<p>(A) New classic KS case1 and (B) New classic KS case2. Results of ChIP-qPCR at the region of TR, RTA promoter, miR-cluster, vIRF3 and GAPDH gene (control) in classic KS tissue. Samples prepared from new cases of classic KS tissue were used for ChIP-qPCR assay. ChIP–qPCR data were normalized by the percent input method (signals obtained from ChIP were divided by signals obtained from an input sample). Data are presented as mean±SD. <b>N.A.</b> represents no amplification.</p
The advent of high-throughput technologies such as ChIP-seq has made possible the study of histone m...
<p>Primer sets used in RT-qPCR to quantify the KSHV gene expression in iSLK-BAC16 cells.</p
<p>ChIP-seq for SUMO paralogs was performed using chromatin prepared from non-induced (0 hour) and 0...
<p>ChIPs were performed using latently infected SLK cells or SLK cells following <i>de novo</i> infe...
<p>(A) Illustration of epigenetic landscape at the TR region (gi|139472801: 137169–137969). Data wer...
<p>(A) Schematic representation of the human <i>SOX1</i> core promoter analyzed by ChIP. The positio...
<p>(<b>A</b>) Comparative ChIP analysis of H3K4me3, H3K27ac and H3K27me3 at the indicated viral prom...
<p>ChIP assays for the active H3K4me3 and repressive H3K27me3 histone modifications were carried out...
<p>The enlarged map of H3K27me3 histone modification on KSHV genome at higher resolution is illustra...
<p><b>A.</b> Schematic of the KSHV genome with open reading frames indicated. <b>B.</b> Chromatin fr...
<p>(A+B) SLK-shSp100, SLK-shDaxx, SLK-shPML and SLK-shGFP cells were <i>de novo</i> infected with KS...
<p>Chromatin immunoprecipitation (ChIP) was performed with antibodies anti-H3K9ac (A) or anti-H3 (B)...
<p>The three ChIP assays of the MT3 promoter are shown in <a href="http://www.plosone.org/article/in...
<p>(<b>A</b>) SLK cells were transfected with KSHV BAC16 <a href="http://www.plospathogens.org/artic...
<div><p>The advent of high-throughput technologies such as ChIP-seq has made possible the study of h...
The advent of high-throughput technologies such as ChIP-seq has made possible the study of histone m...
<p>Primer sets used in RT-qPCR to quantify the KSHV gene expression in iSLK-BAC16 cells.</p
<p>ChIP-seq for SUMO paralogs was performed using chromatin prepared from non-induced (0 hour) and 0...
<p>ChIPs were performed using latently infected SLK cells or SLK cells following <i>de novo</i> infe...
<p>(A) Illustration of epigenetic landscape at the TR region (gi|139472801: 137169–137969). Data wer...
<p>(A) Schematic representation of the human <i>SOX1</i> core promoter analyzed by ChIP. The positio...
<p>(<b>A</b>) Comparative ChIP analysis of H3K4me3, H3K27ac and H3K27me3 at the indicated viral prom...
<p>ChIP assays for the active H3K4me3 and repressive H3K27me3 histone modifications were carried out...
<p>The enlarged map of H3K27me3 histone modification on KSHV genome at higher resolution is illustra...
<p><b>A.</b> Schematic of the KSHV genome with open reading frames indicated. <b>B.</b> Chromatin fr...
<p>(A+B) SLK-shSp100, SLK-shDaxx, SLK-shPML and SLK-shGFP cells were <i>de novo</i> infected with KS...
<p>Chromatin immunoprecipitation (ChIP) was performed with antibodies anti-H3K9ac (A) or anti-H3 (B)...
<p>The three ChIP assays of the MT3 promoter are shown in <a href="http://www.plosone.org/article/in...
<p>(<b>A</b>) SLK cells were transfected with KSHV BAC16 <a href="http://www.plospathogens.org/artic...
<div><p>The advent of high-throughput technologies such as ChIP-seq has made possible the study of h...
The advent of high-throughput technologies such as ChIP-seq has made possible the study of histone m...
<p>Primer sets used in RT-qPCR to quantify the KSHV gene expression in iSLK-BAC16 cells.</p
<p>ChIP-seq for SUMO paralogs was performed using chromatin prepared from non-induced (0 hour) and 0...