Figure 2.
Figure 2. Detection of binding proteins to the TME by EMSA. (A) Sense sequences of the double-stranded oligonucleotides used in EMSA. TME indicates the wild-type TME sequence. Mutant oligonucleotides, Mut-1 to Mut-7, have various mutations in the TME and were used as the competitors. Bold underlined text indicates mutated sequences. (B) Wild-type TME EMSA performed with 6 μg nuclear extracts from 4 cell lines. (C-D) Competition experiments performed with nuclear extracts from HEL (C) and HepG2 (D) cells. (–) indicates no competitor. Arrows indicate the specific competed bands.

Detection of binding proteins to the TME by EMSA. (A) Sense sequences of the double-stranded oligonucleotides used in EMSA. TME indicates the wild-type TME sequence. Mutant oligonucleotides, Mut-1 to Mut-7, have various mutations in the TME and were used as the competitors. Bold underlined text indicates mutated sequences. (B) Wild-type TME EMSA performed with 6 μg nuclear extracts from 4 cell lines. (C-D) Competition experiments performed with nuclear extracts from HEL (C) and HepG2 (D) cells. (–) indicates no competitor. Arrows indicate the specific competed bands.

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