VALIDATION IMAGES
Mouse splenocytes probed with Rabbit Anti-E cadherin Polyclonal Antibody, PE-Cy5.5 Conjugated (bs-10009R-PE-Cy5.5) at 1:50 for 40 minutes (green)compared to control cells (blue).
Image provided by One World Lab validation program. A431 cells probed with Rabbit Anti-E cadherin Polyclonal Antibody (bs-10009R) at 1:50 for 60 minutes at room temperature followed by Goat Anti-Rabbit IgG (H+L) Alexa Fluor 488 Conjugated secondary antibody.
Image provided by One World Lab validation program. U138 cells probed with Rabbit Anti-E cadherin Polyclonal Antibody (bs-10009R) at 1:50 for 60 minutes at room temperature followed by Goat Anti-Rabbit IgG (H+L) Alexa Fluor 488 Conjugated secondary antibody.
MCF-7 cells were stained with E cadherin Polyclonal Antibody, Unconjugated(bs-10009R) at 1:500 in PBS and incubated for two hours at 37°C followed by Goat Anti-Rabbit IgG (H+L) Cy3 conjugated secondary antibody. DAPI staining of the nucleus was done and then detected.
Image provided by Independent Validation badge 29768.\n\nHistogram of MCF7 cells stained with Rabbit Anti-E-Cadherin Polyclonal Antibody (orange)(bs-10009R at 1:100), isotype control antibody (green), secondary antibody only (blue) and unstained (red)
Formalin-fixed and paraffin-embedded mouse intestine labeled with Anti-E cadherin/CD324 Polyclonal Antibody, Unconjugated(bs-10009R) 1:200, overnight at 4°C, The secondary antibody was Goat Anti-Rabbit IgG, Cy3 conjugated(bs-0295G-Cy3)used at 1:200 dilution for 40 minutes at 37°C.
Paraformaldehyde-fixed, paraffin embedded Human colon cancer; 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 E cadherin Polyclonal Antibody, Unconjugated (bs-10009R) at 1:400 overnight at 4°C, DAB staining.
Paraformaldehyde-fixed, paraffin embedded Human stomach; 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 E cadherin Polyclonal Antibody, Unconjugated (bs-10009R) at 1:400 overnight at 4°C, DAB staining.
Lane 1: Human A431 cell lysates; Lane 2: Human A549 cell lysates; Lane 3: Human HepG2 cell lysates probed with E cadherin Polyclonal Antibody, Unconjugated (bs-10009R) 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 (rat spinal cord); 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 (E cadherin) Polyclonal Antibody, Unconjugated (bs-10009R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Paraformaldehyde-fixed, paraffin embedded (rat liver); Antigen retrieval by microwave in sodium citrate buffer (pH6.0) ; Block endogenous peroxidase by 3% hydrogen peroxide for 30 minutes; Blocking buffer (3% BSA) at RT for 30min; Incubation with (E cadherin) Polyclonal Antibody, Unconjugated (bs-10009R) at 1:200 overnight at 4℃, followed by conjugation to the secondary antibody (labeled with HRP)and DAB staining.
Paraformaldehyde-fixed, paraffin embedded (human colon); Antigen retrieval by microwave in sodium citrate buffer (pH6.0) ; Block endogenous peroxidase by 3% hydrogen peroxide for 30 minutes; Blocking buffer (3% BSA) at RT for 30min; Incubation with (E cadherin) Polyclonal Antibody, Unconjugated (bs-10009R) at 1:200 overnight at 4℃, followed by conjugation to the secondary antibody (labeled with HRP)and DAB staining.