WB
Western blot analysis of RAP1A + RAP1B on different lysates with Rabbit anti-RAP1A + RAP1B antibody at 1/1000 dilution.
Lane 1: HeLa cell lysate,
Lane 2: Jurkat cell lysate,
Lane 3: NIH/3T3 cell lysate,
Lane 4: HEK-293 cell lysate,
Lysates/proteins at 20 µg/Lane.
Exposure time: 5 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 at 1/1000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200000 dilution was used for 1 hour at room temperature.
FC
Flow cytometric analysis of HEK-293 cells labeling RAP1A + RAP1B.
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).