HMOX2 | HO-2 Rabbit pAb(bs-123

P‌‌araformaldehyde-fixed, paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (HO-2) Polyclonal Antibody, Unconjugated (bs-1238R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.

Sample:
_x000D_ Brain(Rat)lysate at 30ug;
_x000D_ Liver(Rat) lysate at 30ug;
_x000D_ Primary: Anti-HO-2 (bs-1238R) at 1:200 dilution;
_x000D_ Secondary: HRP conjugated Goat Anti-Rabbit IgG(bs-0295G-HRP) at 1: 3000 dilution;
_x000D_ Predicted band size : 38kD
_x000D_ Observed band size : 38kD, 48kD
_x000D_ _x000D_

Sample:
_x000D_ Cerebrum (Mouse) Lysate at 40 ug
_x000D_ Primary: Anti- HO-2 (bs-1238R) at 1/1000 dilution
_x000D_ Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
_x000D_ Predicted band size: 36 kD
_x000D_ Observed band size: 33 kD
_x000D_

U-937 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 20% PBST for 20 min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with HO-2 Antibody(bs-1238R)at 1:500 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).