VALIDATION IMAGES
This image was generously provided by Zu Yue Deng from Zhejiang University of Technology. Human heart tissue probed with Rabbit Anti-LOX 1 Polyclonal Antibody, Unconjugated (bs-2044R). Protein bands were developed using an HRP system.
Formalin-fixed and paraffin embedded rat aorta labeled with Anti-LOX-1 Polyclonal Antibody, Unconjugated (bs-2044R) followed by conjugation to the secondary antibody and DAB staining
RSC96 cells probed with LOX 1 Polyclonal Antibody, Unconjugated (bs-2044R) at 1:100 for 30 minutes followed by incubation with a conjugated secondary (PE Conjugated) (green) for 30 minutes compared to control cells (blue), secondary only (light blue) and isotype control (orange).
Human A549 cells probed with Rabbit Anti-LOX1 Polyclonal Antibody, Unconjugated (bs-2044R) (green) at 1:20 for 30 minutes followed by a FITC conjugated secondary antibody compared to unstained cells (blue).
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 LOX 1 Polyclonal Antibody, Unconjugated (bs-2044R) at 1:500 overnight at 4°C, followed by a conjugated secondary for 20 minutes and DAB staining.
Paraformaldehyde-fixed, paraffin embedded Rabbit 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 LOX 1 Polyclonal Antibody, Unconjugated (bs-2044R) at 1:400 overnight at 4°C, DAB staining.
Lane 1: Mouse lung lysates; Lane 2: Mouse cerebrum lysates; probed with LOX 1 Polyclonal Antibody, unconjugated (bs-2044R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
Rabbit brain lysates; probed with LOX 1 Polyclonal Antibody, unconjugated (bs-2044R) at 1:1000 overnight at 4°C followed by a conjugated secondary antibody for 60 minutes at 37°C.
Thp-1 cells were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with LOX 1 Polyclonal Antibody(bs- 2044R)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).