epitope mapping near the C-terminus of Daxx of mouse origin
recommended for detection of Daxx of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA; also reactive with additional species, including equine, canine, bovine and porcine
Daxx Background Information Activation of the cell surface receptor FAS by FAS ligand leads to the initiation of apoptosis, a process necessary for the regulation of the immune system and tissue homeostasis. FAS-mediated apoptosis appears to involve a number of divergent and overlapping pathways. Daxx appears to be a central component of a FAS-mediated apoptotic pathway involving the activation of Jun N-terminal kinase (JNK). Although Daxx itself does not contain a death domain, it specifically binds to the death domain of FAS. Overexpression of Daxx activates the JNK pathway and enhances FAS-mediated apoptosis. The Daxx apoptotic pathway acts cooperatively with but is distinct from the FAS-mediated pathway that involves interactions between the death domain-containing protein FADD and the cysteine protease FLICE. Unlike the FAS-FADD-FLICE pathway, the Daxx pathway is sensitive to the apoptotic inhibitor protein Bcl-2.
Daxx (S-20) Product Citations
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Daxx (S-20)
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Daxx (S-20): sc-7001. Western blot analysis of Daxx expression in MOLT-4 (A) and Ramos (B) whole cell lysates.
Daxx (S-20): sc-7001. Immunoperoxidase staining of formalin-fixed, paraffin-embedded human breast tumor showing cytoplasmic localization.