Bromodeoxyuridine/BrdU Antibody (A9C7-R)

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (A9C7-R) [NBP3-32092]

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (A9C7-R) [NBP3-32092] - Immunofluorescence analysis of paraffin-embedded Bromodeoxyuridine/BrdU treated mouse embryo tissue labeling BrdU with Mouse anti-Bromodeoxyuridine/BrdU antibody (NBP3-32092) at 1/500 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (NBP3-32092, green) at 1/500 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Mouse 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 (A9C7-R) [NBP3-32092]

Immunohistochemistry: Bromodeoxyuridine/BrdU Antibody (A9C7-R) [NBP3-32092] - Immunohistochemical analysis of paraffin-embedded Bromodeoxyuridine/BrdU treated mouse embryo tissue with Mouse anti-Bromodeoxyuridine/BrdU antibody (NBP3-32092) at 1/5,000 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 (NBP3-32092) at 1/5,000 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 (A9C7-R) [NBP3-32092]

Immunocytochemistry/ Immunofluorescence: Bromodeoxyuridine/BrdU Antibody (A9C7-R) [NBP3-32092] - Immunocytochemistry analysis of Bromodeoxyuridine/BrdU treated NIH/3T3 cells labeling Bromodeoxyuridine/BrdU with Mouse anti-Bromodeoxyuridine/BrdU antibody (NBP3-32092) at 1/250 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Mouse anti-Bromodeoxyuridine/BrdU antibody (NBP3-32092) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Mouse 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.

beta Tubulin (red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Rabbit IgG H&L (iFluor™ 594) were used as the secondary antibody at 1/1,000 dilution.