Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10770859 | Biochemical and Biophysical Research Communications | 2005 | 8 Pages |
Abstract
p73, unlike p53, is expressed as a number of isomeric forms. Alternative splicing at the 3â² end of p73 transcript, together with the usage of a second promoter downstream of exon 3, can generate up to 24 p73 isoforms. Variants lacking the TA domain (ÎN isoforms) are induced by TAp73 and by p53, and inhibit their transcriptional activity. However, understanding the complex biology of p73 has been handicapped by the lack of high affinity specific antibodies for the different isoforms. Here, we report the characterization, by Western blotting and immunoprecipitation, of three new polyclonal antisera recognizing all p73 isoforms, only ÎN isoforms or only p73α, and which have advantages of affinity and specificity over previously available antibodies.
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Authors
A. Emre Sayan, Andrea Paradisi, Borek Vojtesek, Richard A. Knight, Gerry Melino, Eleonora Candi,