dUTPase Antibody (JE66-11)

Western Blot: dUTPase Antibody (JE66-11) [NBP3-32281]

Western Blot: dUTPase Antibody (JE66-11) [NBP3-32281] - Western blot analysis of dUTPase on different lysates with Rabbit anti-dUTPase antibody (NBP3-32281) at 1/1,000 dilution.

Lane 1: HeLa cell lysate (15 ug/Lane)
Lane 2: A549 cell lysate (15 ug/Lane)
Lane 3: Jurkat cell lysate (15 ug/Lane)
Lane 4: LO2 cell lysate (15 ug/Lane)
Lane 5: HepG2 cell lysate (15 ug/Lane)
Lane 6: K-562 cell lysate (15 ug/Lane)
Lane 7: HEK-293 cell lysate (15 ug/Lane)
Lane 8: A431 cell lysate (15 ug/Lane)
Lane 9: Human liver tissue lysate (30 ug/Lane)

Predicted band size: 27 kDa
Observed band size: 20 kDa

Exposure time: 3 minutes;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (NBP3-32281) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100,000 dilution was used for 1 hour at room temperature.

Immunohistochemistry: dUTPase Antibody (JE66-11) [NBP3-32281]

Immunohistochemistry: dUTPase Antibody (JE66-11) [NBP3-32281] - Immunohistochemical analysis of paraffin-embedded human esophagus tissue with Rabbit anti-dUTPase antibody (NBP3-32281) at 1/1,000 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 (NBP3-32281) at 1/1,000 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: dUTPase Antibody (JE66-11) [NBP3-32281]

Immunocytochemistry/ Immunofluorescence: dUTPase Antibody (JE66-11) [NBP3-32281] - Immunocytochemistry analysis of HCT116 cells labeling dUTPase with Rabbit anti-dUTPase antibody (NBP3-32281) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-dUTPase antibody (NBP3-32281) at 1/100 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. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (red) was stained at 1/200 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.