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electrophoretic mobility shift assays.
Electrophoretic mobility shift assays confirmed these binding sites.
Electrophoretic mobility shift assays indicated that both Sp3 protein and Sp1protein bind to these two sites.
Dependence on Sox9 expression was confirmed by electrophoretic mobility shift assays.
Electrophoretic mobility shift assays were performed as described previously [69].
This promoter region was amplified via PCR and used in electrophoretic mobility shift assays.
Electrophoresis mobility shift assays (EMSA) were carried out as previously described [30].
Nuclear extracts were prepared, and electrophoretic mobility shift assays were performed, as previously described [5].
Electrophoretic mobility shift assays used standard methodologies that have been previously described [27], [28].
This corresponds to greater binding to NFκB probe as revealed by mobility shift assays (Fig. 5B).
Electrophoretic mobility shift assays (EMSA) were undertaken with in vitro translated Zta protein.
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