The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide was removed by chromatography using non-phosphopeptide corresponding to the phosphorylation site.
IHC image of SSB (phospho S366) staining in Human breast adenocarcinoma formalin fixed paraffin embedded tissue section, performed on a Leica Bond™ system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab61800, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
Western blot - SSB (phospho S366) antibody (ab61800)
All lanes : Anti-SSB (phospho S366) antibody (ab61800) at 1/500 dilution
Lane 1 : extracts from 293 cells Lane 2 : extracts from 293 cells with immunizing peptide
Lysates/proteins at 5 µg per lane.
Predicted band size: 45 kDa Observed band size: 45 kDa