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Evaluation of p63 and p73 antibodies for cross-reactivity.
- Source :
-
Cell cycle (Georgetown, Tex.) [Cell Cycle] 2009 Nov 15; Vol. 8 (22), pp. 3702-6. Date of Electronic Publication: 2009 Nov 09. - Publication Year :
- 2009
-
Abstract
- The tumor suppressor p53 is commonly mutated in human cancers. However, two homologs of p53, p63 and p73, are frequently overexpressed in tumors and are associated with tumor subtypes, clinical outcomes, and responses to therapy. There are many isoforms of p53, p63 and p73 (the p53 family). Proper detection of and discrimination between the members of this tumor suppressor family in human tissues is of critical importance to cancer research and clinical care. In this study, we assessed the specificity of several commercially available and newly generated p73 antibodies, focusing on antibodies that distinguish between the TA p73 and DeltaNp73 isoforms by western analysis, immunohistochemistry, and immunofluorescence. In addition, we found that the pan-p63 and pan-p73 antibodies tested cross-react with p73 and p63 respectively. The results of this study have important implications for analysis of p63 and p73 expression and co-expression in human tumors, and for potential use of these reagents in molecular diagnostics and therapeutic decision-making.
- Subjects :
- Blotting, Western
Cell Line, Tumor
DNA-Binding Proteins immunology
Fluorescent Antibody Technique
Humans
Immunohistochemistry
Nuclear Proteins immunology
Trans-Activators immunology
Transcription Factors
Tumor Protein p73
Tumor Suppressor Proteins immunology
Antibodies metabolism
Antibody Specificity immunology
Cross Reactions immunology
DNA-Binding Proteins metabolism
Neoplasms metabolism
Nuclear Proteins metabolism
Trans-Activators metabolism
Tumor Suppressor Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1551-4005
- Volume :
- 8
- Issue :
- 22
- Database :
- MEDLINE
- Journal :
- Cell cycle (Georgetown, Tex.)
- Publication Type :
- Academic Journal
- Accession number :
- 19855172
- Full Text :
- https://doi.org/10.4161/cc.8.22.10036