Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)
Western blot analysis of various lysates using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555) at 1:1000 dilution incubated overnight at 4℃. 293T and C6 cells were treated by UV at room temperature for 15-30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 20s.
Western blot - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)
Western blot analysis of lysates from NIH/3T3 cells using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555) at 1:1000 dilution incubated overnight at 4℃. NIH/3T3 cells were treated by UV at room temperature for 15-30 minutes.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3 % nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 45s.
Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)
Confocal imaging of 293T cells (treated with UV) and 293T cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). Objective: 100x.
Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)
Confocal imaging of NIH/3T3 cells (treated with UV) and NIH/3T3 cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
Immunofluorescence - Phospho-Histone H2AX-S139 Rabbit mAb (AP1555)
Confocal imaging of C6 cells (treated with UV) and C6 cells (untreated) using Phospho-Histone H2AX-S139 Rabbit mAb (AP1555, dilution 1:2000) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.