Blank control: Raji. Primary Antibody (green line): Rabbit Anti-IRE1 antibody (orb157705), Dilution: 1 µg/10 6 cells, Isotype Control Antibody (orange line): Rabbit IgG. Secondary Antibody: Goat anti-rabbit IgG-PE, Dilution: 1 µg/Test. Protocol, The cells were fixed with 4% PFA (10 min at room temperature) and then permeabilized with PBST for 20 min at room temperature. The cells were then incubated in 5% BSA to block non-specific protein-protein interactions for 30 min at 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 (Rat 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 (IRE1) Polyclonal Antibody, Unconjugated (orb157705) at 1:400 overnight at 4C, followed by operating according to SP Kit (Rabbit) instructionsand DAB staining.
Sample: Lane 1: Human Raji cell lysates, Lane 2: Human HeLa cell lysates, Primary: Anti-IRE1 (orb157705) at 1/1000 dilution, Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution, Predicted band size: 105 kDa, Observed band size: 135 kDa.
WB analysis of Lane 1: Human Raji cell lysates Lane 2: Human HeLa cell lysates using IRE1a antibody
IHC-P image of Rat brain tissue using IRE1a antibody
FC analysis of Raji cell lysate using IRE1a antibody
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