| DiaMag anti-mouse IgG-coated magnetic beads DATASHEET These magnetic beads coated with anti-mouse IgG antibody have been extensively validated in chrom... | Download |
These magnetic beads coated with anti-mouse IgG antibody have been extensively validated in chromatin immunoprecipitation assay (ChIP) and methylated DNA immunoprecipitation assays (MeDIP). The beads bind mouse IgG1, IgG2a, IgG2b. The beads should be washed before use.
| DiaMag anti-mouse IgG-coated magnetic beads DATASHEET These magnetic beads coated with anti-mouse IgG antibody have been extensively validated in chrom... | Download |
| DiaMag anti-mouse IgG coated magnetic beads SDS US en | Download |
| DiaMag anti-mouse IgG coated magnetic beads SDS GB en | Download |
| DiaMag anti-mouse IgG coated magnetic beads SDS BE fr | Download |
| DiaMag anti-mouse IgG coated magnetic beads SDS FR fr | Download |
| DiaMag anti-mouse IgG coated magnetic beads SDS ES es | Download |
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Identification of a PadR-type regulator essential for intracellularpathogenesis of |
Formation of the CenH3-Deficient Holocentromere in Lepidoptera AvoidsActive Chromatin. |
Novel dual regulators of Pseudomonas aeruginosa essential for productive biofilms and virulence. |
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', 'description' => '<p>Burkholderia pseudomallei (Bp) is the causative agent of melioidosis, a disease endemic to the tropics. Melioidosis manifests in various ways ranging from acute skin lesions to pneumonia and, in rare cases, infection of the central nervous system. Bp is a facultative intracellular pathogen and it can infect various cell types. The Bp intracellular lifecycle has been partially elucidated and is highly complex. Herein, we have identified a transcriptional regulator, BP1026B_II1198, that is differentially expressed as Bp transits through host cells. A deletion mutant of BP1026B_II1198 was attenuated in RAW264.7 cell and BALB/c mouse infection. To further characterize the function of this transcriptional regulator, we endeavored to determine the regulon of BP1026B_II1198. RNA-seq analysis showed the global picture of genes regulated while ChIP-seq analysis identified two specific BP1026B_II1198 binding regions on chromosome II. We investigated the transposon mutants of these genes controlled by BP1026B_II1198 and confirmed that these genes contribute to pathogenesis in RAW264.7 murine macrophage cells. 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Based on reciprocal centromere occupancy patterns observed along differentially expressed orthologous genes of Lepidoptera, we further found that holocentromere formation in a manner that is recessive to chromatin dynamics is evolutionarily conserved. Our results help us discuss the plasticity of centromeres in the context of a role for the chromosome-wide chromatin landscape in conferring centromere identity rather than the presence of CenH3. Given the co-occurrence of CenH3 loss and holocentricity in insects, we further propose that the evolutionary establishment of holocentromeres in insects was facilitated through the loss of a CenH3-specified centromere.</p>', 'date' => '2020-10-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/33125865', 'doi' => '10.1016/j.cub.2020.09.078', 'modified' => '2021-03-17 17:13:50', 'created' => '2021-02-18 10:21:53', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 2 => array( 'id' => '3598', 'name' => 'Novel dual regulators of Pseudomonas aeruginosa essential for productive biofilms and virulence.', 'authors' => 'Heacock-Kang Y, Zarzycki-Siek J, Sun Z, Poonsuk K, Bluhm AP, Cabanas D, Fogen D, McMillan IA, Chuanchuen R, Hoang TT', 'description' => '<p>Gene regulation network in Pseudomonas aeruginosa is complex. With a relatively large genome (6.2 Mb), there is a significant portion of genes that are proven or predicted to be transcriptional regulators. 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PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. 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Attempts to confirm the binding sequences by electrophoretic mobility shift assay led to the discovery of a co-regulator, PA1413, via co-immunoprecipitation assay. PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. 