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Pseudouridine monoclonal antibody

CUT&Tag grade Abs

ChIP-seq grade Abs

ChIP grade Abs

Negative IgG control

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Catalog Number

Format

Price

C15200247

50 µg

$380.00
Bulk order

Other format

C15200247-10

10 µg

Monoclonal antibody raised in mouse against pseudouridine (psU) conjugated to BSA.

Lot	001
Concentration	1.44 µg/µl
Species reactivity	Human, other (wide range): positive.
Type	Monoclonal
Purity	Protein A purified monoclonal antibody.
Host	Mouse
Storage Conditions	Store at -20°C; for long storage, store at -80°C. Avoid multiple freeze-thaw cycles.
Storage Buffer	PBS containing 0.05% sodium azide.
Precautions	This product is for research use only. Not for use in diagnostic or therapeutic procedures.

Applications	Suggested dilution	References
RIP*	5 µg per IP	Fig 1, 2

^* Please note that the optimal antibody amount per IP should be determined by the end-user. We recommend testing 2-10 µg per IP.

Validation data

A.

B.

Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU
RNA immunoprecipitation (RIP) was performed on 40 µg total RNA isolated from HeLa cells using 5 µg of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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.

Figure 2. RIP using the Diagenode monoclonal antibody directed against psU
RIP assays were performed on 40 µg total RNA from human HeLa cells using the Diagenode antibody against psU (Cat. No. C15200247). A titration of the antibody consisting of 1, 2 and 5 µg per RIP experiment was analysed. IgG (2 µg/IP) was used as negative IP control. QRT-PCR was performed with primers for the 18 and 28s rRNA genes, for the RPL19 and ATP5E mRNA, shown to contain a psU residue and for the MB gene, used as a negative control. Figure 2 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
実験手法
RIP
RIP Read more
資料
Pseudouridine Monoclonal Antibody datasheet DATASHEET
Monoclonal antibody raised in mouse against pseudouridine (psU) conjugated to BSA. Download

出版物

How to properly cite this product in your work

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Using our products in your publication? Let us know!

Dysregulation of pseudouridylation in small RNAs contributes to papillary thyroid carcinoma metastasis
Xi Wang et al.
Background Previous studies have indicated that ψ-modified small RNAs play crucial roles in tumor metastasis. However, the ψ-modified small RNAs during metastasis of PTC are still unclear. Methods We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and in...

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<p>A. <img src="https://www.diagenode.com/img/product/antibodies/c15200247-rna-1.png" alt="RNA immunoprecipitation" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<p><small><strong>Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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><span style="font-weight: 400;">Diagenode&rsquo;s large range of highly validated antibodies includes the antibodies to study RNA modifications. These antibodies have been thoroughly validated for many applications (RIP, WB, IF, ELISA, Dot blot, IP). Check out all of our highly sensitive and specific antibodies for RNA modifications studies below.</span></p>
<p><span style="font-weight: 400;">Diagenode&rsquo;s highly validated antibodies:</span></p>
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<li>Highly sensitive and specific</li>
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<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>
<li>Expert technical support</li>
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<li>100% satisfaction guarantee</li>
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<p>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
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<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Results</h3>
<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Conclusions</h3>
<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</p>',
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<p>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Results</h3>
<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Conclusions</h3>
<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</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

Notice (8): Undefined variable: header [APP/View/Products/view.ctp, line 755]Code Context<!-- BEGIN: REQUEST_FORM MODAL -->
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<div class="small-5 columns">
<p>A. <img src="https://www.diagenode.com/img/product/antibodies/c15200247-rna-1.png" alt="RNA immunoprecipitation" style="display: block; margin-left: auto; margin-right: auto;" /></p>
<p>B. <img src="https://www.diagenode.com/img/product/antibodies/c15200247-rna-2.png" alt="RNA immunoprecipitation" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<div class="small-7 columns">
<p><small><strong>Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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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			'description' => '<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Background</h3>
<p>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Results</h3>
<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
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<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</p>',
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	'authors' => 'Xi Wang et al.',
	'description' => '<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Background</h3>
<p>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Results</h3>
<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Conclusions</h3>
<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</p>',
	'date' => '2024-10-14',
	'pmid' => 'https://link.springer.com/article/10.1186/s12935-024-03482-3',
	'doi' => 'https://doi.org/10.1186/s12935-024-03482-3',
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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

