IHC image of ab26802 staining in human breast adenocarcinoma formalin fixed paraffin embedded tissue section, performed on a Leica BondTM 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 ab26802, 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 - Anti-PUMA antibody (ab26802)
Anti-PUMA antibody (ab26802) at 2 µg/ml + MEF1 (Mouse embryonic fibroblast cell line) Whole Cell Lysate at 20 µg
Secondary Goat Anti-Rabbit IgG H&L (HRP) preadsorbed (ab97080) at 1/5000 dilution Developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 20 kDa Observed band size : 20 kDa Additional bands at : 40 kDa,58 kDa. We are unsure as to the identity of these extra bands.
Exposure time : 20 minutes
Anti-PUMA antibody (ab26802) 使用論文
has not yet been referenced specifically in any publications.