VALIDATION IMAGES
Flow cytometric analysis of A549 cells with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at a 1:100 dilution (purple) compared with an unlabeled control (cells without incubation with primary antibody; yellow).
Paraformaldehyde-fixed and paraffin-embedded Human Kidney tissue incubated with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Human Appendix tissue incubated with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) 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 Cerebellum tissue incubated with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Human Colon Cancer tissue incubated with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed and paraffin-embedded Rat Skeletal Muscle tissue incubated with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
IF(ICC) staining with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100 in SiHa cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100 in LOVO cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:100 in 293T cells (green). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
Lane 1: A549 Cells; Lane 2: 293 Cells; Lane 3: Mouse Kidney; Probed with UQCRFS1 (10C1) Monoclonal Antibody (bsm-54363R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
25 ug total protein per lane of various lysates (see on figure) probed with UQCRFS1 monoclonal antibody, unconjugated (bsm-54363R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r.t. for 60 min.