WB
Western blot analysis of various lysates using p70 S6 Kinase 1 Rabbit mAb at 1:1000 dilutionincubated overnight at 4℃.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 30s.
ICC/IF
Confocal imaging of 293T cells using p70 S6Kinase 1 Rabbit mAb (dilution 1:200)followed by a further incubation with Cy3Goat Anti-Rabbit IgG (H+L) (dilution1:500) (Red). DAPI was used for nuclearstaining (Blue). Objective: 100x.
ICC/IF
Confocal imaging of NIH/3T3 cells using p70S6 Kinase 1 Rabbit mAb (dilution1:200) followed by a further incubation withCy3 Goat Anti-Rabbit IgG (H+L) (dilution 1:500) (Red). The cells werecounterstained with α-Tubulin Mouse mAb(dilution 1:400) followed byincubation with ABflo® 488-conjugated GoatAnti-Mouse IgG (H+L) Ab (dilution1:500) (Green). DAPI was used for nuclearstaining (Blue). Objective: 100x.
ICC/IF
Confocal imaging of C6 cells using p70 S6Kinase 1 Rabbit mAb (dilution 1:200)followed by a further incubation with Cy3Goat Anti-Rabbit IgG (H+L) (dilution1:500) (Red). The cells were counterstainedwith α-Tubulin Mouse mAb (dilution1:400) followed by incubation with ABflo®488-conjugated Goat Anti-Mouse IgG (H+L)Ab (dilution 1:500) (Green). DAPI wasused for nuclear staining (Blue). Objective:100x.