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Pitope-tagged Roc1b under the control of the Roc1b promoter were able to rescue the male sterile phenotype (Fig. 5A). Six different BNAR lines rescued the male sterility defect, five of them to the level of the control Rob1b transgenes (Fig. 5A). The BNAR chimeric proteins were expressed from the Roc1b promoter at levels comparable to normal Roc1b (Figure 5b). Because BNAR binds to Cul3, we conclu
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IDP to act as either nucleators, inhibitors, or both. It is likely that different combinations of each of the above exist in situ. IDPs in general have multiple functions. Biomineralization-related IDPs, with their flexible chains, have several possible functions, which, depending on the above-proposed mechanisms, may include [114]: (a) Stabilization of calcium phosphate nano-clusters or amorphous
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MM EDTA, 20 mM Tris-HCl, pH 8.1, 150 mM NaCl), high-salt buffer (same as the low-salt buffer but with 500 mM NaCl), LiCl buffer (0.25 M LiCl, 1 NP-40, 1 deoxycholate, 1 mM EDTA, 10 mM Tris-HCl, pH 8.1), and Tris-EDTA (pH 8.0), and then eluted with elution buffer (1 SDS, 100 mM NaHCO3). The cross-linking of protein-DNA complexes was reversed by incubation with 5 M NaCl at 65?C for 4 h, and DNA w
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MM EDTA, 20 mM Tris-HCl, pH 8.1, 150 mM NaCl), high-salt buffer (same as the low-salt buffer but with 500 mM NaCl), LiCl buffer (0.25 M LiCl, 1 NP-40, 1 deoxycholate, 1 mM EDTA, 10 mM Tris-HCl, pH 8.1), and Tris-EDTA (pH 8.0), and then eluted with elution buffer (1 SDS, 100 mM NaHCO3). The cross-linking of protein-DNA complexes was reversed by incubation with 5 M NaCl at 65?C for 4 h, and DNA w
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Ta paying particular attention to whether association with different Roc chimeras affects the steady state amount of Cullin neddylation. We could find no consistent correlation between Cullin neddylation and a particular domain of one of the Roc proteins.The Roc1b RING domain cannot provide all Roc1a functionSince the ANBR protein displays the same binding specificity as Roc1a, we wanted to determ