IGF2BP1 polyclonal antibody

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			'name' => 'IGF2BP1 polyclonal antibody',
			'description' => '<p><strong>Other names:</strong> CRD-BP, VICKZ1, IMP-1, CRDBP, ZBP-1, IMP1, ZBP1</p>
<p>Polyclonal antibody raised in rabbit against human IGF2BP1 (Insulin Like Growth Factor 2 mRNA Binding Protein 1), using KLH-conjugated synthetic peptide from the C-teminal part of the protein.</p>',
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<div class="small-5 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410349-rip.jpg" alt="ChIP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410349-rip-2.jpg" alt="RIP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<p><small><strong>Figure 1. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on total RNA isolated from 10 million K562 cells using 15 &micro;g of the Diagenode antibody against IGF2BP1 (Cat. No. C15410349) or with an equal amount of rabbit IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1 shows the Bioanalyzer profile obtained with the negative control (upper left) and the IGF2BP1 antibody (upper right). The lower figure shows the gel image for the negative IgG control, the IGF2BP1 antibody and the input (lane 1, 2 and 3 respectively). The marker (in bp) is shown on the left, the position of the 28s and 18s ribosomal RNA is indicated on the right.</small></p>
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<p><img src="https://www.diagenode.com/img/product/antibodies/C15410349-wb.jpg" alt="WB" style="display: block; margin-left: auto; margin-right: auto;" /></p>
</div>
<div class="small-7 columns">
<p><small><strong>Figure 2. Western blot analysis using the Diagenode antibody directed against IGF2BP1</strong><br />Whole cell extracts from K562, 293T, HeLa and Jurkat cells (lanes 1, 2, 3 and 4, respectively) were analysed by Western blot using the Diagenode antibody against IGF2BP1 (<span>Cat</span>. No. C15410349) diluted 1:1,000 in TBS containing 1% 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/C15410349-ip.jpg" alt="IP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
</div>
<div class="small-7 columns">
<p><small><strong>Figure 3. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on whole cell extracts from K562 cells using 5 &micro;g of the Diagenode monoclonal antibody against IGF2BP1 (<span>Cat</span>. No. C15410349, lane 2). An equal amount of rabbit IgG was used as a negative control (lane 1). The immunoprecipitated IGF2BP1 protein was subsequently detected by western blot with the IGF2BP1 antibody as described above.</small></p>
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<th>Suggested dilution</th>
<th>References</th>
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<td>RIP</td>
<td>15 &micro;g per 10<sup>7</sup> cells</td>
<td>Fig 1</td>
</tr>
<tr>
<td>Western blotting</td>
<td>1:1,000</td>
<td>Fig 2</td>
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<tr>
<td>IP</td>
<td>5 &micro;g per 2.5x10<sup>6</sup> cells</td>
<td>Fig 3</td>
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		'description' => '<p><strong>Other names:</strong> CRD-BP, VICKZ1, IMP-1, CRDBP, ZBP-1, IMP1, ZBP1</p>
<p>Polyclonal antibody raised in rabbit against human IGF2BP1 (Insulin Like Growth Factor 2 mRNA Binding Protein 1), using KLH-conjugated synthetic peptide from the C-teminal part of the protein.</p>',
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<div class="small-5 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410349-rip.jpg" alt="ChIP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410349-rip-2.jpg" alt="RIP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<p><small><strong>Figure 1. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on total RNA isolated from 10 million K562 cells using 15 &micro;g of the Diagenode antibody against IGF2BP1 (Cat. No. C15410349) or with an equal amount of rabbit IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1 shows the Bioanalyzer profile obtained with the negative control (upper left) and the IGF2BP1 antibody (upper right). The lower figure shows the gel image for the negative IgG control, the IGF2BP1 antibody and the input (lane 1, 2 and 3 respectively). The marker (in bp) is shown on the left, the position of the 28s and 18s ribosomal RNA is indicated on the right.</small></p>
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<div class="row">
<div class="small-5 columns">
<p><img src="https://www.diagenode.com/img/product/antibodies/C15410349-wb.jpg" alt="WB" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode antibody directed against IGF2BP1</strong><br />Whole cell extracts from K562, 293T, HeLa and Jurkat cells (lanes 1, 2, 3 and 4, respectively) were analysed by Western blot using the Diagenode antibody against IGF2BP1 (<span>Cat</span>. No. C15410349) diluted 1:1,000 in TBS containing 1% 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/C15410349-ip.jpg" alt="IP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
</div>
<div class="small-7 columns">
