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Fig. 4. Forms of Ngn3 lacking lysines are stabilised by Mg132.Degradation assays at a fixed point of 90 minutes were performed in interphase (A) and mitotic (B) Xenopus egg extract using 35S-IVT Ngn3 and mutants thereof, as labelled, in either the presence or absence of 100 µM Mg132 proteasome inhibitor. Samples were run on SDS-PAGE gels, analysed by autoradiography (A,B).

Image published in: Roark R et al. (2012)

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