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'description' => '<p>Polyclonal antibody raised in rabbit against human JARID1C (Jumonji, AT Rich Interactive Domain 1C), using a synthetic peptide containing a sequence from the central part of the protein<sup>1</sup>.</p><p><small><sup>1</sup>Manufactured by Bethyl Laboratories, Inc., Texas, USA</small></p>',
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chip.jpg" alt="JARID1C Antibody ChIP Grade" caption="false" width="447" height="339" /></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-c.jpg" alt="JARID1C Antibody for ChIP-seq assay" caption="false" width="700" height="178" /></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-wb.jpg" alt="JARID1C Antibody validated in Western blot" width="223" height="294" caption="false" /></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-ip.jpg" alt="JARID1C Antibody validated in Immunoprecipitation " width="145" height="255" caption="false" /></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<td>ChIP/ChIP-seq <sup>*</sup></td>
<td>5 μg/ChIP</td>
<td>Fig 1, 2</td>
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<td>Fig 4</td>
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<p><small><sup>*</sup> Please note that the optimal antibody amount per IP should be determined by the end-user. We recommend testing 0.5-5 μg per IP.</small></p>
<p><small><sup>1</sup>Manufactured by Bethyl Laboratories, Inc., Texas, USA</small></p>',
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'description' => '<p>Polyclonal antibody raised in rabbit against human JARID1C (Jumonji, AT Rich Interactive Domain 1C), using a synthetic peptide containing a sequence from the central part of the protein<sup>1</sup>.</p><p><small><sup>1</sup>Manufactured by Bethyl Laboratories, Inc., Texas, USA</small></p>',
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chip.jpg" alt="JARID1C Antibody ChIP Grade" caption="false" width="447" height="339" /></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-a.jpg" alt="JARID1C Antibody ChIP-seq Grade" caption="false" width="700" height="83" /></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-c.jpg" alt="JARID1C Antibody for ChIP-seq assay" caption="false" width="700" height="178" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-d.jpg" alt="JARID1C Antibody validated in ChIP-seq" caption="false" width="700" height="130" /></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-wb.jpg" alt="JARID1C Antibody validated in Western blot" width="223" height="294" caption="false" /></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<th>Suggested dilution</th>
<th>References</th>
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<td>ChIP/ChIP-seq <sup>*</sup></td>
<td>5 μg/ChIP</td>
<td>Fig 1, 2</td>
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<tr>
<td>Western Blotting</td>
<td>1:100</td>
<td>Fig 3</td>
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<td>IP</td>
<td>6 μg per IP</td>
<td>Fig 4</td>
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<p><small><sup>*</sup> Please note that the optimal antibody amount per IP should be determined by the end-user. We recommend testing 0.5-5 μg per IP.</small></p>
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<div class="small-6 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chip.jpg" alt="JARID1C Antibody ChIP Grade" caption="false" width="447" height="339" /></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<div class="small-12 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-a.jpg" alt="JARID1C Antibody ChIP-seq Grade" caption="false" width="700" height="83" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-b.jpg" alt="JARID1C Antibody for ChIP-seq" caption="false" width="700" height="164" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-c.jpg" alt="JARID1C Antibody for ChIP-seq assay" caption="false" width="700" height="178" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-d.jpg" alt="JARID1C Antibody validated in ChIP-seq" caption="false" width="700" height="130" /></p>
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<div class="row">
<div class="small-12 columns">
<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
</div>
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<div class="row">
<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-wb.jpg" alt="JARID1C Antibody validated in Western blot" width="223" height="294" caption="false" /></p>
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<div class="small-8 columns">
<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<div class="row">
<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-ip.jpg" alt="JARID1C Antibody validated in Immunoprecipitation " width="145" height="255" caption="false" /></p>
</div>
<div class="small-8 columns">
<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><strong>ChIP results</strong> obtained with the antibody directed against H3K4me3 (Cat. No. <a href="../p/h3k4me3-polyclonal-antibody-premium-50-ug-50-ul">C15410003</a>). </p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chip.jpg" alt="JARID1C Antibody ChIP Grade" caption="false" width="447" height="339" /></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-ip.jpg" alt="JARID1C Antibody validated in Immunoprecipitation " width="145" height="255" caption="false" /></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<td>ChIP/ChIP-seq <sup>*</sup></td>