Notice (8): Undefined variable: message [APP/View/Products/view.ctp, line 755]Code Context<!-- BEGIN: REQUEST_FORM MODAL -->
<div id="request_formModal" class="reveal-modal medium" data-reveal aria-labelledby="modalTitle" aria-hidden="true" role="dialog">
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			'description' => '<p>Monoclonal antibody raised in mouse against pseudouridine (psU) conjugated to BSA.</p>',
			'label1' => 'Validation data',
			'info1' => '<div class="row">
<div class="small-5 columns">
<p>A. <img src="https://www.diagenode.com/img/product/antibodies/c15200247-rna-1.png" alt="RNA immunoprecipitation" style="display: block; margin-left: auto; margin-right: auto;" /></p>
<p>B. <img src="https://www.diagenode.com/img/product/antibodies/c15200247-rna-2.png" alt="RNA immunoprecipitation" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<div class="small-7 columns">
<p><small><strong>Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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">
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<p><img src="https://www.diagenode.com/img/product/antibodies/c15200247-rip.png" alt="RIP" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<div class="small-7 columns">
<p><small><strong>Figure 2. RIP using the Diagenode monoclonal antibody directed against psU</strong><br />RIP assays were performed on 40 &micro;g total RNA from human HeLa cells using the Diagenode antibody against psU (Cat. No. C15200247). A titration of the antibody consisting of 1, 2 and 5 &micro;g per RIP experiment was analysed. IgG (2 &micro;g/IP) was used as negative IP control. QRT-PCR was performed with primers for the 18 and 28s rRNA genes, for the RPL19 and ATP5E mRNA, shown to contain a psU residue and for the MB gene, used as a negative control. Figure 2 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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			'description' => 'Pseudouridine (psU) was the first modified base that was identified in RNA. It is mainly present in non-coding RNAs such as tRNA, rRNA, snRNA and snoRNA but was also found in some mRNAs in both yeast and human. The presence of pseudouridine enhances the structural stability of RNA and is thought to affect rRNA processing, translation and pre-mRNA splicing.',
			'clonality' => '',
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<td>5 &micro;g per IP</td>
<td>Fig 1, 2</td>
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<p></p>
<p><small><sup>*</sup> Please note that the optimal antibody amount per IP should be determined by the end-user. We recommend testing 2-10 &micro;g per IP.</small></p>',
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<p><small><strong>Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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. RIP using the Diagenode monoclonal antibody directed against psU</strong><br />RIP assays were performed on 40 &micro;g total RNA from human HeLa cells using the Diagenode antibody against psU (Cat. No. C15200247). A titration of the antibody consisting of 1, 2 and 5 &micro;g per RIP experiment was analysed. IgG (2 &micro;g/IP) was used as negative IP control. QRT-PCR was performed with primers for the 18 and 28s rRNA genes, for the RPL19 and ATP5E mRNA, shown to contain a psU residue and for the MB gene, used as a negative control. Figure 2 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>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
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<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Conclusions</h3>
<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</p>',
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	'authors' => 'Xi Wang et al.',
	'description' => '<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Background</h3>
<p>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Results</h3>
<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Conclusions</h3>
<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</p>',
	'date' => '2024-10-14',
	'pmid' => 'https://link.springer.com/article/10.1186/s12935-024-03482-3',
	'doi' => 'https://doi.org/10.1186/s12935-024-03482-3',