<p><small><strong>Figure 3. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on whole cell extracts from K562 cells using 5 &micro;g of the Diagenode monoclonal antibody against IGF2BP1 (<span>Cat</span>. No. C15410349, lane 2). An equal amount of rabbit IgG was used as a negative control (lane 1). The immunoprecipitated IGF2BP1 protein was subsequently detected by western blot with the IGF2BP1 antibody as described above.</small></p>
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<th>References</th>
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<td>RIP</td>
<td>15 &micro;g per 10<sup>7</sup> cells</td>
<td>Fig 1</td>
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<td>Western blotting</td>
<td>1:1,000</td>
<td>Fig 2</td>
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<td>IP</td>
<td>5 &micro;g per 2.5x10<sup>6</sup> cells</td>
<td>Fig 3</td>
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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><span style="font-weight: 400;">Diagenode&rsquo;s highly validated antibodies:</span></p>
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include - APP/View/Products/view.ctp, line 755
View::_evaluate() - CORE/Cake/View/View.php, line 971
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 (Notice): Undefined variable: header [APP/View/Products/view.ctp, line 755]
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<p><small><strong>Figure 1. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on total RNA isolated from 10 million K562 cells using 15 &micro;g of the Diagenode antibody against IGF2BP1 (Cat. No. C15410349) or with an equal amount of rabbit IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1 shows the Bioanalyzer profile obtained with the negative control (upper left) and the IGF2BP1 antibody (upper right). The lower figure shows the gel image for the negative IgG control, the IGF2BP1 antibody and the input (lane 1, 2 and 3 respectively). The marker (in bp) is shown on the left, the position of the 28s and 18s ribosomal RNA is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode antibody directed against IGF2BP1</strong><br />Whole cell extracts from K562, 293T, HeLa and Jurkat cells (lanes 1, 2, 3 and 4, respectively) were analysed by Western blot using the Diagenode antibody against IGF2BP1 (<span>Cat</span>. No. C15410349) diluted 1:1,000 in TBS containing 1% 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 3. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on whole cell extracts from K562 cells using 5 &micro;g of the Diagenode monoclonal antibody against IGF2BP1 (<span>Cat</span>. No. C15410349, lane 2). An equal amount of rabbit IgG was used as a negative control (lane 1). The immunoprecipitated IGF2BP1 protein was subsequently detected by western blot with the IGF2BP1 antibody as described above.</small></p>
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include - APP/View/Products/view.ctp, line 755
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 (Notice): Undefined variable: message [APP/View/Products/view.ctp, line 755]
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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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include - APP/View/Products/view.ctp, line 755
View::_evaluate() - CORE/Cake/View/View.php, line 971
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 (Notice): Undefined variable: campaign_id [APP/View/Products/view.ctp, line 755]
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<p>Polyclonal antibody raised in rabbit against human IGF2BP1 (Insulin Like Growth Factor 2 mRNA Binding Protein 1), using KLH-conjugated synthetic peptide from the C-teminal part of the protein.</p>',
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<p><small><strong>Figure 1. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on total RNA isolated from 10 million K562 cells using 15 &micro;g of the Diagenode antibody against IGF2BP1 (Cat. No. C15410349) or with an equal amount of rabbit IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1 shows the Bioanalyzer profile obtained with the negative control (upper left) and the IGF2BP1 antibody (upper right). The lower figure shows the gel image for the negative IgG control, the IGF2BP1 antibody and the input (lane 1, 2 and 3 respectively). The marker (in bp) is shown on the left, the position of the 28s and 18s ribosomal RNA is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode antibody directed against IGF2BP1</strong><br />Whole cell extracts from K562, 293T, HeLa and Jurkat cells (lanes 1, 2, 3 and 4, respectively) were analysed by Western blot using the Diagenode antibody against IGF2BP1 (<span>Cat</span>. No. C15410349) diluted 1:1,000 in TBS containing 1% 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 3. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on whole cell extracts from K562 cells using 5 &micro;g of the Diagenode monoclonal antibody against IGF2BP1 (<span>Cat</span>. No. C15410349, lane 2). An equal amount of rabbit IgG was used as a negative control (lane 1). The immunoprecipitated IGF2BP1 protein was subsequently detected by western blot with the IGF2BP1 antibody as described above.</small></p>
