BDNF Polyclonal Antibody

U251 cells; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum) at 37C for 20 min; Antibody incubation with BDNF Polyclonal Antibody, Unconjugated (bs-4989R) 1:200, 90 minutes at 37C; followed by a conjugated secondary antibody (bs-0295G-FITC) at 37C for 90 minutes, DAPI (5ug\/ml) was used to stain the cell nuclei.

Paraformaldehyde-fixed, paraffin embedded mouse brain; Antigen retrieval by boiling in sodium citrate buffer (pH6) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 30 minutes; Blocking buffer (normal goat serum) at 37\u00b0C for 20min; Antibody incubation with BDNF Polyclonal Antibody (bs-4989R) at 1:400 overnight at 4\u00b0C, followed by a conjugated secondary and DAB staining.

HepG2 cells were fixed with 4% PFA for 10min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with BDNF Polyclonal Antibody(bs-4989R) 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 incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), no antibody control control (blue), secondary antibody only (light blue) and isotype control (orange).

Lane 1: Mouse Cerebrum cell lysates probed with BDNF Polyclonal Antibody, Unconjugated (bs-4989R) at 1:300 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.

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\u00b0C for 30min; Antibody incubation with BDNF Polyclonal Antibody, Unconjugated (bs-4989R) at 1:400 overnight at 4\u00b0C, DAB staining.

Paraformaldehyde-fixed, paraffin embedded (rat cerebellum); 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\u00b0C for 30min; Antibody incubation with (BDNF) Polyclonal Antibody, Unconjugated (bs-4989R) at 1:200 overnight at 4\u00b0C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.