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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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<p><small><strong>Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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. RIP using the Diagenode monoclonal antibody directed against psU</strong><br />RIP assays were performed on 40 &micro;g total RNA from human HeLa cells using the Diagenode antibody against psU (Cat. No. C15200247). A titration of the antibody consisting of 1, 2 and 5 &micro;g per RIP experiment was analysed. IgG (2 &micro;g/IP) was used as negative IP control. QRT-PCR was performed with primers for the 18 and 28s rRNA genes, for the RPL19 and ATP5E mRNA, shown to contain a psU residue and for the MB gene, used as a negative control. Figure 2 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 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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. RIP using the Diagenode monoclonal antibody directed against psU</strong><br />RIP assays were performed on 40 &micro;g total RNA from human HeLa cells using the Diagenode antibody against psU (Cat. No. C15200247). A titration of the antibody consisting of 1, 2 and 5 &micro;g per RIP experiment was analysed. IgG (2 &micro;g/IP) was used as negative IP control. QRT-PCR was performed with primers for the 18 and 28s rRNA genes, for the RPL19 and ATP5E mRNA, shown to contain a psU residue and for the MB gene, used as a negative control. Figure 2 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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		'description' => 'Pseudouridine (psU) was the first modified base that was identified in RNA. It is mainly present in non-coding RNAs such as tRNA, rRNA, snRNA and snoRNA but was also found in some mRNAs in both yeast and human. The presence of pseudouridine enhances the structural stability of RNA and is thought to affect rRNA processing, translation and pre-mRNA splicing.',
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<p><small><sup>*</sup> Please note that the optimal antibody amount per IP should be determined by the end-user. We recommend testing 2-10 &micro;g per IP.</small></p>',
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<p>Monoclonal antibody raised in mouse against pseudouridine (psU) conjugated to BSA.</p>',
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<p>A. <img src="https://www.diagenode.com/img/product/antibodies/c15200247-rna-1.png" alt="RNA immunoprecipitation" style="display: block; margin-left: auto; margin-right: auto;" /></p>
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<p><small><strong>Figure 1. RNA immunoprecipitation using the Diagenode monoclonal antibody directed against psU</strong><br />RNA immunoprecipitation (RIP) was performed on 40 &micro;g total RNA isolated from HeLa cells using 5 &micro;g of the Diagenode monoclonal antibody against psU (Cat. No. C15200247) or with an equal amount of mouse IgG, used as a negative control. The immunoprecipitated RNA was subsequently analysed on a Bioanalyzer. Figure 1A shows the Bioanalyzer profile obtained with the psU antibody (right) The left panel shows the input. Figure 1B shows the gel image for the psU antibody, the IgG negative control 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. RIP using the Diagenode monoclonal antibody directed against psU</strong><br />RIP assays were performed on 40 &micro;g total RNA from human HeLa cells using the Diagenode antibody against psU (Cat. No. C15200247). A titration of the antibody consisting of 1, 2 and 5 &micro;g per RIP experiment was analysed. IgG (2 &micro;g/IP) was used as negative IP control. QRT-PCR was performed with primers for the 18 and 28s rRNA genes, for the RPL19 and ATP5E mRNA, shown to contain a psU residue and for the MB gene, used as a negative control. Figure 2 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>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
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<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
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	'sf_code' => 'C15200247-D001-000582',
	'type' => 'FRE',
	'search_order' => '03-Antibody',
	'price_EUR' => '105',
	'price_USD' => '115',
	'price_GBP' => '100',
	'price_JPY' => '16450',
	'price_CNY' => '0',
	'price_AUD' => '288',
	'country' => 'ALL',
	'except_countries' => 'None',
	'quote' => false,
	'in_stock' => false,
	'featured' => false,
	'no_promo' => false,
	'online' => true,
	'master' => false,
	'last_datasheet_update' => '',
	'slug' => 'pseudouridine-monoclonal-antibody-10-ug',
	'meta_title' => 'Pseudouridine Monoclonal Antibody | Diagenode',
	'meta_keywords' => '',
	'meta_description' => 'Pseudouridine (psU) Monoclonal Antibody  validated  in RIP.  Batch-specific data available on the website. Sample size available',
	'modified' => '2022-01-05 16:17:23',
	'created' => '2019-03-19 15:29:12',
	'ProductsGroup' => array(
		'id' => '296',
		'product_id' => '3020',
		'group_id' => '261'
	)
)
$img = 'banners/banner-cut_tag-chipmentation-500.jpg'
$label = '<img src="/img/banners/banner-customizer-back.png" alt=""/>'
$application = array(
	'id' => '36',
	'position' => '10',
	'parent_id' => '40',
	'name' => 'RIP',
	'description' => '<p>RIP</p>',
