VALIDATION IMAGES
Mouse splenocytes probed with Rabbit Anti-CX3CR1 Polyclonal Antibody, FITC Conjugated (bs-1728R-FITC) (green) at 1:100 for 40 minutes compared to control cells (blue).\n
Lane 1: rat brain lysates Lane 2: mouse heart lysates probed with Anti CX3CR1 Polyclonal Antibody, Unconjugated (bs-1728R) at 1:200 in 4˚C. Followed by conjugation to secondary antibody (bs-0295G-HRP) at 1:3000 90min in RT. Predicted band 39kD. Observed band size: 39kD.
Lane 1: Mouse Heart lysates; Lane 2: Rat Heart lysates probed with CX3CR1 Polyclonal Antibody, Unconjugated (bs-1728R) 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: Mouse Lymph node lysates; Lane 2: Mouse Lung lysates; Lane 3: Mouse Cerebrum lysates; Lane 4: Mouse Spleen cell lysates probed with CX3CR1 Polyclonal Antibody, Unconjugated (bs-1728R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.
Raw264.7 cells were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with CX3CR1 Polyclonal Antibody(bs-1728R)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).
Paraformaldehyde-fixed, paraffin embedded (rat spinal cord); 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 (CX3CR1) Polyclonal Antibody, Unconjugated (bs-1728R) at 1:1000 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Lane 1: Mouse Spinal cord tissue lysates; Lane 2: Mouse Cerebrum tissue lysates; Lane 3: Rat Spinal cord tissue lysates; Lane 4: Rat Cerebrum tissue lysates probed with CX3CR1 Polyclonal Antibody, Unconjugated (bs-1728R) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.