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<p><small><strong>Figure 1. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from NIH3T3 using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The antibody was used at different dilutions. The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from HeLa, 293T, NIH-3T3, Rat1, BHK-21 and CV-1 cells (lanes 1-6, respectively) using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 3. IP using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />IP was performed on whole cell extracts (300 µg) from HeLa cells ectopically expressing Flag-tagged lamin A using 5 µg of the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The immunoprecipitated proteins were subsequently analysed by Western blot with the Lamin A/C antibody as described above. Lane 3 shows the result of the IP, the input (15 µg) is shown in lane 1, lane 2 shows the cell lysate after the IP.</small></p>
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<p><small><strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />HeLa cells ectopically expressing Flag-tagged lamin A were fixed with 3.7% formaldehyde, permeabilized in 0,5% Triton X-100 and blocked in TBS containing 2% BSA. The cells were stained with the Lamin A/C antibody diluted 1:1,000 for 2 hours at RT, followed by incubation with an anti mouse secondary antibody coupled to AF596 for 1 h at RT (middle). Nuclei were counter-stained with Hoechst 33342 (left). A merge of the two stainings is shown on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from HeLa, 293T, NIH-3T3, Rat1, BHK-21 and CV-1 cells (lanes 1-6, respectively) using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />HeLa cells ectopically expressing Flag-tagged lamin A were fixed with 3.7% formaldehyde, permeabilized in 0,5% Triton X-100 and blocked in TBS containing 2% BSA. The cells were stained with the Lamin A/C antibody diluted 1:1,000 for 2 hours at RT, followed by incubation with an anti mouse secondary antibody coupled to AF596 for 1 h at RT (middle). Nuclei were counter-stained with Hoechst 33342 (left). A merge of the two stainings is shown on the right.</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>
<h5><sup>Check our selection of antibodies validated in IF.</sup></h5>',
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<p><small><strong>Figure 1. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from NIH3T3 using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The antibody was used at different dilutions. The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from HeLa, 293T, NIH-3T3, Rat1, BHK-21 and CV-1 cells (lanes 1-6, respectively) using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 3. IP using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />IP was performed on whole cell extracts (300 µg) from HeLa cells ectopically expressing Flag-tagged lamin A using 5 µg of the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The immunoprecipitated proteins were subsequently analysed by Western blot with the Lamin A/C antibody as described above. Lane 3 shows the result of the IP, the input (15 µg) is shown in lane 1, lane 2 shows the cell lysate after the IP.</small></p>
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<p><small><strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />HeLa cells ectopically expressing Flag-tagged lamin A were fixed with 3.7% formaldehyde, permeabilized in 0,5% Triton X-100 and blocked in TBS containing 2% BSA. The cells were stained with the Lamin A/C antibody diluted 1:1,000 for 2 hours at RT, followed by incubation with an anti mouse secondary antibody coupled to AF596 for 1 h at RT (middle). Nuclei were counter-stained with Hoechst 33342 (left). A merge of the two stainings is shown on the right.</small></p>
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Dispatcher::dispatch() - CORE/Cake/Routing/Dispatcher.php, line 167
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<p><small><strong>Figure 1. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from NIH3T3 using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The antibody was used at different dilutions. The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from HeLa, 293T, NIH-3T3, Rat1, BHK-21 and CV-1 cells (lanes 1-6, respectively) using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 3. IP using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />IP was performed on whole cell extracts (300 µg) from HeLa cells ectopically expressing Flag-tagged lamin A using 5 µg of the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The immunoprecipitated proteins were subsequently analysed by Western blot with the Lamin A/C antibody as described above. Lane 3 shows the result of the IP, the input (15 µg) is shown in lane 1, lane 2 shows the cell lysate after the IP.</small></p>
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<p><small><strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />HeLa cells ectopically expressing Flag-tagged lamin A were fixed with 3.7% formaldehyde, permeabilized in 0,5% Triton X-100 and blocked in TBS containing 2% BSA. The cells were stained with the Lamin A/C antibody diluted 1:1,000 for 2 hours at RT, followed by incubation with an anti mouse secondary antibody coupled to AF596 for 1 h at RT (middle). Nuclei were counter-stained with Hoechst 33342 (left). A merge of the two stainings is shown on the right.</small></p>
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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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<p><small><strong>Figure 1. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from NIH3T3 using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The antibody was used at different dilutions. The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 2. Western blot analysis using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />Western blot was performed on protein extracts from HeLa, 293T, NIH-3T3, Rat1, BHK-21 and CV-1 cells (lanes 1-6, respectively) using the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The marker is shown on the left, the position of Lamin A and Lamin C is indicated on the right.</small></p>
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<p><small><strong>Figure 3. IP using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />IP was performed on whole cell extracts (300 µg) from HeLa cells ectopically expressing Flag-tagged lamin A using 5 µg of the Diagenode antibody against Lamin A/C (Cat. No. C15200243). The immunoprecipitated proteins were subsequently analysed by Western blot with the Lamin A/C antibody as described above. Lane 3 shows the result of the IP, the input (15 µg) is shown in lane 1, lane 2 shows the cell lysate after the IP.</small></p>
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<p><small><strong>Figure 4. Immunofluorescence using the Diagenode monoclonal antibody directed against Lamin A/C</strong><br />HeLa cells ectopically expressing Flag-tagged lamin A were fixed with 3.7% formaldehyde, permeabilized in 0,5% Triton X-100 and blocked in TBS containing 2% BSA. The cells were stained with the Lamin A/C antibody diluted 1:1,000 for 2 hours at RT, followed by incubation with an anti mouse secondary antibody coupled to AF596 for 1 h at RT (middle). Nuclei were counter-stained with Hoechst 33342 (left). A merge of the two stainings is shown on the right.</small></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>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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<li><strong>Focused</strong> - Diagenode's selection of antibodies is exclusively dedicated for epigenetic research. <a title="See the full collection." href="../categories/all-antibodies">See the full collection.</a></li>
<li><strong>Strict quality standards</strong> with rigorous QC and validation</li>
<li><strong>Classified</strong> based on level of validation for flexibility of application</li>
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<p>Existing sample sizes are listed below. We will soon expand our collection. Are you looking for a sample size of another antibody? Just <a href="mailto:agnieszka.zelisko@diagenode.com?Subject=Sample%20Size%20Request" target="_top">Contact us</a>.</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
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