VALIDATION IMAGES
Formalin-fixed and paraffin embedded mouse transplant lymphoma labeled with Anti-Bcl-xL/BCL2L1/bcl-xs, Unconjugated (bs-1336R) at 1:800, followed by conjugation to the secondary antibody and DAB staining.
Rat brain lysate probed with Anti Bcl-xL/BCL2L1/bcl-xs Polyclonal Antibody, Unconjugated (bs-1336R) at 1:200 overnight at 4˚C. Followed by conjugation to secondary antibody (bs-0295G-HRP) at 1:3000 for 90 min at RT. Predicted band 26kD. Observed band size:26kD,52kD.\n
Formalin-fixed and paraffin embedded rat brain labeled with Rabbit Anti-BCL2L1 Polyclonal Antibody, Unconjugated(bs-1336R) 1:200 followed by conjugation to the secondary antibody and DAB staining\n
Paraformaldehyde-fixed, paraffin embedded Mouse brain; 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 BCL2L1 Polyclonal Antibody, Unconjugated (bs-1336R) at 1:400 overnight at 4°C, DAB staining.
A431 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 BCL2L1 Polyclonal Antibody(bs-1336R)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).
Jurkat cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 0.1% PBST for 20 min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with BCL2L1 Polyclonal Antibody(bs-1336R)at 1:100 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody 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 (BCL2L1) polyclonal Antibody, Unconjugated (bs-1336R) 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.