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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP assays were performed using E14Tg2a mouse embryonic stem cells, the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 of the antibody consisting of 1, 2. 5 and 10 μg per ChIP experiment was analysed. IgG (2 μg/IP) was used as negative IP control. Quantitative PCR was performed with primers for known OCT4 targets UTF1, YES1 and ZSCAN10, used as positive control targets, and for the promoter of the GAPDH gene, used as a negative control. 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 OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><small><strong> Figure 3. Determination of the antibody titer</strong><br /> To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against OCT4 (Cat. No. C15410305). The plates were coated with the peptides used for immunization of the rabbit. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:100,000. </small></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 2. ChIP-seq results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><small><strong> Figure 3. Determination of the antibody titer</strong><br /> To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against OCT4 (Cat. No. C15410305). The plates were coated with the peptides used for immunization of the rabbit. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:100,000. </small></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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><strong>ChIP-seq profile</strong> of active (H3K4me3 and H3K36me3) and inactive (H3K27me3) marks using Diagenode antibodies.</p>
<img src="https://www.diagenode.com/img/categories/antibodies/chip-seq-grade-antibodies.png" /></div>
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<p><small> ChIP was performed on sheared chromatin from 100,000 K562 cells using iDeal ChIP-seq kit for Histones (cat. No. C01010051) with 1 µg of the Diagenode antibodies against H3K27me3 (cat. No. C15410195) and H3K4me3 (cat. No. C15410003), and 0.5 µg of the antibody against H3K36me3 (cat. No. C15410192). The IP'd DNA was subsequently analysed on an Illumina Genome Analyzer. Library preparation, cluster generation and sequencing were performed according to the manufacturer's instructions. The 36 bp tags were aligned to the human genome using the ELAND algorithm. The figure shows the signal distribution along the complete sequence of human chromosome 3, a zoomin to a 10 Mb region and a further zoomin to a 1.5 Mb region. </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 OCT4</strong><br /> ChIP assays were performed using E14Tg2a mouse embryonic stem cells, the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 of the antibody consisting of 1, 2. 5 and 10 μg per ChIP experiment was analysed. IgG (2 μg/IP) was used as negative IP control. Quantitative PCR was performed with primers for known OCT4 targets UTF1, YES1 and ZSCAN10, used as positive control targets, and for the promoter of the GAPDH gene, used as a negative control. 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 OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><small><strong> Figure 3. Determination of the antibody titer</strong><br /> To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against OCT4 (Cat. No. C15410305). The plates were coated with the peptides used for immunization of the rabbit. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:100,000. </small></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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/C15410305-chip.png" alt="OCT4 Antibody ChIP Grade" caption="false" width="288" height="209" /></p>
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP assays were performed using E14Tg2a mouse embryonic stem cells, the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 of the antibody consisting of 1, 2. 5 and 10 μg per ChIP experiment was analysed. IgG (2 μg/IP) was used as negative IP control. Quantitative PCR was performed with primers for known OCT4 targets UTF1, YES1 and ZSCAN10, used as positive control targets, and for the promoter of the GAPDH gene, used as a negative control. 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/C15410305-chipseq-fig1.png" alt="OCT4 Antibody ChIP-seq Grade" caption="false" width="288" height="34" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-chipseq-fig2.png" alt="OCT4 Antibody for ChIP-seq" caption="false" width="288" height="52" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-chipseq-fig3.png" alt="OCT4 Antibody for ChIP-seq assay" caption="false" width="288" height="38" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-chipseq-fig4.png" alt="OCT4 Antibody validated in ChIP-seq" caption="false" width="288" height="57" /></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-ELISA.png" alt="OCT4 Antibody for ELISA validation" caption="false" width="288" height="219" /></p>
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<div class="small-8 columns">
<p><small><strong> Figure 3. Determination of the antibody titer</strong><br /> To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against OCT4 (Cat. No. C15410305). The plates were coated with the peptides used for immunization of the rabbit. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:100,000. </small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-WB.png" alt="OCT4 Antibody validated in Western Blot" caption="false" width="123" height="167" /></p>
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<div class="small-8 columns">
<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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>Learn more about: <a href="https://www.diagenode.com/applications/western-blot">Loading control, MW marker visualization</a><em>. <br /></em></p>
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<p><strong>ChIP-seq profile</strong> of active (H3K4me3 and H3K36me3) and inactive (H3K27me3) marks using Diagenode antibodies.</p>
<img src="https://www.diagenode.com/img/categories/antibodies/chip-seq-grade-antibodies.png" /></div>
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<p><small> ChIP was performed on sheared chromatin from 100,000 K562 cells using iDeal ChIP-seq kit for Histones (cat. No. C01010051) with 1 µg of the Diagenode antibodies against H3K27me3 (cat. No. C15410195) and H3K4me3 (cat. No. C15410003), and 0.5 µg of the antibody against H3K36me3 (cat. No. C15410192). The IP'd DNA was subsequently analysed on an Illumina Genome Analyzer. Library preparation, cluster generation and sequencing were performed according to the manufacturer's instructions. The 36 bp tags were aligned to the human genome using the ELAND algorithm. The figure shows the signal distribution along the complete sequence of human chromosome 3, a zoomin to a 10 Mb region and a further zoomin to a 1.5 Mb region. </small></p>
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<p>Diagenode’s highly validated antibodies:</p>
