WB
Western blot analysis of lysates from wild type (WT) and 293T cells transfected with CD62E using CD62E Rabbit mAb at 1:1000 dilution incubated overnight at 4℃. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 20 μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit.Exposure time: 30s.
ICC/IF
Confocal imaging of 293T cells transfected with CD62E using CD62E Rabbit mAb (dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.
FC
Flow cytometry: 1X10^6 CHO cells (negative control,left) and CHO (Transfection,right) cells were surface-stained with CD62E Rabbit mAb (2 μg/mL,orange line) or Rabbit IgG isotype control (2 μg/mL,blue line), followed by PE Goat anti-Rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
FC
Flow cytometry: 1X10^6 CHO (Transfection) cells were surface-stained with Rabbit IgG isotype control (2 μg/mL,left) or CD62E Rabbit mAb (2 μg/mL,right), followed by PE Goat anti-Rabbit pAb staining.