	'in_footer' => false,
	'in_menu' => false,
	'online' => true,
	'tabular' => true,
	'slug' => 'rip',
	'meta_keywords' => 'RIP antibodies,classic monoclonal antibodies,Ago (Argonautes) monoclonal antibody,Snf2h monoclonal antibody - Classic,Diagenode',
	'meta_description' => 'Diagenode offers a wide range of classic monoclonal RIP antibodies.',
	'meta_title' => 'RIP antibodies | Diagenode',
	'modified' => '2016-01-21 08:09:31',
	'created' => '2015-07-08 13:54:45',
	'ProductsApplication' => array(
		'id' => '5017',
		'product_id' => '3019',
		'application_id' => '36'
	)
)
$slugs = array(
	(int) 0 => 'rip'
)
$applications = array(
	'id' => '36',
	'position' => '10',
	'parent_id' => '40',
	'name' => 'RIP',
	'description' => '<p>RIP</p>',
	'in_footer' => false,
	'in_menu' => false,
	'online' => true,
	'tabular' => true,
	'slug' => 'rip',
	'meta_keywords' => 'RIP antibodies,classic monoclonal antibodies,Ago (Argonautes) monoclonal antibody,Snf2h monoclonal antibody - Classic,Diagenode',
	'meta_description' => 'Diagenode offers a wide range of classic monoclonal RIP antibodies.',
	'meta_title' => 'RIP antibodies | Diagenode',
	'modified' => '2016-01-21 08:09:31',
	'created' => '2015-07-08 13:54:45',
	'locale' => 'jpn'
)
$description = '<p>RIP</p>'
$name = 'RIP'
$document = array(
	'id' => '1046',
	'name' => 'Pseudouridine Monoclonal Antibody datasheet',
	'description' => '<p>Monoclonal antibody raised in mouse against pseudouridine (psU) conjugated to BSA.</p>',
	'image_id' => null,
	'type' => 'Datasheet',
	'url' => 'files/products/antibodies/pseudouridine-monoclonal-antibody-50-ug.pdf',
	'slug' => 'pseudouridine-monoclonal-antibody-datasheet',
	'meta_keywords' => '',
	'meta_description' => '',
	'modified' => '2019-03-19 15:40:27',
	'created' => '2019-03-19 15:40:27',
	'ProductsDocument' => array(
		'id' => '2747',
		'product_id' => '3019',
		'document_id' => '1046'
	)
)
$sds = array(
	'id' => '1580',
	'name' => 'Pseudouridine antibody SDS ES es',
	'language' => 'es',
	'url' => 'files/SDS/Pseudouridine/SDS-C15200247-Pseudouridine_Antibody-ES-es-GHS_2_0.pdf',
	'countries' => 'ES',
	'modified' => '2021-08-30 16:57:10',
	'created' => '2021-08-30 16:57:10',
	'ProductsSafetySheet' => array(
		'id' => '2750',
		'product_id' => '3019',
		'safety_sheet_id' => '1580'
	)
)
$publication = array(
	'id' => '4988',
	'name' => 'Dysregulation of pseudouridylation in small RNAs contributes to papillary thyroid carcinoma metastasis',
	'authors' => 'Xi Wang et al.',
	'description' => '<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Background</h3>
<p>Previous studies have indicated that &psi;-modified small RNAs play crucial roles in tumor metastasis. However, the &psi;-modified small RNAs during metastasis of PTC are still unclear.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Methods</h3>
<p>We compared the pseudouridine synthase 7 (PUS7) alteration between metastatic and non-metastatic PTCs, and investigated its correlation with clinicopathological features. Additionally, we employed a small RNA &psi; modification microarray to examine the small RNA &psi; modification profile in both metastatic and non-metastatic PTCs, as well as paired paracancerous tissues. The key molecule involved in &psi; modification, pre-miR-8082, was identified and found to regulate the expression of CD47. Experiments in vitro were conducted to further investigate the function of PUS7 and CD47 in PTC.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Results</h3>
<p>Our results demonstrated that PUS7 was down-regulated in PTC and was closely associated with metastasis. Moreover, the &psi; modification of pre-miR-8082 was found to be decreased, resulting in down-expression of pre-miR-8082 and miR-8082, leading to the loss of the inhibitory effect on CD47, thereby promoting tumor migration.</p>
<h3 class="c-article__sub-heading" data-test="abstract-sub-heading">Conclusions</h3>
<p>Our study demonstrates that PUS7 promotes the inhibition of CD47 and inhibits metastasis of PTC cells by regulating the &psi; modification of pre-miR-8082. These results suggest that PUS7 and &psi; pre-miR-8082 may serve as potential targets and diagnostic markers for PTC metastasis.</p>',
	'date' => '2024-10-14',
	'pmid' => 'https://link.springer.com/article/10.1186/s12935-024-03482-3',
	'doi' => 'https://doi.org/10.1186/s12935-024-03482-3',
	'modified' => '2024-10-18 11:41:05',
	'created' => '2024-10-18 11:41:05',
	'ProductsPublication' => array(
		'id' => '7592',
		'product_id' => '3019',
		'publication_id' => '4988'
	)
)
$externalLink = ' <a href="https://link.springer.com/article/10.1186/s12935-024-03482-3" target="_blank"><i class="fa fa-external-link"></i></a>'
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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