Formalin-fixed and paraffin embedded rabbit carotid artery labeled Anti-Cyclin D3 Polyclonal Antibody, Unconjugated (bs-0660R) at 1:200, followed by conjugation to the secondary antibody and DAB staining


Molt-4 cells(black) were fixed with 4% PFA for 10min at room temperature,permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with Cyclin D3 Polyclonal Antibody(bs-0660R)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).


Hela cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (Cyclin D3) polyclonal Antibody, Unconjugated (bs-0660R) 1:100, 90 minutes at 37°C; followed by a conjugated Goat Anti-Rabbit IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.


Lane 1: Mouse Testis tissue lysates; Lane 2: Rat Testis tissue lysates probed with Cyclin D3 Polyclonal Antibody, Unconjugated (bs-0660R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.