WB
Western blot analysis of ESE1 on different lysates with Rabbit anti-ESE1 antibody at 1/1000 dilution.
Lane 1: A549 cell lysate (10 µg/Lane),
Lane 2: SK-Br-3 cell lysate (10 µg/Lane),
Lane 3: A431 cell lysate (10 µg/Lane),
Lane 4: Mouse lung tissue lysate (20 µg/Lane),
Lane 5: Rat kidney tissue lysate (20 µg/Lane),
Exposure time: 40 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 at 1/1000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:100000 dilution was used for 1 hour at room temperature.
FC
Flow cytometric analysis of A431 cells labeling ESE1.
Cells were fixed and permeabilized. Then stained with the primary antibody (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 1/1000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).