Histone H1.4(Thr18) Polyclonal Antibody

Formalin-fixed and paraffin embedded rat brain labeled with Anti-phospho-Histone H1.4(Thr18) Polyclonal Antibody, Unconjugated (bs-3171R) at 1:200 followed by conjugation to the secondary antibody and DAB staining

Paraformaldehyde-fixed, paraffin embedded Rat liver; 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 Histone H1.4(Thr18) Polyclonal Antibody, Unconjugated (bs-3171R) at 1:200 overnight at 4°C, DAB staining.

Paraformaldehyde-fixed, paraffin embedded Rat 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 Histone H1.4(Thr18) Polyclonal Antibody, Unconjugated (bs-3171R) at 1:200 overnight at 4°C, DAB staining.

Paraformaldehyde-fixed, paraffin embedded Rat kidney; 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 Histone H1.4(Thr18) Polyclonal Antibody, Unconjugated (bs-3171R) at 1:200 overnight at 4°C, DAB staining.

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 Histone H1.4(Thr18) Polyclonal Antibody, Unconjugated (bs-3171R) at 1:200 overnight at 4°C, DAB staining.

HepG2 cells 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 phospho-Histone H1.4 (Thr18) Antibody(bs-3171R)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 incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).