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			'application_table' => '<table>
<thead>
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<th>Suggested dilution</th>
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<td>RIP</td>
<td>15 &micro;g per 10<sup>7</sup> cells</td>
<td>Fig 1</td>
</tr>
<tr>
<td>Western blotting</td>
<td>1:1,000</td>
<td>Fig 2</td>
</tr>
<tr>
<td>IP</td>
<td>5 &micro;g per 2.5x10<sup>6</sup> cells</td>
<td>Fig 3</td>
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</table>',
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<div class="small-5 columns">
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<p><small><strong>Figure 1. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on total RNA isolated from 10 million K562 cells using 15 &micro;g of the Diagenode antibody against IGF2BP1 (Cat. No. C15410349) or with an equal amount of rabbit IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1 shows the Bioanalyzer profile obtained with the negative control (upper left) and the IGF2BP1 antibody (upper right). The lower figure shows the gel image for the negative IgG control, the IGF2BP1 antibody and the input (lane 1, 2 and 3 respectively). The marker (in bp) is shown on the left, the position of the 28s and 18s ribosomal RNA is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode antibody directed against IGF2BP1</strong><br />Whole cell extracts from K562, 293T, HeLa and Jurkat cells (lanes 1, 2, 3 and 4, respectively) were analysed by Western blot using the Diagenode antibody against IGF2BP1 (<span>Cat</span>. No. C15410349) diluted 1:1,000 in TBS containing 1% 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 3. Immunoprecipitation using the Diagenode antibody directed against IGF2BP1</strong><br />Immunoprecipitation was performed on whole cell extracts from K562 cells using 5 &micro;g of the Diagenode monoclonal antibody against IGF2BP1 (<span>Cat</span>. No. C15410349, lane 2). An equal amount of rabbit IgG was used as a negative control (lane 1). The immunoprecipitated IGF2BP1 protein was subsequently detected by western blot with the IGF2BP1 antibody as described above.</small></p>
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		'search_order' => '03-Antibody',
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		'meta_title' => 'IGF2BP1 Polyclonal Antibody | Diagenode',
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		'meta_description' => 'IGF2BP1 (Insulin Like Growth Factor 2 mRNA Binding Protein 1) Polyclonal Antibody validated  in IP, RIP and WB. Batch-specific data available on the website. Other names: CRD-BP, VICKZ1, IMP-1, CRDBP, ZBP-1, IMP1, ZBP1',
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		'name' => 'IGF2BP1 polyclonal antibody',
		'description' => 'IGF2BP1 (UniProtKB/Swiss-Prot entry Q9NZI8) is a member of the insulin-like growth factor 2 mRNA-binding protein family. It binds to the mRNAs of certain genes, including insulin-like growth factor 2, beta-actin and beta-transducin repeat-containing protein, thereby regulating translation.',
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		'isotype' => '',
		'lot' => '001',
		'concentration' => '1 μg/μl',
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		'type' => 'Polyclonal',
		'purity' => 'Affinity purified polyclonal antibody.',
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		'application_table' => '<table>
<thead>
<tr>
<th>Applications</th>
<th>Suggested dilution</th>
<th>References</th>
</tr>
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<tbody>
<tr>
<td>RIP</td>
<td>15 &micro;g per 10<sup>7</sup> cells</td>
<td>Fig 1</td>
</tr>
<tr>
<td>Western blotting</td>
<td>1:1,000</td>
<td>Fig 2</td>
</tr>
<tr>
<td>IP</td>
<td>5 &micro;g per 2.5x10<sup>6</sup> cells</td>
<td>Fig 3</td>
</tr>
</tbody>
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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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			'description' => '<p><span style="font-weight: 400;">All Diagenode&rsquo;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&rsquo;s highly validated antibodies:</span></p>
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<li>Cost-effective (requires less antibody per reaction)</li>
<li>Batch-specific data is available on the website</li>
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			'meta_description' => 'Diagenode Offers Strict quality standards with Rigorous QC and validated Antibodies. Classified based on level of validation for flexibility of Application. Comprehensive selection of histone and non-histone Antibodies',
			'meta_title' => 'Diagenode's selection of Antibodies is exclusively dedicated for Epigenetic Research | Diagenode',
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<li>Batch-specific data is available on the website</li>
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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 1055
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