WB
Western blot analysis of lysates from NIH/3T3 cells using Phospho-Histone H2AX-S139 Rabbit pAb at 1:400 dilution. NIH/3T3 cells were treated with UV at room temperature for 15-30 minutes.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit.Exposure time: 20s.
WB
Western blot analysis of lysates from C6 cells using Phospho-Histone H2AX-S139 Rabbit pAb at 1:400 dilution. C6 cells were treated with UV at room temperature for 15-30 minutes.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 20s.
IF
Immunofluorescence analysisof 293T(treated with UV) and293T(untreated) cells using Phospho-HistoneH2AX-S139 Rabbit pAb at a dilutionof 1:100 (40x lens). Secondary antibody:Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI fornuclear staining.
IHC
Immunohistochemistry analysis of paraffinembedded Human liver tissueusing Phospho-Histone H2AX-S139 RabbitpAb at a dilution of 1:100 (40xlens). High pressure antigen retrieval wasperformed with 0.01 M citrate buffer (pH 6.0)prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffinembedded Rat lung tissue using PhosphoHistone H2AX-S139 Rabbit pAb at adilution of 1:100 (40x lens). High pressureantigen retrieval was performed with 0.01 Mcitrate buffer (pH 6.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffinembedded Mouse heart tissueusing Phospho-Histone H2AX-S139 RabbitpAb at a dilution of 1:100 (40xlens). High pressure antigen retrieval wasperformed with 0.01 M citrate buffer (pH 6.0)prior to IHC staining.