Histone H2B Recombinant Antibody

A431 cells were stained with Histone H2B (3A6) Monoclonal Antibody (bsm-52099R) at [1:200] incubated overnight at 4C, followed by secondary antibody incubation, DAPI staining of the nuclei and detection.

Paraformaldehyde-fixed, paraffin embedded mouse liver; Antigen retrieval by boiling in sodium citrate buffer (pH6) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 30 minutes; Blocking buffer (normal serum) at 37°C for 20min; Antibody incubation with Histone H2B (3A6) Monoclonal Antibody (bsm-52099R) at 1:50 overnight at 4°C, followed by a conjugated secondary and DAB staining.

Paraformaldehyde-fixed and paraffin-embedded Human Liver tissue incubated with Histone H2B (3A6) Monoclonal Antibody (bsm-52099R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.

A431 cells(black) were fixed with 4% PFA for 10min at room temperature,permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with Histone H2B Antibody(bsm-52099R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).