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<p><br />Chromatin immunoprecipitation (<b>ChIP</b>) is a technique to study the associations of proteins with the specific genomic regions in intact cells. One of the most important steps of this protocol is the immunoprecipitation of targeted protein using the antibody specifically recognizing it. The quality of antibodies used in ChIP is essential for the success of the experiment. Diagenode offers extensively validated ChIP-grade antibodies, confirmed for their specificity, and high level of performance in ChIP. Each batch is validated, and batch-specific data are available on the website.</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>Diagenode has partnered with leading epigenetics experts and numerous epigenetics consortiums to bring to you a validated and comprehensive collection of epigenetic antibodies. As an expert in epigenetics, we are committed to offering highly-specific antibodies validated for ChIP/ChIP-seq and many other applications. All batch-specific validation data is available on our website.<br /><a href="../categories/antibodies">Read about our expertise in antibody production</a>.</p>
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View::render() - CORE/Cake/View/View.php, line 473
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<p><small><strong> Figure 1. ChIP results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP assays were performed using E14Tg2a mouse embryonic stem cells, the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 of the antibody consisting of 1, 2. 5 and 10 μg per ChIP experiment was analysed. IgG (2 μg/IP) was used as negative IP control. Quantitative PCR was performed with primers for known OCT4 targets UTF1, YES1 and ZSCAN10, used as positive control targets, and for the promoter of the GAPDH gene, used as a negative control. 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 3. Determination of the antibody titer</strong><br /> To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against OCT4 (Cat. No. C15410305). The plates were coated with the peptides used for immunization of the rabbit. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:100,000. </small></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 2. ChIP-seq results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 2. ChIP-seq results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-WB.png" alt="OCT4 Antibody validated in Western Blot" caption="false" width="123" height="167" /></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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>Learn more about: <a href="https://www.diagenode.com/applications/western-blot">Loading control, MW marker visualization</a><em>. <br /></em></p>
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<p><strong>ChIP-seq profile</strong> of active (H3K4me3 and H3K36me3) and inactive (H3K27me3) marks using Diagenode antibodies.</p>
<img src="https://www.diagenode.com/img/categories/antibodies/chip-seq-grade-antibodies.png" /></div>
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<p><small> ChIP was performed on sheared chromatin from 100,000 K562 cells using iDeal ChIP-seq kit for Histones (cat. No. C01010051) with 1 µg of the Diagenode antibodies against H3K27me3 (cat. No. C15410195) and H3K4me3 (cat. No. C15410003), and 0.5 µg of the antibody against H3K36me3 (cat. No. C15410192). The IP'd DNA was subsequently analysed on an Illumina Genome Analyzer. Library preparation, cluster generation and sequencing were performed according to the manufacturer's instructions. The 36 bp tags were aligned to the human genome using the ELAND algorithm. The figure shows the signal distribution along the complete sequence of human chromosome 3, a zoomin to a 10 Mb region and a further zoomin to a 1.5 Mb region. </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 OCT4</strong><br /> ChIP assays were performed using E14Tg2a mouse embryonic stem cells, the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 of the antibody consisting of 1, 2. 5 and 10 μg per ChIP experiment was analysed. IgG (2 μg/IP) was used as negative IP control. Quantitative PCR was performed with primers for known OCT4 targets UTF1, YES1 and ZSCAN10, used as positive control targets, and for the promoter of the GAPDH gene, used as a negative control. 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/C15410305-chipseq-fig2.png" alt="OCT4 Antibody for ChIP-seq" caption="false" width="288" height="52" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-chipseq-fig3.png" alt="OCT4 Antibody for ChIP-seq assay" caption="false" width="288" height="38" /></p>
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<p><small><strong> Figure 2. ChIP-seq results obtained with the Diagenode antibody directed against OCT4</strong><br /> ChIP was performed on sheared chromatin from 4 million E14Tg2a mouse embryonic stem cells using 5 μg of the Diagenode antibody against OCT4 (Cat. No. C15410305) 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 51 bp tags were aligned to the mouse genome using the BWA algorithm. Figure 2 shows the peak distribution along the complete sequence of mouse chromosome 7 (figure 2A) and a 1Mb region containing the UTF1 positive control (figure 2B), and in a two genomic regions surrounding the YES1 and ZSCAN10 positive control genes (figure 2C and D). </small></p>
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<p><small><strong> Figure 3. Determination of the antibody titer</strong><br /> To determine the titer of the antibody, an ELISA was performed using a serial dilution of the Diagenode antibody directed against OCT4 (Cat. No. C15410305). The plates were coated with the peptides used for immunization of the rabbit. By plotting the absorbance against the antibody dilution (Figure 2), the titer of the antibody was estimated to be 1:100,000. </small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410305-WB.png" alt="OCT4 Antibody validated in Western Blot" caption="false" width="123" height="167" /></p>
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<p><small><strong> Figure 4. Western blot analysis using the Diagenode antibody directed against OCT4</strong><br /> Nuclear extracts (15 μg) from human embryonic stem cells were analysed by Western blot using the Diagenode antibody against OCT4 (Cat. No. C15410305) 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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include - APP/View/Products/view.ctp, line 755
View::_evaluate() - CORE/Cake/View/View.php, line 971
View::_render() - CORE/Cake/View/View.php, line 933
View::render() - CORE/Cake/View/View.php, line 473
Controller::render() - CORE/Cake/Controller/Controller.php, line 963
ProductsController::slug() - APP/Controller/ProductsController.php, line 1052
ReflectionMethod::invokeArgs() - [internal], line ??
Controller::invokeAction() - CORE/Cake/Controller/Controller.php, line 491
Dispatcher::_invoke() - CORE/Cake/Routing/Dispatcher.php, line 193
Dispatcher::dispatch() - CORE/Cake/Routing/Dispatcher.php, line 167
[main] - APP/webroot/index.php, line 118
×