ALDH2 Antibody (7-D8-R)

Western Blot: ALDH2 Antibody (7-D8-R) [NBP3-32022]

Western Blot: ALDH2 Antibody (7-D8-R) [NBP3-32022] - Western blot analysis of ALDH2 on different lysates with Mouse anti-ALDH2 antibody (NBP3-32022) at 1/1,000 dilution.

Lane 1: 293T cell lysate (20 ug/Lane)
Lane 2: HepG2 cell lysate (20 ug/Lane)
Lane 3: K-562 cell lysate (20 ug/Lane)
Lane 4: A549 cell lysate (20 ug/Lane)
Lane 5: THP-1 cell lysate (20 ug/Lane)
Lane 6: Human liver tissue lysate (40 ug/Lane)
Lane 7: Rat liver tissue lysate (40 ug/Lane)
Lane 8: Rat testis tissue lysate (40 ug/Lane)

Predicted band size: 56 kDa
Observed band size: 54 kDa

Exposure time: 1 minute 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 (NBP3-32022) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.

Immunohistochemistry: ALDH2 Antibody (7-D8-R) [NBP3-32022]

Immunohistochemistry: ALDH2 Antibody (7-D8-R) [NBP3-32022] - Immunohistochemical analysis of paraffin-embedded human liver tissue with Mouse anti-ALDH2 antibody (NBP3-32022) at 1/2,000 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 (NBP3-32022) at 1/2,000 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: ALDH2 Antibody (7-D8-R) [NBP3-32022]

Immunocytochemistry/ Immunofluorescence: ALDH2 Antibody (7-D8-R) [NBP3-32022] - Immunocytochemistry analysis of HepG2 cells labeling ALDH2 with Mouse anti-ALDH2 antibody (NBP3-32022) at 1/100 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-ALDH2 antibody (NBP3-32022) at 1/100 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.