251 cells stained with M01019-2 (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-GPX1 Antibody (M01019-2) at 1:100 dilution for 30 min at 20°C. Fluoro488 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 |
| Immunohistochemistry (IHC): | 1:50-400 |
| Immunofluorescence (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. | |
Western blot analysis of GPX1 using anti-GPX1 antibody (M01019-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: human U-87 whole cell lysates,
Lane 3: human THP-1 whole cell lysates,
Lane 4: human U-937 whole cell lysates,
Lane 5: human HepG2 whole cell lysates,
Lane 6: rat brain tissue lysates,
Lane 7: rat thymus tissue lysates,
Lane 8: rat lung tissue lysates,
Lane 9: rat liver tissue lysates,
Lane 10: mouse brain tissue lysates,
Lane 11: mouse thymus tissue lysates,
Lane 12: mouse lung tissue lysates,
Lane 13: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GPX1 antigen affinity purified monoclonal antibody (M01019-2) 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 GPX1 at approximately 22 kDa. The expected band size for GPX1 is at 22 kDa.
IHC analysis of GPX1 using anti-GPX1 antibody (M01019-2).
GPX1 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GPX1 Antibody (M01019-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GPX1 using anti-GPX1 antibody (M01019-2).
GPX1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GPX1 Antibody (M01019-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- GPX1 antibody (M01019-2). detected in paraffin-embedded section of human colon cancer tissue. The tissue section were stained using the Fluoro488 conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog # BA1126) and counterstained with DAPI (blue).
Flow Cytometry analysis of U87 cells using anti-GPX1 antibody (M01019-2).
Overlay histogram showing U87 cells stained with M01019-2 (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-GPX1 Antibody (M01019-2) at 1:100 dilution for 30 min at 20°C. Fluoro488 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.
Flow Cytometry analysis of U251 cells using anti-GPX1 antibody (M01019-2).
Overlay histogram showing U251 cells stained with M01019-2 (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-GPX1 Antibody (M01019-2) at 1:100 dilution for 30 min at 20°C. Fluoro488 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 analysis of GPX1 using anti-GPX1 antibody (M01019-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: human U-87 whole cell lysates,
Lane 3: human THP-1 whole cell lysates,
Lane 4: human U-937 whole cell lysates,
Lane 5: human HepG2 whole cell lysates,
Lane 6: rat brain tissue lysates,
Lane 7: rat thymus tissue lysates,
Lane 8: rat lung tissue lysates,
Lane 9: rat liver tissue lysates,
Lane 10: mouse brain tissue lysates,
Lane 11: mouse thymus tissue lysates,
Lane 12: mouse lung tissue lysates,
Lane 13: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GPX1 antigen affinity purified monoclonal antibody (M01019-2) 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 GPX1 at approximately 22 kDa. The expected band size for GPX1 is at 22 kDa.
IHC analysis of GPX1 using anti-GPX1 antibody (M01019-2).
GPX1 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GPX1 Antibody (M01019-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GPX1 using anti-GPX1 antibody (M01019-2).
GPX1 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GPX1 Antibody (M01019-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- GPX1 antibody (M01019-2). detected in paraffin-embedded section of human colon cancer tissue. The tissue section were stained using the Fluoro488 conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog # BA1126) and counterstained with DAPI (blue).
Flow Cytometry analysis of U87 cells using anti-GPX1 antibody (M01019-2).
Overlay histogram showing U87 cells stained with M01019-2 (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-GPX1 Antibody (M01019-2) at 1:100 dilution for 30 min at 20°C. Fluoro488 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.
Flow Cytometry analysis of U251 cells using anti-GPX1 antibody (M01019-2).
Overlay histogram showing U251 cells stained with M01019-2 (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-GPX1 Antibody (M01019-2) at 1:100 dilution for 30 min at 20°C. Fluoro488 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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