|
Western blot analysis of Rat Cell Lysate using NR1D1 antibody. |
|
Immunohistochemical staining of Mouse brain using NR1D1 antibody. |
|
Immunohistochemical staining of human laryngeal tissue using NR1D1 antibody. |
|
Blank control (black line): Hela. Primary Antibody (green line): Rabbit Anti-NR1D1 antibody (orb6019), dilution: 1 ug/Test, Secondary Antibody (white blue line): Goat anti-rabbit IgG-AF488, dilution: 0.5 ug/Test. Isotype control (orange line): Normal Rabbit IgG, Protocol, The cells were fixed with 4% PFA (10 min at room temperature) and then permeabilized with 90% ice-cold methanol for 20 min at -20C, The cells were then incubated in 5% BSA to block non-specific protein-protein interactions for 30 min at room temperature. Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20000 events was performed. |
|
Paraformaldehyde-fixed, paraffin embedded (Mouse brain), Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min, Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes, Blocking buffer (normal goat serum) at 37C for 30 min, Antibody incubation with (NR1D1) Polyclonal Antibody, Unconjugated (orb6019) at 1:400 overnight at 4C, followed by operating according to SP Kit (Rabbit) instructions and DAB staining. |
|
Sample: BRL-3A (Rat) Cell Lysate at 40 ug, Primary: Anti-NR1D1 (orb6019) at 1/300 dilution, Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution, Predicted band size: 67 kD, Observed band size: 67 kD. |
|
Tissue/Cell: human laryngeal tissue, 4% Paraformaldehyde-fixed and paraffin-embedded, Antigen retrieval: citrate buffer (0.01M, pH6.0), Boiling bathing for 15 min, Block endogenous peroxidase by 3% Hydrogen peroxide for 30 min, Blocking buffer (normal goat serum) at 37C for 20 min, Incubation: Anti-NR1D1 Polyclonal Antibody, Unconjugated (orb6019) 1:200, overnight at 4C, followed by conjugation to the secondary antibody and DAB staining. |
|
Tissue/Cell: rat brain tissue, 4% Paraformaldehyde-fixed and paraffin-embedded, Antigen retrieval: citrate buffer (0.01M, pH6.0), Boiling bathing for 15 min, Block endogenous peroxidase by 3% Hydrogen peroxide for 30 min, Blocking buffer (normal goat serum) at 37C for 20 min, Incubation: Anti-NR1D1/REV-ERB alpha Polyclonal Antibody, Unconjugated (orb6019) 1:200, overnight at 4C, followed by conjugation to the secondary antibody and DAB staining. |