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. 2009 Sep 11;285(7):4757–4770. doi: 10.1074/jbc.M109.056200

FIGURE 1.

FIGURE 1.

Proteins used in this study separated on 9% Laemmli-Tricine SDS gels (7). A, shown is an autoradiograph of the in vitro transcription/translation product of full-length (77 kDa) protein 4.2, labeled with [35S]methionine. B, shown is the cytoplasmic domain of band 3 cleaved and purified from red cell membranes stripped of peripheral proteins (17). C, shown are recombinant proteins used in this study. 8 μg of each protein were analyzed. In some cases (lanes 3, 4, and 9) the GST moiety had been cleaved from the recombinant fusion proteins with PreScission protease (Amersham Biosciences) before electrophoresis.