<p>The Alba proteins with the His-tag are marked as A1-h and A2-h and without the His-tag as A1 and A2. Lane 1: linear DNA (pUC19/<i>Eco</i>RI) in the absence of the Alba proteins. Lanes 2–5: DNA with and without the His-tagged Alba proteins, as indicated.</p
<p>The binding of wild type H-NST and mutant H-NST to <i>LEE</i> DNA targets was determined by elect...
Transcription factors lie at the center of gene regulation, and their identification is crucial to t...
<p>(a) Lane 1, <sup>32</sup>P-labeled MSgt-FSgt probe only; lane 2–3, <sup>32</sup>P-labeled MSgt-FS...
<p>Electrophoresis mobility shift assay using the purified CBS domain protein (CBSDP) and a 309 bp D...
<p>For each PBS, the DNA (10 mM) was incubated with increasing concentrations (0, 1nM, 1.7nM and 2.3...
<p>Different nucleic acid substrates (full length tRNA, 17 nucleotide anticodon stem-loop and DNA) w...
Higher electrophoretic mobility band of pUC19 (hmP19) DNA is not double-stranded in nature. pUC19 pl...
<p>(<b>A</b>) A positive result (band shift) was observed with all the tested FA genes. Lane 1: cont...
<p>A. Electrophoretic mobility shift assay of labeled TAL868 target DNA with T, A, C, or G in the 0<...
Background: Architectural proteins have important roles in compacting and organising chromosomal DNA...
<p>Cell lysate from Gli3RD or mock-transfected HEK293 cells incubated with labelled scrambled sequen...
BACKGROUND: Architectural proteins have important roles in compacting and organising chromosomal DNA...
<p><b>(A)</b> Electrophoretic mobility shift assay (EMSA) for AP-1 binding in nuclear extracts (NEs)...
<p><b>(A)</b> Result of EMSA with the wild type Stl protein. Note that the DNA band is shifted upwar...
<p>Binding reaction was performed with a labeled 200 bp DNA fragment encompassing the <i>mecA</i> pr...
<p>The binding of wild type H-NST and mutant H-NST to <i>LEE</i> DNA targets was determined by elect...
Transcription factors lie at the center of gene regulation, and their identification is crucial to t...
<p>(a) Lane 1, <sup>32</sup>P-labeled MSgt-FSgt probe only; lane 2–3, <sup>32</sup>P-labeled MSgt-FS...
<p>Electrophoresis mobility shift assay using the purified CBS domain protein (CBSDP) and a 309 bp D...
<p>For each PBS, the DNA (10 mM) was incubated with increasing concentrations (0, 1nM, 1.7nM and 2.3...
<p>Different nucleic acid substrates (full length tRNA, 17 nucleotide anticodon stem-loop and DNA) w...
Higher electrophoretic mobility band of pUC19 (hmP19) DNA is not double-stranded in nature. pUC19 pl...
<p>(<b>A</b>) A positive result (band shift) was observed with all the tested FA genes. Lane 1: cont...
<p>A. Electrophoretic mobility shift assay of labeled TAL868 target DNA with T, A, C, or G in the 0<...
Background: Architectural proteins have important roles in compacting and organising chromosomal DNA...
<p>Cell lysate from Gli3RD or mock-transfected HEK293 cells incubated with labelled scrambled sequen...
BACKGROUND: Architectural proteins have important roles in compacting and organising chromosomal DNA...
<p><b>(A)</b> Electrophoretic mobility shift assay (EMSA) for AP-1 binding in nuclear extracts (NEs)...
<p><b>(A)</b> Result of EMSA with the wild type Stl protein. Note that the DNA band is shifted upwar...
<p>Binding reaction was performed with a labeled 200 bp DNA fragment encompassing the <i>mecA</i> pr...
<p>The binding of wild type H-NST and mutant H-NST to <i>LEE</i> DNA targets was determined by elect...
Transcription factors lie at the center of gene regulation, and their identification is crucial to t...
<p>(a) Lane 1, <sup>32</sup>P-labeled MSgt-FSgt probe only; lane 2–3, <sup>32</sup>P-labeled MSgt-FS...