VALIDATION IMAGES
Flow cytometric analysis of HeLa cells with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:50 dilution (red) compared with an unlabeled control (cells without incubation with primary antibody; black).
HepG2 cell lysate probed with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
IF(ICC) staining with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:300 in HeLa cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:300 in MCF-7 cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:300 in HepG2 cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
Paraformaldehyde-fixed and paraffin-embedded Human breast carcinoma tissue incubated with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Mouse pancreas tissue incubated with E2F1 (3C2) Monoclonal Antibody (bsm-52760R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.