WDR41 Antibody (A9C10)

Western Blot: WDR41 Antibody (A9C10) [NBP3-33100]

Western Blot: WDR41 Antibody (A9C10) [NBP3-33100] - Western blot analysis of WDR41 on different lysates with Mouse anti-WDR41 antibody (NBP3-33100) at 1/1,000 dilution.

Lane 1: Daudi cell lysate
Lane 2: SiHa cell lysate

Lysates/proteins at 10 ug/Lane.

Predicted band size: 52 kDa
Observed band size: 52 kDa

Exposure time: 2 minutes;

10% 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 (NBP3-33100) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1:150,000 dilution was used for 1 hour at room temperature.

Immunohistochemistry: WDR41 Antibody (A9C10) [NBP3-33100]

Immunohistochemistry: WDR41 Antibody (A9C10) [NBP3-33100] - Immunohistochemical analysis of paraffin-embedded rat kidney tissue with Mouse anti-WDR41 antibody (NBP3-33100) at 1/1,000 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 (NBP3-33100) 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: WDR41 Antibody (A9C10) [NBP3-33100]

Immunocytochemistry/ Immunofluorescence: WDR41 Antibody (A9C10) [NBP3-33100] - Immunocytochemistry analysis of Hela cells labeling WDR41 with Mouse anti-WDR41 antibody (NBP3-33100) at 1/200 dilution.

Cells were fixed in 4% paraformaldehyde for 30 minutes, 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 Mouse anti-WDR41 antibody (NBP3-33100) at 1/200 dilution in 2% BSA 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.