Western blot (WB): | 1:5000-20000 |
Immunohistochemistry (IHC): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
(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 (A01195). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Raji whole cell lysates,
Lane 2: human Daudi whole cell lysates,
Lane 3: human Ramos whole cell lysates,
Lane 4: human HMy2,CIR whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HLA-DRA antigen affinity purified polyclonal antibody (A01195) 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 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 (A01195).
HLA-DRA was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human duodenal adenocarcinoma tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human laryngeal squamous cell carcinoma tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human seminoma testis tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Flow cytometry analysis of h_PBMC cell (1:100) DyLight 488 conjugated goat anti- rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).
Western blot analysis of HLA-DRA using anti-HLA-DRA antibody (A01195). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Raji whole cell lysates,
Lane 2: human Daudi whole cell lysates,
Lane 3: human Ramos whole cell lysates,
Lane 4: human HMy2,CIR whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HLA-DRA antigen affinity purified polyclonal antibody (A01195) 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 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 (A01195).
HLA-DRA was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human mammary cancer tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human duodenal adenocarcinoma tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human laryngeal squamous cell carcinoma tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody (A01195).
HLA-DRA was detected in a paraffin-embedded section of human seminoma testis tissue. The tissue section was incubated with rabbit anti-HLA-DRA Antibody (A01195) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Flow cytometry analysis of h_PBMC cell (1:100) DyLight 488 conjugated goat anti- rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).