ACE2 rabbit polyclonal antibody

Lane 1: Mouse Testis lysates; Lane 2:Mouse Ovary lysates; Lane 3: SH-SY5Y cell lysates; Lane 4: HepG2 cell lysates; Lane 5: A431 cell lysates probed with ACE2 Polyclonal Antibody, Unconjugated (bs-23444R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.

Lane 1:Human ACE2 Protein Overexpression E.coli Lysates; Lane 2: Control group E.coli Lysates probed with ACE2 Polyclonal Antibody, Unconjugated (bs-23444R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.

HepG2 cells(black) were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with ACE2 Polyclonal Antibody(bs-23444R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).

Lane 1: ACE2 knockout (KO) A549 cell lysates; Lane 2: Human A549 cell (Control) lysates probed with ACE2 Polyclonal Antibody, Unconjugated (bs-23444R) at 1:1000 dilution and 4\u00b0C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.

A431 cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37\u00b0C for 20 min; Antibody incubation with (ACE2) polyclonal Antibody, Unconjugated (bs-23444R) 1:100, 90 minutes at 37\u00b0C; followed by a conjugated Goat Anti-Rabbit IgG antibody at 37\u00b0C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.