<p>The gene names are indicated at the bottom of each panel. They are <i>PRP1</i> (A), <i>RHS19</i> (B), <i>EXT14</i> (C), and <i>RHS15</i> (D). The experiment was performed using 0.1 μg of EIN3-GST or GST proteins. The biotin-labelled probe contained 10 fmol of the EIN3-binding element. The 500 X excess unlabeled probe (cold probe) was used as a competitor.</p
<p>(Panel A) SDS PAGE analysis of 500 ng of purified wild type and mutant GST-Czf1 fusion proteins s...
<p>(A) qRT-PCR analysis of <i>POD</i>s expression. (B) Measurement of POD activity. The treated seed...
<p>(A) Description of oligonucleotide probes of wild-type (WT) (-22 to +8) and mutant (MT) RIG-I IRF...
<p>(A) Reported natural promoters of EIN3 targets. EBSs are shown in red. The spacing sequences betw...
<p>Analysis by EMSA of the binding of GST-PimR<sup>SARP</sup> to the <i>pimR-M</i> promoter region. ...
A. Direct EMSA with the following probes: tamA, pckA, bvrR, omp25, virB1, and negative controls rplL...
(A) Labeled WT and Mut oligos of the second binding site (+113/+122) on the 5’ UTR are shown in lane...
<p>Upper panel represents schematic illustration of putative GLI binding sites. Positions relative t...
<p>(A) EMSA was performed by using biotinylated <i>ckβ</i>-Ets/GATA probes with or without mutations...
<p>(<b>A</b>) Nuclear extracts from SW480, HCT-116, and RKO cell lines were incubated with IR-dye la...
<p>Wt proximal γ-globin promoter probe with nuclear extracts from human fetal liver, K562 cells and ...
<p>All samples contained binding buffer (1.5 µL), Poly dI:dC (1.5 µL), G allele or A allele probe (0...
<p>(A) Sequences of the oligonucleotides used as probes in EMSA assays. Each FOXP3 binding site is u...
<p><b>A.</b> 5′-end biotin-labeled double-stranded oligonucleotides probes including −462 G (lane 1–...
<p>(<b>A</b>) Electrophoretic gel mobility shift assays (EMSAs) of the mouse <i>Csn3</i> DR5 RARE. E...
<p>(Panel A) SDS PAGE analysis of 500 ng of purified wild type and mutant GST-Czf1 fusion proteins s...
<p>(A) qRT-PCR analysis of <i>POD</i>s expression. (B) Measurement of POD activity. The treated seed...
<p>(A) Description of oligonucleotide probes of wild-type (WT) (-22 to +8) and mutant (MT) RIG-I IRF...
<p>(A) Reported natural promoters of EIN3 targets. EBSs are shown in red. The spacing sequences betw...
<p>Analysis by EMSA of the binding of GST-PimR<sup>SARP</sup> to the <i>pimR-M</i> promoter region. ...
A. Direct EMSA with the following probes: tamA, pckA, bvrR, omp25, virB1, and negative controls rplL...
(A) Labeled WT and Mut oligos of the second binding site (+113/+122) on the 5’ UTR are shown in lane...
<p>Upper panel represents schematic illustration of putative GLI binding sites. Positions relative t...
<p>(A) EMSA was performed by using biotinylated <i>ckβ</i>-Ets/GATA probes with or without mutations...
<p>(<b>A</b>) Nuclear extracts from SW480, HCT-116, and RKO cell lines were incubated with IR-dye la...
<p>Wt proximal γ-globin promoter probe with nuclear extracts from human fetal liver, K562 cells and ...
<p>All samples contained binding buffer (1.5 µL), Poly dI:dC (1.5 µL), G allele or A allele probe (0...
<p>(A) Sequences of the oligonucleotides used as probes in EMSA assays. Each FOXP3 binding site is u...
<p><b>A.</b> 5′-end biotin-labeled double-stranded oligonucleotides probes including −462 G (lane 1–...
<p>(<b>A</b>) Electrophoretic gel mobility shift assays (EMSAs) of the mouse <i>Csn3</i> DR5 RARE. E...
<p>(Panel A) SDS PAGE analysis of 500 ng of purified wild type and mutant GST-Czf1 fusion proteins s...
<p>(A) qRT-PCR analysis of <i>POD</i>s expression. (B) Measurement of POD activity. The treated seed...
<p>(A) Description of oligonucleotide probes of wild-type (WT) (-22 to +8) and mutant (MT) RIG-I IRF...