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. 2009 Jan 30;284(5):3125–3135. doi: 10.1074/jbc.M807466200

TABLE 2.

Oligonucleotides for electrophoretic mobility shift assays Wild type and mutant oligonucleotides were used in gel shift assays. The YR oligonucleotide containing one Y-repeat region (underlined) from the Runx2 P1 promoter was used as the probe for the electrophoretic mobility shift assay. Other oligonucleotides were used as competitors. Sp1-con, Sp1 consensus binding sites; Ets1-con, Ets1 consensus binding sites; Sp1-Mut, Sp1 consensus with mutations (lowercase) in the Sp1 element; Ets1-Mut, Ets1 consensus with mutations (lowercase) in the Ets1 element.

Oligonucleotide Sequence (5′–3′)
YR CAGAAGAGAAAGAGGGAGGGGAGGGGAG
YR-M1 CAGAAacaAAAGAGGGAGGGGAGGGGAG
YR-M2 CAGAAGAGAAAGAGtfAGGGGAGGGGAG
YR-M3 CAGAAGAGAAAGAGGGAGGttAGGGGAG
Sp1-con ATTCGATCGGGGCGGGGCGAGC
Sp1-Mut ATTCGATCGGttCGGGGCGAGC
Ets1-con GATCTCGAGCAGGAAGTTCGA
Ets1-Mut GATCTCGAGCAaGAAGTTCGA