Western blot analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Raji whole cell lysates,
Lane 2: Daudi whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-HLA-DRA antigen affinity purified monoclonal antibody (M01195-3) 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 HLA-DRA at approximately 36 kDa. The expected band size for HLA-DRA is at 29 kDa.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA 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-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human Mammary infiltrate tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human tonsil tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of Daudi cells using anti-HLA-DRA antibody (M01195-3).
Overlay histogram showing Daudi cells stained with M01195-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 |
| Flow Cytometry (Fixed): | 1:50-200 |
| Immunohistochemistry (IHC): | 1:50-400 |
| (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 HLA-DRA using anti-HLA-DRA antibody (M01195-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Raji whole cell lysates,
Lane 2: Daudi whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-HLA-DRA antigen affinity purified monoclonal antibody (M01195-3) 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 HLA-DRA at approximately 36 kDa. The expected band size for HLA-DRA is at 29 kDa.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA 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-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human Mammary infiltrate tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human tonsil tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of Daudi cells using anti-HLA-DRA antibody (M01195-3).
Overlay histogram showing Daudi cells stained with M01195-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Raji whole cell lysates,
Lane 2: Daudi whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-HLA-DRA antigen affinity purified monoclonal antibody (M01195-3) 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 HLA-DRA at approximately 36 kDa. The expected band size for HLA-DRA is at 29 kDa.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA 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-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human Mammary infiltrate tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human rectal cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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 HLA-DRA using anti-HLA-DRA antibody (M01195-3).
HLA-DRA was detected in a paraffin-embedded section of human tonsil tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-HLA-DRA Antibody (M01195-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
Flow Cytometry analysis of Daudi cells using anti-HLA-DRA antibody (M01195-3).
Overlay histogram showing Daudi cells stained with M01195-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with mouse anti-HLA-DRA Antibody (M01195-3) 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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