Table 1.
Sequences of primers and oligonucleotides used for generation of constructs, mutagenesis, and EMSA probes.
| Primer/oligonucleotide | Sequence (5′ → 3′) |
|---|---|
| −1432F | GGGGTACCCAAAGGTTCTCCCACGGTTC |
| −906F | GGGGTACCACTGCTGATACAGCTCTCCT |
| −472F | GGGGTACCTCCCTCAGACTCAGGAGTGC |
| −99F | GGGGTACCAGGTTCCTGCCAAGTGTGTCA |
| −63F | GGGGTACCGGAGTGGGGAGGGCACGT |
| −20F | GGGGTACCTGGTATTTCTGCGTTCACCAG |
| CR | GGAAGATCTTGGGGCTCAGGCAAAGTGAA |
| mSp1-A F | TACCGGAGTGGttgaGGCACGTGGGCGGGCCT |
| mSp1-A R | AGGCCCGCCCACGTGCCtcaaCCACTCCGGTA |
| mSp1-B F | AGGGCACGTGttgaGGCCTGTCTG |
| mSp1-B R | CAGACAGGCCtcaaCACGTGCCCT |
| FGF21-probe | GCACGTGGGCGGGCCTGTCTG |
| Sp1C-probe | GTCAAGTTCGGGGAGGGGGATCAG |
Kpn I and Bgl II restriction sites are underlined. CR, common reverse primer.
Substitution mutations are represented in lowercase letters.