VALIDATION IMAGES
Flow cytometric analysis of Huvec cells with LYVE1 (5C1) Monoclonal Antibody (bsm-52811R) at 1:50 dilution (red) compared with an unlabeled control (cells without incubation with primary antibody; black).
Lane 1: MCF-7 lysates; Probed with LYVE1 (5C1) Monoclonal Antibody (bsm-52811R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
IF(ICC) staining with LYVE1 (5C1) Monoclonal Antibody (bsm-52811R) at 1:100 in A431 cells (red). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
IF(ICC) staining with LYVE1 (5C1) Monoclonal Antibody (bsm-52811R) at 1:100 in SW480 cells (red). The nuclear counterstain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilized with 0.25% Triton X100/PBS.
Paraformaldehyde-fixed and paraffin-embedded Human spleen tissue incubated with LYVE1 (5C1) Monoclonal Antibody (bsm-52811R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Lane 1: Mouse Spleen tissue lysates; Lane 2: Mouse Blood cell lysates; Lane 3: Mouse Lymph node tissue lysates ; Lane 4: Mouse Large intestine tissue lysates ; Lane 5: Rat Thyroid gland tissue lysates ; Lane 6: Rat Spleen tissue lysates ; Lane 7: Rat Lymph node tissue lysates ; Lane 8: Rat Large intestine tissue lysates ; Lane 9: Human Huvec cell lysates ; Lane 10: Human K562 cell lysates probed with LYVE-1 Polyclonal Antibody, Unconjugated (bsm-52811R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at room temperature for 60 min.