<td>5 μg/ChIP</td>
<td>Fig 1, 2</td>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<div class="small-12 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-a.jpg" alt="JARID1C Antibody ChIP-seq Grade" caption="false" width="700" height="83" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-b.jpg" alt="JARID1C Antibody for ChIP-seq" caption="false" width="700" height="164" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-c.jpg" alt="JARID1C Antibody for ChIP-seq assay" caption="false" width="700" height="178" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-d.jpg" alt="JARID1C Antibody validated in ChIP-seq" caption="false" width="700" height="130" /></p>
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<div class="small-12 columns">
<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-wb.jpg" alt="JARID1C Antibody validated in Western blot" width="223" height="294" caption="false" /></p>
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<div class="small-8 columns">
<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-ip.jpg" alt="JARID1C Antibody validated in Immunoprecipitation " width="145" height="255" caption="false" /></p>
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<div class="small-8 columns">
<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><strong>ChIP results</strong> obtained with the antibody directed against H3K4me3 (Cat. No. <a href="../p/h3k4me3-polyclonal-antibody-premium-50-ug-50-ul">C15410003</a>). </p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-c.jpg" alt="JARID1C Antibody for ChIP-seq assay" caption="false" width="700" height="178" /></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-ip.jpg" alt="JARID1C Antibody validated in Immunoprecipitation " width="145" height="255" caption="false" /></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<div class="small-12 columns">
<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-a.jpg" alt="JARID1C Antibody ChIP-seq Grade" caption="false" width="700" height="83" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-b.jpg" alt="JARID1C Antibody for ChIP-seq" caption="false" width="700" height="164" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-c.jpg" alt="JARID1C Antibody for ChIP-seq assay" caption="false" width="700" height="178" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-d.jpg" alt="JARID1C Antibody validated in ChIP-seq" caption="false" width="700" height="130" /></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-wb.jpg" alt="JARID1C Antibody validated in Western blot" width="223" height="294" caption="false" /></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-ip.jpg" alt="JARID1C Antibody validated in Immunoprecipitation " width="145" height="255" caption="false" /></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP assays were performed using K562 cells, the Diagenode antibody against JARID1C (Cat. No. C15410338) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (Cat. No. C01010055), using sheared chromatin from 4 million cells. A titration consisting of 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (2 μg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoter of the active EIF4A2 gene, used as positive control, and for the MYOD1 gene and Sat2 satellite repeat, used as negative controls. Figure 1 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410338-chipseq-a.jpg" alt="JARID1C Antibody ChIP-seq Grade" caption="false" width="700" height="83" /></p>
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<div class="small-12 columns">
<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against JARID1C</strong><br />ChIP was performed on sheared chromatin from 4 million K562 cells using 5 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338) as described above. The IP’d DNA was subsequently analysed on an Illumina HiSeq. Library preparation, cluster generation and sequencing were performed according to the manufacturer’s instructions. The 50 bp tags were aligned to the human genome using the BWA algorithm. Figure 2 shows the enrichment along the complete sequence and a 600 Kb region of the human chromosome 1 (fig 2A and B), and in two genomic regions surrounding the ALDOA gene and the EIF4A2 positive control gene (fig 2C and D).</small></p>
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<p><small><strong> Figure 3. Western blot analysis using the Diagenode antibody directed against JARID1C</strong><br />Whole cell extracts from HeLa cells were analysed by Western blot using the Diagenode antibody against JARID1C (Cat. No. C15410338) diluted 1:1,000 in TBS-Tween containing 5% skimmed milk. The position of the protein of interest is indicated on the right; the marker (in kDa) is shown on the left.</small></p>
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<p><small><strong> Figure 4. Immunoprecipitation using the Diagenode antibody directed against JARID1C</strong><br />Immunoprecipitation was performed on whole cell extracts from HeLa cells using 6 μg of the Diagenode antibody against JARID1C (Cat. No. C15410338, lane 1). An equal amount of rabbit IgG was used as a negative control (lane 2). The immunoprecipitated JARID1C protein was detected by western blot with the JARID1C antibody diluted 1:200.</small></p>
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