SCF Polyclonal Antibody

Mouse spleen cells were fixed with 4% PFA (10min at room temperature) and then permeabilized with 90% ice-cold methanol for 20 min. The cells were then incubated in 5% BSA to block non-specific protein-protein interactions for 30 min at room temperature. The cells were then stained with SCF Polyclonal Antibody, Unconjugated (bs-0545R) at 1:33 for 30 min at room temperature. A Goat anti-rabbit IgG-AF647 secondary antibody was used at 1ug for 40 min at room temperature. Acquisition of 10,000 events was performed. Primary antibody staining (green) is compared to compared to unstained cells (purple), secondary only (light blue), and isotype control (orange).

Sp2\/0 (Mouse myeloma cell) lysates probed with SCF Polyclonal Antibody, Unconjugated (bs-0545R) at 1:300 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:10000 for 60 min at 37˚C.

U87MG cells were fixed with 4% PFA (10min at room temperature) and then were incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature. The cells were then stained with SCF Polyclonal Antibody, Unconjugated (bs-0545R) at 1:100 for 30 min at room temperature. A Goat anti-rabbit IgG-PE (bs-0295G-PE) secondary antibody was used at 1ug for 40 min at room temperature. Acquisition of 20,000 events was performed. Primary antibody staining (green) is compared to compared to unstained cells (purple), secondary only (light blue), and isotype control (orange).

Paraformaldehyde-fixed, paraffin-embedded Rat Spleen tissue; Antigen retrieval by boiling in sodium citrate buffer (0.01M, pH6) for 15 minutes; Block endogenous peroxidase by 3% hydrogen peroxide for 30 minutes; Blocking buffer (normal goat serum) at 37\u00b0C for 20 minutes; Antibody incubation with SCF Polyclonal Antibody, Unconjugated (bs-0545R) at 1:200 overnight at 4\u00b0C, followed by a conjugated secondary antibody and DAB staining.

Paraformaldehyde-fixed, paraffin embedded Rat Brain tissue; Antigen retrieval by boiling in sodium citrate buffer (0.01M, pH6) for 15 minutes; Block endogenous peroxidase by 3% hydrogen peroxide for 30 minutes; Blocking buffer (normal goat serum) at 37\u00b0C for 20 minutes; Antibody incubation with SCF Polyclonal Antibody, Unconjugated (bs-0545R) at 1:200 overnight at 4\u00b0C, followed by a conjugated secondary antibody and DAB staining.

Lane 1: Mouse Lung lysates; Lane 2: Mouse Spleen lysates; Lane 3:Human MCF-7 cell lysates; Lane 4: Human Hela cell lysates probed with SCF Polyclonal Antibody, Unconjugated (bs-0545R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.

Hela cell; 4% Paraformaldehyde-fixed; Ice-cold methanol at -20\u2103 for 20 min; Blocking buffer (normal goat serum, C-0005) at 37\u00b0C for 20 min; Antibody incubation with (SCF) polyclonal Antibody, Unconjugated (bs-0545R) 1:100, 90 minutes at 37\u00b0C; followed by a FITC conjugated Goat Anti-Rabbit IgG antibody at 37\u00b0C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.