Cytochrome P450 1A2 Antibody (JE39-22)

Western Blot: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241]

Western Blot: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Western blot analysis of Cytochrome P450 1A2 on HepG2 cell lysates with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/1,000 dilution.

Lysates/proteins at 10 ug/Lane.

Predicted band size: 58 kDa
Observed band size: 50 kDa

Exposure time: 2 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 (NBP3-32241) 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.

Immunocytochemistry/ Immunofluorescence: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241]

Immunocytochemistry/ Immunofluorescence: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Immunocytochemistry analysis of HepG2 cells labeling Cytochrome P450 1A2 with Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) 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 Rabbit anti-Cytochrome P450 1A2 antibody (NBP3-32241) at 1/250 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit 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-Mouse IgG H&L (iFluor™ 594) was used as the secondary antibody at 1/1,000 dilution.

Flow Cytometry: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241]

Flow Cytometry: Cytochrome P450 1A2 Antibody (JE39-22) [NBP3-32241] - Flow cytometric analysis of HepG2 cells labeling Cytochrome P450 1A2.

Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32241, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).