VALIDATION IMAGES
Flow cytometric analysis of sh-sy5y cells with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:50 dilution (red) compared with an unlabeled control (cells without incubation with primary antibody; black).
Rat brain lysate probed with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
IF(ICC) staining with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:100 in N2A cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:100 in SH-SY5Y 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 Mouse kidney tissue incubated with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:300, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Human kidney tissue incubated with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:300, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Mouse brain tissue incubated with PPP1R1A (6A4I) Monoclonal Antibody (bsm-52617R) at 1:300, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.