<p>Chromatin from SH-SY5Y was prepared at 72 hours after treatment with 5 µM DAC and precipitated with antibodies directed against IgG, Sp1 and RNA pol II. After DNA recovery, the precipitates were evaluated by real-time PCR as described in Experimental Procedures. Results are expressed as fold change over IgG and represent means of at least three independent experiments ± SEM (* p<0.001).</p
<p>A. HeLa cells were synchronized by nocodazole for 16 h before mitotic cells were separated from a...
<p>Exponentially growing cells were treated with 0.1 mg/ml CHX at 25°C. (A) Cellular amounts of Pol2...
<p>Cells were treated with or without LPS for 1 h. ChIP assays were carried out using an anti-p65 an...
<p>(A, C, E, G) The locations of primers used in this assay are shown under the gene structures. (B,...
<p>Cells were either untreated or treated with 1 µM of JQ1 for 2 hours. (A) Pol II was detected by a...
overnight with 5 g of anti-MSH2 antibodies, purified IgG, or poly-clonal anti-acetyl-histone H4 anti...
<p>(A) Schematic representation of the HCMV genes and host GAPDH gene examined by chromatin immunopr...
17. Chromatin immunoprecipitations were performed es-sentially as described (7, 8). Fission yeast ce...
<p>Chromatin proteins and DNA in THP1 cells were cross-linked in 1% formaldehyde for 10 minutes. Cel...
<p>Conventional RT-PCR analysis, using primers hybridizing to the 5′ region, was used for detection ...
Chromatin-immunoprecipitation (ChIP) employs generally a mild formaldehyde cross-linking step, which...
<p>BM cells from 3 mice (A–B) and two healthy human donors (C–D) were extracted and fixed in formald...
<p>Ba/F3 cells were pre-treated 30 minutes with 0.2 µM TSA or 10 µM α-Br-TMC before being stimulated...
Chromatin-immunoprecipitation (ChIP) employs generally a mild formaldehyde cross-linking step, which...
<div><p>Chromatin-immunoprecipitation (ChIP) employs generally a mild formaldehyde cross-linking ste...
<p>A. HeLa cells were synchronized by nocodazole for 16 h before mitotic cells were separated from a...
<p>Exponentially growing cells were treated with 0.1 mg/ml CHX at 25°C. (A) Cellular amounts of Pol2...
<p>Cells were treated with or without LPS for 1 h. ChIP assays were carried out using an anti-p65 an...
<p>(A, C, E, G) The locations of primers used in this assay are shown under the gene structures. (B,...
<p>Cells were either untreated or treated with 1 µM of JQ1 for 2 hours. (A) Pol II was detected by a...
overnight with 5 g of anti-MSH2 antibodies, purified IgG, or poly-clonal anti-acetyl-histone H4 anti...
<p>(A) Schematic representation of the HCMV genes and host GAPDH gene examined by chromatin immunopr...
17. Chromatin immunoprecipitations were performed es-sentially as described (7, 8). Fission yeast ce...
<p>Chromatin proteins and DNA in THP1 cells were cross-linked in 1% formaldehyde for 10 minutes. Cel...
<p>Conventional RT-PCR analysis, using primers hybridizing to the 5′ region, was used for detection ...
Chromatin-immunoprecipitation (ChIP) employs generally a mild formaldehyde cross-linking step, which...
<p>BM cells from 3 mice (A–B) and two healthy human donors (C–D) were extracted and fixed in formald...
<p>Ba/F3 cells were pre-treated 30 minutes with 0.2 µM TSA or 10 µM α-Br-TMC before being stimulated...
Chromatin-immunoprecipitation (ChIP) employs generally a mild formaldehyde cross-linking step, which...
<div><p>Chromatin-immunoprecipitation (ChIP) employs generally a mild formaldehyde cross-linking ste...
<p>A. HeLa cells were synchronized by nocodazole for 16 h before mitotic cells were separated from a...
<p>Exponentially growing cells were treated with 0.1 mg/ml CHX at 25°C. (A) Cellular amounts of Pol2...
<p>Cells were treated with or without LPS for 1 h. ChIP assays were carried out using an anti-p65 an...