Bromodeoxyuridine/BrdU Antibody (PSH0-18)

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (PSH0-18) [NBP3-32093]

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (PSH0-18) [NBP3-32093] - Immunofluorescence analysis of paraffin-embedded Bromodeoxyuridine/BrdU treated mouse embryo tissue labeling BrdU with Rabbit anti-Bromodeoxyuridine/BrdU antibody (NBP3-32093) at 1/2,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32093, green) at 1/2,000 dilution overnight at 4 ℃, washed with PBS.

Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (PSH0-18) [NBP3-32093]

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (PSH0-18) [NBP3-32093] - Immunohistochemical analysis of paraffin-embedded Brdu treated / Untreated / Edu treated mouse embryo brain tissue with Rabbit anti-Bromodeoxyuridine/BrdU antibody (NBP3-32093) at 1/10,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (NBP3-32093) at 1/10,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Immunocytochemistry/ Immunofluorescence: Bromodeoxyuridine/BrdU Antibody (PSH0-18) [NBP3-32093]

Immunocytochemistry/ Immunofluorescence: Bromodeoxyuridine/BrdU Antibody (PSH0-18) [NBP3-32093] - Immunocytochemistry analysis of NIH/3T3 cells (Untreated / Brdu treated / Edu treated) labeling Bromodeoxyuridine/BrdU with Rabbit anti-Bromodeoxyuridine/BrdU antibody (NBP3-32093) at 1/200 dilution.

Cells were fixed in 70% ethyl alcohol for 5 minutes at room temperature, then subjected to acid hydrolysis using 2M HCL in TBST for 30 minutes at room temperature. permeabilized with 0.1% Triton X-100 in PBS for 15 minutes, and then blocked with 2% BSA for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-Bromodeoxyuridine/BrdU antibody (NBP3-32093) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.