Rabbit Anti-H2BC3 Recombinant Antibody (clone 21F11) (CAT#: ZG-0718J)

Figure 1 Rabbit Anti-H2BC3 Antibody (ZG-0718J) in WB

Western Blot
Positive WB detected in Hela whole cell lysate treated by 15mM sodium butyrate for 30min
All lanes Acetyl-Histone H2B type 1-B(K20)antibody at 0.135μg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 15 KDa
Observed band size: 15 KDa

Figure 2 Rabbit Anti-H2BC3 Antibody (ZG-0718J) in ICC

Immunocytochemistry analysis of this product diluted at 1:100 and staining in Hela cells performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.

Figure 3 Rabbit Anti-H2BC3 Antibody (ZG-0718J) in IF

Immunofluorescence staining of Hela cells(treated by 15mM sodium butyrate for 30min) with this product at 1:84,counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated Goat Anti-Rabbit IgG (H+L).

Figure 4 Rabbit Anti-H2BC3 Antibody (ZG-0718J) in FC

Overlay histogram showing Hela cells stained with this product (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min.The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-rabbit IgG (H+L) at 1/200 dilution for 1 h at 4°C. Control antibody (green line) was used under the same conditions. Acquisition of>10,000 events was performed.