PSMD13 Antibody (PSH0-52)

Western Blot: PSMD13 Antibody (PSH0-52) [NBP3-32793]

Western Blot: PSMD13 Antibody (PSH0-52) [NBP3-32793] - Western blot analysis of PSMD13 on different lysates with Rabbit anti-PSMD13 antibody (NBP3-32793) at 1/1,000 dilution.

Lane 1: HeLa cell lysate
Lane 2: Jurkat cell lysate
Lane 3: HepG2 cell lysate
Lane 4: SiHa cell lysate
Lane 5: HEK-293 cell lysate
Lane 6: SH-SY5Y cell lysate
Lane 7: NIH/3T3 cell lysate
Lane 8: PC-12 cell lysate
Lane 9: Mouse testis tissue lysate
Lane 10: Rat testis tissue lysate

Lysates/proteins at 20 ug/Lane.

Predicted band size: 43 kDa
Observed band size: 43 kDa

Exposure time: 30 seconds;

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 (NBP3-32793) 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: PSMD13 Antibody (PSH0-52) [NBP3-32793]

Immunohistochemistry: PSMD13 Antibody (PSH0-52) [NBP3-32793] - Immunohistochemical analysis of paraffin-embedded human brain tissue with Rabbit anti-PSMD13 antibody (NBP3-32793) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (NBP3-32793) at 1/200 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: PSMD13 Antibody (PSH0-52) [NBP3-32793]

Immunocytochemistry/ Immunofluorescence: PSMD13 Antibody (PSH0-52) [NBP3-32793] - Immunocytochemistry analysis of HeLa cells labeling PSMD13 with Rabbit anti-PSMD13 antibody (NBP3-32793) at 1/200 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-PSMD13 antibody (NBP3-32793) 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. 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.