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The Myc tag monoclonal antibody 9E10 displays highly variable epitope recognition dependent on neighboring sequence context.

Science signaling (2020-01-30)
Stefan Schüchner, Christian Behm, Ingrid Mudrak, Egon Ogris
RESUMEN

Epitope tags are short, linear antibody recognition sequences that enable detection of tagged fusion proteins by antibodies. Epitope tag position and neighboring sequences potentially affect its recognition by antibodies, and such context-dependent differences in tag binding may have a wide-ranging effect on data interpretation. We tested by Western blotting six antibodies that recognize the c-Myc epitope tag, including monoclonal antibodies 9E10, 4A6, 9B11, and 71D10 and polyclonal antibodies 9106 and A-14. All displayed context-dependent differences in their ability to detect N- or C-terminal Myc-tagged proteins. In particular, clone 9E10, the most cited Myc-tag antibody, displayed high context-dependent detection variability, whereas others, notably 4A6 and 9B11, showed much less context sensitivity in their detection of Myc-tagged proteins. The very high context sensitivity of 9E10 was further substantiated by peptide microarray analyses. We conclude that recently developed, purpose-made monoclonal antibodies specific for Myc have much more uniform reactivity in diverse assays and are much less context sensitive than is the legacy antibody 9E10.

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Sigma-Aldrich
Anticuerpo anti-c-Myc, monoclonal de ratón antibody produced in mouse, clone 9E10, purified from hybridoma cell culture
Sigma-Aldrich
Anticuerpo anti-etiqueta Myc, clon 4A6, clone 4A6, Upstate®, from mouse
Sigma-Aldrich
Anti-PP2A Antibody, A subunit, Upstate®, from rabbit