HLA-DR/HLA-DRA/HLA Rabbit Polyclonal Antibody, Unconjugated

Artikelnummer: BYT-ORB570390
Artikelname: HLA-DR/HLA-DRA/HLA Rabbit Polyclonal Antibody, Unconjugated
Artikelnummer: BYT-ORB570390
Hersteller Artikelnummer: orb570390
Alternativnummer: BYT-ORB570390-100
Hersteller: Biorbyt
Wirt: Rabbit
Kategorie: Antikörper
Applikation: ELISA, FC, IHC, WB
Spezies Reaktivität: Human
Immunogen: E.coli-derived human HLA-DR/HLA-DRA recombinant protein (Position: I26-L254).
Konjugation: Unconjugated
Alternative Synonym: HLA DRA, HLA DRA1, HLA-DR, HLA-DRA, MHC class II antigen DRA
HLA-DR/HLA-DRA/HLA Rabbit Polyclonal Antibody
Klonalität: Polyclonal
Konzentration: 500 µg/ml
Molekulargewicht: 37 kDa
UniProt: P01903
Puffer: Each vial contains 4mg Trehalose, 0.9mg NaCl, 0.2mg Na2HPO4, 0.05mg NaN3.
Formulierung: Lyophilized
Target-Kategorie: HLA class II histocompatibility antigen, DR alpha chain
Application Verdünnung: Western blot, 0.25-0.5µg/ml, Human Immunohistochemistry (Paraffin-embedded Section), 0.5-1µg/ml, Human Flow Cytometry (Fixed), 1-3µg/1x10 6 cells, Human ELISA, 0.1-0.5µg/ml, -
Flow Cytometry analysis of human PBMC cells using anti-HLA-DRA antibody. Overlay histogram showing human PBMC cells (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-HLA-DRA Antibody (1 µg/1x10 6 cells) for 30 min at 20C. DyLight488 conjugated goat anti-rabbit IgG (5-10 µg/1x10 6 cells) was used as secondary antibody for 30 minutes at 20C. Isotype control antibody (Green line) was rabbit IgG (1 µg/1x10 6) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
Flow Cytometry analysis of SW620 cells using anti-HLA-DRA antibody. Overlay histogram showing SW620 cells (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-HLA-DRA Antibody (1 µg/1x10 6 cells) for 30 min at 20C. DyLight488 conjugated goat anti-rabbit IgG (5-10 µg/1x10 6 cells) was used as secondary antibody for 30 minutes at 20C. Isotype control antibody (Green line) was rabbit IgG (1 µg/1x10 6) used under the same conditions. Unlabelled sample (Red line) was also used as a control.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody. HLA-DRA was detected in paraffin-embedded section of human duodenal adenocarcinoma tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 µg/ml rabbit anti-HLA-DRA Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody. HLA-DRA was detected in paraffin-embedded section of human laryngeal squamous cell carcinoma tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 µg/ml rabbit anti-HLA-DRA Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody. HLA-DRA was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 µg/ml rabbit anti-HLA-DRA Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody. HLA-DRA was detected in paraffin-embedded section of human mammary cancer tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1 µg/ml rabbit anti-HLA-DRA Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC analysis of HLA-DRA using anti-HLA-DRA antibody. HLA-DRA was detected in paraffin-embedded section of human seminoma testis tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieva