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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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 monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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/c15210003-if.png" alt="macroH2A.1/H2A.2 Antibody validated in Immunofluorescence" caption="false" width="288" height="288" /></p>
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<p><small> <strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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<td>1:2,000</td>
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'name' => 'macroH2A.1/H2A.2 Antibody - ChIP-seq Grade',
'description' => '<p>Monoclonal antibody raised in rabbit against histone macroH2A.1, using a KLH-conjugated synthetic peptide from the C-terminus of the protein. The antibody also recognizes macroH2A.2</p>',
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<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chip.jpg" alt="macroH2A.1/H2A.2 Antibody ChIP Grade" caption="false" width="288" height="219" /></p>
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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 monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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Two core histones of each class H2A, H2B, H3 and H4 assemble and are wrapped by 146 base pairs of DNA to form one
octameric nucleosome. Histone tails undergo numerous post-translational modifications, which either directly or indirectly
alter chromatin structure to facilitate transcriptional activation or repression or other nuclear processes. In addition to the
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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/c15210003-chipseq-a.jpg" alt="macroH2A.1/H2A.2 Antibody ChIP-seq Grade" caption="false" width="288" height="82" /></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chipseq-c.jpg" alt="macroH2A.1/H2A.2 Antibody for ChIP-seq assay" caption="false" width="288" height="72" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chipseq-d.jpg" alt="macroH2A.1/H2A.2 Antibody validated in ChIP-seq" caption="false" width="288" height="73" /></p>
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<p><small> <strong>Figure 2. ChIP-seq results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-wb.png" alt="macroH2A.1/H2A.2 Antibody validated in Western Blot" caption="false" width="288" height="263" /></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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/c15210003-if.png" alt="macroH2A.1/H2A.2 Antibody validated in Immunofluorescence" caption="false" width="288" height="288" /></p>
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<p><small> <strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</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><img src="https://www.diagenode.com/img/product/antibodies/C15200229-IF.jpg" alt="" height="245" width="256" /></p>
<p><sup><strong>Immunofluorescence using the Diagenode monoclonal antibody directed against CRISPR/Cas9</strong></sup></p>
<p><sup>HeLa cells transfected with a Cas9 expression vector (left) or untransfected cells (right) were fixed in methanol at -20°C, permeabilized with acetone at -20°C and blocked with PBS containing 2% BSA. The cells were stained with the Cas9 C-terminal antibody (Cat. No. C15200229) diluted 1:400, followed by incubation with an anti-mouse secondary antibody coupled to AF488. The bottom images show counter-staining of the nuclei with Hoechst 33342.</sup></p>
<h5><sup>Check our selection of antibodies validated in IF.</sup></h5>',
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<p><span style="font-weight: 400;">Diagenode’s highly validated antibodies:</span></p>
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<li>Highly sensitive and specific</li>
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<p>The core histones have a globular structure with large unstructured N-terminal tails protruding from the nucleosome. They can undergo to multiple post-translational modifications (PTM), mainly at the N-terminal tails. These <strong>post-translational modifications </strong>include methylation, acetylation, phosphorylation, ubiquitinylation, citrullination, sumoylation, deamination and crotonylation. The most well characterized PTMs are <strong>methylation,</strong> <strong>acetylation and phosphorylation</strong>. Histone methylation occurs mainly on lysine (K) residues, which can be mono-, di- or tri-methylated, and on arginines (R), which can be mono-methylated and symmetrically or asymmetrically di-methylated. Histone acetylation occurs on lysines and histone phosphorylation mainly on serines (S), threonines (T) and tyrosines (Y).</p>
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<p><img src="https://www.diagenode.com/img/categories/antibodies/histone-marks-illustration.png" /></p>
<p>Diagenode is proud to offer a large range of antibodies against histones and histone modifications. Our antibodies are highly specific and have been validated in many applications, including <strong>ChIP</strong> and <strong>ChIP-seq</strong>.</p>
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<li><strong>Histone H2B and H2B</strong> <strong>modifications </strong>(serine phosphorylation, lysine acetylation)</li>
<li><strong>Histone H3 and H3 modifications </strong>(lysine methylation (mono-, di- and tri-methylated), lysine acetylation, serine phosphorylation, threonine phosphorylation, arginine methylation (mono-methylated, symmetrically and asymmetrically di-methylated))</li>
<li><strong>Histone H4 and H4 modifications (</strong>lysine methylation (mono-, di- and tri-methylated), lysine acetylation, arginine methylation (mono-methylated and symmetrically di-methylated), serine phosphorylation )</li>
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<p><span style="font-weight: 400;"><strong>HDAC's HAT's, HMT's and other</strong> <strong>enzymes</strong> which modify histones can be found in the category <a href="../categories/chromatin-modifying-proteins-histone-transferase">Histone modifying enzymes</a><br /></span></p>
<p><span style="font-weight: 400;"> Diagenode’s highly validated antibodies:</span></p>
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<li><span style="font-weight: 400;"> Expert technical support</span></li>
<li><span style="font-weight: 400;"> Sample sizes available</span></li>
<li><span style="font-weight: 400;"> 100% satisfaction guarantee</span></li>
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<p><strong>ChIP-seq profile</strong> of active (H3K4me3 and H3K36me3) and inactive (H3K27me3) marks using Diagenode antibodies.</p>
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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><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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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'info2' => '<p>Histones are the main constituents of the protein part of chromosomes of eukaryotic cells. They are rich in the amino acids arginine and lysine and have been greatly conserved during evolution. Histones pack the DNA into tight masses of chromatin. Two core histones of each class H2A, H2B, H3 and H4 assemble and are wrapped by 146 base pairs of DNA to form one octameric nucleosome. Histone tails undergo numerous post-translational modifications, which either directly or indirectly alter chromatin structure to facilitate transcriptional activation or repression or other nuclear processes. In addition to the genetic code, combinations of the different histone modifications reveal the so-called "histone code". Histone methylation and demethylation is dynamically regulated by respectively histone methyl transferases and histone demethylases. macroH2A.1 is an histone variant which replaces H2A in some nucleosomes and represses transcription.</p>',
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'meta_title' => 'Histone macroH2A1 Antibody - ChIP-seq Grade (C15210003) | Diagenode',
'meta_keywords' => ' Histone macroH2A1 Monoclonal Antibody,Immunofluorescence,Western blot',
'meta_description' => 'Histone macroH2A1 Monoclonal Antibody validated in ChIP-seq, ChIP-qPCR WB and IF. Batch-specific data available on the website. ',
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'name' => 'macroH2A.1 monoclonal antibody',
'description' => 'Histones are the main constituents of the protein part of chromosomes of eukaryotic cells. They are rich in the amino acids
arginine and lysine and have been greatly conserved during evolution. Histones pack the DNA into tight masses of chromatin.
Two core histones of each class H2A, H2B, H3 and H4 assemble and are wrapped by 146 base pairs of DNA to form one
octameric nucleosome. Histone tails undergo numerous post-translational modifications, which either directly or indirectly
alter chromatin structure to facilitate transcriptional activation or repression or other nuclear processes. In addition to the
genetic code, combinations of the different histone modifications reveal the so-called “histone code”. Histone methylation and
demethylation is dynamically regulated by respectively histone methyl transferases and histone demethylases. macroH2A.1 is
an histone variant which replaces H2A in some nucleosomes and represses transcription.',
'clonality' => '',
'isotype' => '',
'lot' => '002',
'concentration' => '1 μg/μl',
'reactivity' => 'Human',
'type' => 'Monoclonal',
'purity' => 'Protein A purified',
'classification' => 'Classic',
'application_table' => '<table>
<thead>
<tr>
<th>Applications</th>
<th>Suggested dilution</th>
<th>References</th>
</tr>
</thead>
<tbody>
<tr>
<td>ChIP /ChIP-seq *</td>
<td>0.5 - 1 μg/ChIP</td>
<td>Fig 1, 2</td>
</tr>
<tr>
<td>Western Blotting</td>
<td>1:2,000</td>
<td>Fig 3</td>
</tr>
<tr>
<td>Immunofluorescence</td>
<td>1:500</td>
<td>Fig 4</td>
</tr>
</tbody>
</table>
<p><small>* Please note that the optimal antibody amount per ChIP should be determined by the end-user. We recommend testing 0.5-5 μg per ChIP.</small></p>',
'storage_conditions' => 'Store at -20°C; for long storage, store at -80°C. Avoid multiple freeze-thaw cycles.',
'storage_buffer' => '',
'precautions' => 'This product is for research use only. Not for use in diagnostic or therapeutic procedures.',
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'slug' => 'macroh2a1-monoclonal-antibody',
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'modified' => '2021-12-15 13:24:15',
'created' => '2016-10-19 10:38:21',
'select_label' => '489 - macroH2A.1 monoclonal antibody (002 - 1 μg/μl - Human - Protein A purified - Rabbit)'
),
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'name' => 'macroH2A.1/H2A.2 Antibody',
'description' => '<p>Monoclonal antibody raised in rabbit against <strong>histone</strong> <strong>macroH2A.1</strong>, using a KLH-conjugated synthetic peptide from the C-terminus of the protein. The antibody also recognizes macroH2A.2</p>',
'label1' => 'Validation Data',
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<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chip.jpg" alt="macroH2A.1/H2A.2 Antibody ChIP Grade" caption="false" width="288" height="219" /></p>
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<div class="small-8 columns">
<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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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</div>
<div class="row">
<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chipseq-a.jpg" alt="macroH2A.1/H2A.2 Antibody ChIP-seq Grade" caption="false" width="288" height="82" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chipseq-b.jpg" alt="macroH2A.1/H2A.2 Antibody for ChIP-seq" caption="false" width="288" height="91" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chipseq-c.jpg" alt="macroH2A.1/H2A.2 Antibody for ChIP-seq assay" caption="false" width="288" height="72" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-chipseq-d.jpg" alt="macroH2A.1/H2A.2 Antibody validated in ChIP-seq" caption="false" width="288" height="73" /></p>
</div>
<div class="small-8 columns">
<p><small> <strong>Figure 2. ChIP-seq results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
</div>
</div>
<div class="row">
<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-wb.png" alt="macroH2A.1/H2A.2 Antibody validated in Western Blot" caption="false" width="288" height="263" /></p>
</div>
<div class="small-8 columns">
<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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>
</div>
</div>
<div class="row">
<div class="small-4 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/c15210003-if.png" alt="macroH2A.1/H2A.2 Antibody validated in Immunofluorescence" caption="false" width="288" height="288" /></p>
</div>
<div class="small-8 columns">
<p><small> <strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
</div>
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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>
<p><em></em>Check our selection of antibodies validated in Western blot.</p>',
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<p>Diagenode offers huge selection of highly sensitive antibodies validated in IF.</p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15200229-IF.jpg" alt="" height="245" width="256" /></p>
<p><sup><strong>Immunofluorescence using the Diagenode monoclonal antibody directed against CRISPR/Cas9</strong></sup></p>
<p><sup>HeLa cells transfected with a Cas9 expression vector (left) or untransfected cells (right) were fixed in methanol at -20°C, permeabilized with acetone at -20°C and blocked with PBS containing 2% BSA. The cells were stained with the Cas9 C-terminal antibody (Cat. No. C15200229) diluted 1:400, followed by incubation with an anti-mouse secondary antibody coupled to AF488. The bottom images show counter-staining of the nuclei with Hoechst 33342.</sup></p>
<h5><sup>Check our selection of antibodies validated in IF.</sup></h5>',
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'description' => '<p><span style="font-weight: 400;">All Diagenode’s antibodies are listed below. Please, use our Quick search field to find the antibody of interest by target name, application, purity.</span></p>
<p><span style="font-weight: 400;">Diagenode’s highly validated antibodies:</span></p>
<ul>
<li>Highly sensitive and specific</li>
<li>Cost-effective (requires less antibody per reaction)</li>
<li>Batch-specific data is available on the website</li>
<li>Expert technical support</li>
<li>Sample sizes available</li>
<li>100% satisfaction guarantee</li>
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'description' => '<p>Histones are the main protein components of chromatin involved in the compaction of DNA into nucleosomes, the basic units of chromatin. A <strong>nucleosome</strong> consists of one pair of each of the core histones (<strong>H2A</strong>, <strong>H2B</strong>, <strong>H3</strong> and <strong>H4</strong>) forming an octameric structure wrapped by 146 base pairs of DNA. The different nucleosomes are linked by the linker histone<strong> H1, </strong>allowing for further condensation of chromatin.</p>
<p>The core histones have a globular structure with large unstructured N-terminal tails protruding from the nucleosome. They can undergo to multiple post-translational modifications (PTM), mainly at the N-terminal tails. These <strong>post-translational modifications </strong>include methylation, acetylation, phosphorylation, ubiquitinylation, citrullination, sumoylation, deamination and crotonylation. The most well characterized PTMs are <strong>methylation,</strong> <strong>acetylation and phosphorylation</strong>. Histone methylation occurs mainly on lysine (K) residues, which can be mono-, di- or tri-methylated, and on arginines (R), which can be mono-methylated and symmetrically or asymmetrically di-methylated. Histone acetylation occurs on lysines and histone phosphorylation mainly on serines (S), threonines (T) and tyrosines (Y).</p>
<p>The PTMs of the different residues are involved in numerous processes such as DNA repair, DNA replication and chromosome condensation. They influence the chromatin organization and can be positively or negatively associated with gene expression. Trimethylation of H3K4, H3K36 and H3K79, and lysine acetylation generally result in an open chromatin configuration (figure below) and are therefore associated with <strong>euchromatin</strong> and gene activation. Trimethylation of H3K9, K3K27 and H4K20, on the other hand, is enriched in <strong>heterochromatin </strong>and associated with gene silencing. The combination of different histone modifications is called the "<strong>histone code</strong>”, analogous to the genetic code.</p>
<p><img src="https://www.diagenode.com/img/categories/antibodies/histone-marks-illustration.png" /></p>
<p>Diagenode is proud to offer a large range of antibodies against histones and histone modifications. Our antibodies are highly specific and have been validated in many applications, including <strong>ChIP</strong> and <strong>ChIP-seq</strong>.</p>
<p>Diagenode’s collection includes antibodies recognizing:</p>
<ul>
<li><strong>Histone H1 variants</strong></li>
<li><strong>Histone H2A, H2A variants and histone H2A</strong> <strong>modifications</strong> (serine phosphorylation, lysine acetylation, lysine ubiquitinylation)</li>
<li><strong>Histone H2B and H2B</strong> <strong>modifications </strong>(serine phosphorylation, lysine acetylation)</li>
<li><strong>Histone H3 and H3 modifications </strong>(lysine methylation (mono-, di- and tri-methylated), lysine acetylation, serine phosphorylation, threonine phosphorylation, arginine methylation (mono-methylated, symmetrically and asymmetrically di-methylated))</li>
<li><strong>Histone H4 and H4 modifications (</strong>lysine methylation (mono-, di- and tri-methylated), lysine acetylation, arginine methylation (mono-methylated and symmetrically di-methylated), serine phosphorylation )</li>
</ul>
<p><span style="font-weight: 400;"><strong>HDAC's HAT's, HMT's and other</strong> <strong>enzymes</strong> which modify histones can be found in the category <a href="../categories/chromatin-modifying-proteins-histone-transferase">Histone modifying enzymes</a><br /></span></p>
<p><span style="font-weight: 400;"> Diagenode’s highly validated antibodies:</span></p>
<ul>
<li><span style="font-weight: 400;"> Highly sensitive and specific</span></li>
<li><span style="font-weight: 400;"> Cost-effective (requires less antibody per reaction)</span></li>
<li><span style="font-weight: 400;"> Batch-specific data is available on the website</span></li>
<li><span style="font-weight: 400;"> Expert technical support</span></li>
<li><span style="font-weight: 400;"> Sample sizes available</span></li>
<li><span style="font-weight: 400;"> 100% satisfaction guarantee</span></li>
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<p><span style="font-weight: 400;">Diagenode provides leading solutions for epigenetic research. Because ChIP-seq is a widely-used technique, we validate our antibodies in ChIP and ChIP-seq experiments (in addition to conventional methods like Western blot, Dot blot, ELISA, and immunofluorescence) to provide the highest quality antibody. We standardize our validation and production to guarantee high product quality without technical bias. Diagenode guarantees ChIP-seq grade antibody performance under our suggested conditions.</span></p>
<div class="row">
<div class="small-12 medium-9 large-9 columns">
<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>
<div class="small-12 medium-3 large-3 columns">
<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>
<ul>
<li>Highly sensitive and specific</li>
<li>Cost-effective (requires less antibody per reaction)</li>
<li>Batch-specific data is available on the website</li>
<li>Expert technical support</li>
<li>Sample sizes available</li>
<li>100% satisfaction guarantee</li>
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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 monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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 monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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<p><small> <strong>Figure 2. ChIP-seq results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</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><sup><strong>Immunofluorescence using the Diagenode monoclonal antibody directed against CRISPR/Cas9</strong></sup></p>
<p><sup>HeLa cells transfected with a Cas9 expression vector (left) or untransfected cells (right) were fixed in methanol at -20°C, permeabilized with acetone at -20°C and blocked with PBS containing 2% BSA. The cells were stained with the Cas9 C-terminal antibody (Cat. No. C15200229) diluted 1:400, followed by incubation with an anti-mouse secondary antibody coupled to AF488. The bottom images show counter-staining of the nuclei with Hoechst 33342.</sup></p>
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<p><img src="https://www.diagenode.com/img/categories/antibodies/histone-marks-illustration.png" /></p>
<p>Diagenode is proud to offer a large range of antibodies against histones and histone modifications. Our antibodies are highly specific and have been validated in many applications, including <strong>ChIP</strong> and <strong>ChIP-seq</strong>.</p>
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<li><strong>Histone H2B and H2B</strong> <strong>modifications </strong>(serine phosphorylation, lysine acetylation)</li>
<li><strong>Histone H3 and H3 modifications </strong>(lysine methylation (mono-, di- and tri-methylated), lysine acetylation, serine phosphorylation, threonine phosphorylation, arginine methylation (mono-methylated, symmetrically and asymmetrically di-methylated))</li>
<li><strong>Histone H4 and H4 modifications (</strong>lysine methylation (mono-, di- and tri-methylated), lysine acetylation, arginine methylation (mono-methylated and symmetrically di-methylated), serine phosphorylation )</li>
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<p><span style="font-weight: 400;"><strong>HDAC's HAT's, HMT's and other</strong> <strong>enzymes</strong> which modify histones can be found in the category <a href="../categories/chromatin-modifying-proteins-histone-transferase">Histone modifying enzymes</a><br /></span></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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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
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</small></p>
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alter chromatin structure to facilitate transcriptional activation or repression or other nuclear processes. In addition to the
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<p><small> <strong>Figure 1. ChIP results obtained with the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP assays were performed using HeLa cells, the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) and optimized PCR primer sets for qPCR. ChIP was performed with the “iDeal ChIP-seq” kit (cat. No. C01010051), using sheared chromatin from 1 million cells. A titration consisting of 0.5, 1, 2 and 5 μg of antibody per ChIP experiment was analyzed. IgG (1 μg/IP) was used as a negative IP control. Quantitative PCR was performed with optimized primers for the MYT1 and HBB genes and for the Sat2 satellite repeat, used as positive controls, and for the GAPDH promoter, used as 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 monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />ChIP was performed on sheared chromatin from 1 million HeLa cells using 0.5 μg of the Diagenode antibody against macroH2A.1/H2A.2 (cat. No. C15210003) 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 in 4 genomic regions of chromosome 20 (including the MYT1 positive control gene), 6, 11 and 3, respectively.</small></p>
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<p><small> <strong>Figure 3. Western blot analysis using the Diagenode monoclonal antibody directed against macroH2A.1</strong><br />Histone extracts from HeLa cells were analysed by Western blot using the Diagenode monoclonal antibody against macroH2A.1/H2A.2 (Cat. No. C15210003) diluted 1:2,000 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/c15210003-if.png" alt="macroH2A.1/H2A.2 Antibody validated in Immunofluorescence" caption="false" width="288" height="288" /></p>
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<p><small> <strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against macroH2A.1/H2A.2</strong><br />HeLa cells were stained with the Diagenode antibody against macroH2A.1/H2A.2 (Cat. No. C15210003, red) diluted 1:500. Actin filaments were stained with fluorescein phalladoin (green).</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><sup><strong>Immunofluorescence using the Diagenode monoclonal antibody directed against CRISPR/Cas9</strong></sup></p>
<p><sup>HeLa cells transfected with a Cas9 expression vector (left) or untransfected cells (right) were fixed in methanol at -20°C, permeabilized with acetone at -20°C and blocked with PBS containing 2% BSA. The cells were stained with the Cas9 C-terminal antibody (Cat. No. C15200229) diluted 1:400, followed by incubation with an anti-mouse secondary antibody coupled to AF488. The bottom images show counter-staining of the nuclei with Hoechst 33342.</sup></p>
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<p><span style="font-weight: 400;">Diagenode’s highly validated antibodies:</span></p>
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<li>Highly sensitive and specific</li>
<li>Cost-effective (requires less antibody per reaction)</li>
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<p>The core histones have a globular structure with large unstructured N-terminal tails protruding from the nucleosome. They can undergo to multiple post-translational modifications (PTM), mainly at the N-terminal tails. These <strong>post-translational modifications </strong>include methylation, acetylation, phosphorylation, ubiquitinylation, citrullination, sumoylation, deamination and crotonylation. The most well characterized PTMs are <strong>methylation,</strong> <strong>acetylation and phosphorylation</strong>. Histone methylation occurs mainly on lysine (K) residues, which can be mono-, di- or tri-methylated, and on arginines (R), which can be mono-methylated and symmetrically or asymmetrically di-methylated. Histone acetylation occurs on lysines and histone phosphorylation mainly on serines (S), threonines (T) and tyrosines (Y).</p>
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<p><img src="https://www.diagenode.com/img/categories/antibodies/histone-marks-illustration.png" /></p>
<p>Diagenode is proud to offer a large range of antibodies against histones and histone modifications. Our antibodies are highly specific and have been validated in many applications, including <strong>ChIP</strong> and <strong>ChIP-seq</strong>.</p>
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<li><strong>Histone H2B and H2B</strong> <strong>modifications </strong>(serine phosphorylation, lysine acetylation)</li>
<li><strong>Histone H3 and H3 modifications </strong>(lysine methylation (mono-, di- and tri-methylated), lysine acetylation, serine phosphorylation, threonine phosphorylation, arginine methylation (mono-methylated, symmetrically and asymmetrically di-methylated))</li>
<li><strong>Histone H4 and H4 modifications (</strong>lysine methylation (mono-, di- and tri-methylated), lysine acetylation, arginine methylation (mono-methylated and symmetrically di-methylated), serine phosphorylation )</li>
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<p><span style="font-weight: 400;"><strong>HDAC's HAT's, HMT's and other</strong> <strong>enzymes</strong> which modify histones can be found in the category <a href="../categories/chromatin-modifying-proteins-histone-transferase">Histone modifying enzymes</a><br /></span></p>
<p><span style="font-weight: 400;"> Diagenode’s highly validated antibodies:</span></p>
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<li><span style="font-weight: 400;"> Highly sensitive and specific</span></li>
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<li><span style="font-weight: 400;"> Batch-specific data is available on the website</span></li>
<li><span style="font-weight: 400;"> Expert technical support</span></li>
<li><span style="font-weight: 400;"> Sample sizes available</span></li>
<li><span style="font-weight: 400;"> 100% satisfaction guarantee</span></li>
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<p><strong>ChIP-seq profile</strong> of active (H3K4me3 and H3K36me3) and inactive (H3K27me3) marks using Diagenode antibodies.</p>
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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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'price_GBP' => '105',
'price_JPY' => '17230',
'price_CNY' => '',
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'country' => 'ALL',
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'quote' => false,
'in_stock' => false,
'featured' => false,
'no_promo' => false,
'online' => true,
'master' => false,
'last_datasheet_update' => '',
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'meta_title' => '',
'meta_keywords' => '',
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'modified' => '2022-01-05 14:55:19',
'created' => '2020-10-29 14:13:54',
'ProductsGroup' => array(
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)
)
$pro = array(
'id' => '3125',
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'description' => '',
'label1' => '',
'info1' => '',
'label2' => '',
'info2' => '',
'label3' => '',
'info3' => '',
'format' => '10 µg',
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'search_order' => '03-Antibody',
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'price_GBP' => '105',
'price_JPY' => '17230',
'price_CNY' => '',
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'country' => 'ALL',
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'in_stock' => false,
'featured' => false,
'no_promo' => false,
'online' => true,
'master' => false,
'last_datasheet_update' => '',
'slug' => 'macroh2a1-monoclonal-antibody-10',
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'meta_keywords' => '',
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'modified' => '2022-01-05 14:55:19',
'created' => '2020-10-29 14:13:54',
'ProductsGroup' => array(
'id' => '343',
'product_id' => '3125',
'group_id' => '305'
)
)
$edit = ''
$testimonials = ''
$featured_testimonials = ''
$related_products = ''
$rrbs_service = array(
(int) 0 => (int) 1894,
(int) 1 => (int) 1895
)
$chipseq_service = array(
(int) 0 => (int) 2683,
(int) 1 => (int) 1835,
(int) 2 => (int) 1836,
(int) 3 => (int) 2684,
(int) 4 => (int) 1838,
(int) 5 => (int) 1839,
(int) 6 => (int) 1856
)
$labelize = object(Closure) {
}
$old_catalog_number = ''
$country_code = 'US'
$other_format = array(
'id' => '3125',
'antibody_id' => '600',
'name' => 'macroH2A.1/H2A.2 Antibody (sample size)',
'description' => '',
'label1' => '',
'info1' => '',
'label2' => '',
'info2' => '',
'label3' => '',
'info3' => '',
'format' => '10 µg',
'catalog_number' => 'C15210003-10',
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'sf_code' => 'C15210003-D001-000582',
'type' => 'FRE',
'search_order' => '03-Antibody',
'price_EUR' => '110',
'price_USD' => '120',
'price_GBP' => '105',
'price_JPY' => '17230',
'price_CNY' => '',
'price_AUD' => '300',
'country' => 'ALL',
'except_countries' => 'None',
'quote' => false,
'in_stock' => false,
'featured' => false,
'no_promo' => false,
'online' => true,
'master' => false,
'last_datasheet_update' => '',
'slug' => 'macroh2a1-monoclonal-antibody-10',
'meta_title' => '',
'meta_keywords' => '',
'meta_description' => '',
'modified' => '2022-01-05 14:55:19',
'created' => '2020-10-29 14:13:54',
'ProductsGroup' => array(
'id' => '343',
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'group_id' => '305'
)
)
$img = 'banners/banner-cut_tag-chipmentation-500.jpg'
$label = '<img src="/img/banners/banner-customizer-back.png" alt=""/>'
$application = array(
'id' => '43',
'position' => '10',
'parent_id' => '40',
'name' => 'ChIP-qPCR (ab)',
'description' => '',
'in_footer' => false,
'in_menu' => false,
'online' => true,
'tabular' => true,
'slug' => 'chip-qpcr-antibodies',
'meta_keywords' => 'Chromatin Immunoprecipitation Sequencing,ChIP-Seq,ChIP-seq grade antibodies,DNA purification,qPCR,Shearing of chromatin',
'meta_description' => 'Diagenode offers a wide range of antibodies and technical support for ChIP-qPCR applications',
'meta_title' => 'ChIP Quantitative PCR Antibodies (ChIP-qPCR) | Diagenode',
'modified' => '2016-01-20 11:30:24',
'created' => '2015-10-20 11:45:36',
'ProductsApplication' => array(
'id' => '4599',
'product_id' => '2840',
'application_id' => '43'
)
)
$slugs = array(
(int) 0 => 'chip-qpcr-antibodies'
)
$applications = array(
'id' => '43',
'position' => '10',
'parent_id' => '40',
'name' => 'ChIP-qPCR (ab)',
'description' => '',
'in_footer' => false,
'in_menu' => false,
'online' => true,
'tabular' => true,
'slug' => 'chip-qpcr-antibodies',
'meta_keywords' => 'Chromatin Immunoprecipitation Sequencing,ChIP-Seq,ChIP-seq grade antibodies,DNA purification,qPCR,Shearing of chromatin',
'meta_description' => 'Diagenode offers a wide range of antibodies and technical support for ChIP-qPCR applications',
'meta_title' => 'ChIP Quantitative PCR Antibodies (ChIP-qPCR) | Diagenode',
'modified' => '2016-01-20 11:30:24',
'created' => '2015-10-20 11:45:36',
'locale' => 'zho'
)
$description = ''
$name = 'ChIP-qPCR (ab)'
$document = array(
'id' => '38',
'name' => 'Epigenetic Antibodies Brochure',
'description' => '<p>More than in any other immuoprecipitation assays, quality antibodies are critical tools in many epigenetics experiments. Since 10 years, Diagenode has developed the most stringent quality production available on the market for antibodies exclusively focused on epigenetic uses. All our antibodies have been qualified to work in epigenetic applications.</p>',
'image_id' => null,
'type' => 'Brochure',
'url' => 'files/brochures/Epigenetic_Antibodies_Brochure.pdf',
'slug' => 'epigenetic-antibodies-brochure',
'meta_keywords' => '',
'meta_description' => '',
'modified' => '2016-06-15 11:24:06',
'created' => '2015-07-03 16:05:27',
'ProductsDocument' => array(
'id' => '2231',
'product_id' => '2840',
'document_id' => '38'
)
)
$sds = array(
'id' => '626',
'name' => 'macroH2A.1/H2A.2 antibody SDS BE nl',
'language' => 'nl',
'url' => 'files/SDS/macroH2A1-H2A2/SDS-C15210003-macroH2A_1_H2A_2_Antibody-BE-nl-GHS_2_0.pdf',
'countries' => 'BE',
'modified' => '2020-07-01 16:22:12',
'created' => '2020-07-01 16:22:12',
'ProductsSafetySheet' => array(
'id' => '1161',
'product_id' => '2840',
'safety_sheet_id' => '626'
)
)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
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