VALIDATION IMAGES
Human kidney Probed with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody (bsm-52614R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
IF(ICC) staining with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody (bsm-52614R) 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 Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody (bsm-52614R) 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 Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody (bsm-52614R) 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 kidney tissue incubated with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody (bsm-52614R) 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 kidney tissue incubated with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody (bsm-52614R) at 1:100, overnight at 4°C, followed by a conjugated secondary antibody and DAB staining. Counterstained with hematoxylin.
Paraformaldehyde-fixed, paraffin embedded Rat kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody, Unconjugated (bsm-52614R) at 1:200 overnight at 4°C, DAB staining.
Paraformaldehyde-fixed, paraffin embedded Human kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody, Unconjugated (bsm-52614R) at 1:200 overnight at 4°C, DAB staining.
Paraformaldehyde-fixed, paraffin embedded Mouse kidney; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Angiotensin Converting Enzyme 2 (3F1) Monoclonal Antibody, Unconjugated (bsm-52614R) at 1:200 overnight at 4°C, DAB staining.
Lane 1: Recombinant human ACE2 protein, His & Avi (HEK293)( bs-46001P) probed with ACE2 Monoclonal Antibody, Unconjugated (bsm-52614R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.
Paraformaldehyde-fixed, paraffin embedded Human Testicles; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with ACE2 Monoclonal Antibody, Unconjugated(bsm-52614R) at 1:200 overnight at 4°C, followed by conjugation to the SP Kit (Rabbit, SP-0023) and DAB (C-0010) staining.
Paraformaldehyde-fixed, paraffin embedded Human Placenta; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with ACE2 Monoclonal Antibody, Unconjugated(bsm-52614R) at 1:200 overnight at 4°C, followed by conjugation to the SP Kit (Rabbit, SP-0023) and DAB (C-0010) staining.
25 ug total protein per lane of various lysates (see on figure) probed with ACE2 monoclonal antibody, unconjugated (bsm-52614R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r.t. for 60 min.