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', 'description' => '<p>Burkholderia pseudomallei (Bp) is the causative agent of melioidosis, a disease endemic to the tropics. Melioidosis manifests in various ways ranging from acute skin lesions to pneumonia and, in rare cases, infection of the central nervous system. Bp is a facultative intracellular pathogen and it can infect various cell types. The Bp intracellular lifecycle has been partially elucidated and is highly complex. Herein, we have identified a transcriptional regulator, BP1026B_II1198, that is differentially expressed as Bp transits through host cells. A deletion mutant of BP1026B_II1198 was attenuated in RAW264.7 cell and BALB/c mouse infection. To further characterize the function of this transcriptional regulator, we endeavored to determine the regulon of BP1026B_II1198. RNA-seq analysis showed the global picture of genes regulated while ChIP-seq analysis identified two specific BP1026B_II1198 binding regions on chromosome II. We investigated the transposon mutants of these genes controlled by BP1026B_II1198 and confirmed that these genes contribute to pathogenesis in RAW264.7 murine macrophage cells. Taken together, the data presented here shed light on the regulon of BP1026B_II1198 and its role during intracellular infection and highlights an integral portion of the highly complex regulation network of Bp during host infection.</p>', 'date' => '2021-05-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/34001967', 'doi' => '10.1038/s41598-021-89852-7', 'modified' => '2022-08-02 16:55:52', 'created' => '2022-05-19 10:41:50', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 1 => array( 'id' => '4092', 'name' => 'Formation of the CenH3-Deficient Holocentromere in Lepidoptera AvoidsActive Chromatin.', 'authors' => 'Senaratne, Aruni P and Muller, Héloïse and Fryer, Kelsey A and Kawamoto,Munetaka and Katsuma, Susumu and Drinnenberg, Ines A', 'description' => '<p>Despite the essentiality for faithful chromosome segregation, centromere architectures are diverse among eukaryotes and embody two main configurations: mono- and holocentromeres, referring, respectively, to localized or unrestricted distribution of centromeric activity. Of the two, some holocentromeres offer the curious condition of having arisen independently in multiple insects, most of which have lost the otherwise essential centromere-specifying factor CenH3 (first described as CENP-A in humans). The loss of CenH3 raises intuitive questions about how holocentromeres are organized and regulated in CenH3-lacking insects. Here, we report the first chromatin-level description of CenH3-deficient holocentromeres by leveraging recently identified centromere components and genomics approaches to map and characterize the holocentromeres of the silk moth Bombyx mori, a representative lepidopteran insect lacking CenH3. This uncovered a robust correlation between the distribution of centromere sites and regions of low chromatin activity along B. mori chromosomes. Transcriptional perturbation experiments recapitulated the exclusion of B. mori centromeres from active chromatin. Based on reciprocal centromere occupancy patterns observed along differentially expressed orthologous genes of Lepidoptera, we further found that holocentromere formation in a manner that is recessive to chromatin dynamics is evolutionarily conserved. Our results help us discuss the plasticity of centromeres in the context of a role for the chromosome-wide chromatin landscape in conferring centromere identity rather than the presence of CenH3. Given the co-occurrence of CenH3 loss and holocentricity in insects, we further propose that the evolutionary establishment of holocentromeres in insects was facilitated through the loss of a CenH3-specified centromere.</p>', 'date' => '2020-10-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/33125865', 'doi' => '10.1016/j.cub.2020.09.078', 'modified' => '2021-03-17 17:13:50', 'created' => '2021-02-18 10:21:53', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 2 => array( 'id' => '3598', 'name' => 'Novel dual regulators of Pseudomonas aeruginosa essential for productive biofilms and virulence.', 'authors' => 'Heacock-Kang Y, Zarzycki-Siek J, Sun Z, Poonsuk K, Bluhm AP, Cabanas D, Fogen D, McMillan IA, Chuanchuen R, Hoang TT', 'description' => '<p>Gene regulation network in Pseudomonas aeruginosa is complex. With a relatively large genome (6.2 Mb), there is a significant portion of genes that are proven or predicted to be transcriptional regulators. Many of these regulators have been shown to play important roles in biofilm formation and maintenance. In this study, we present a novel transcriptional regulator, PA1226, which modulates biofilm formation and virulence in P. aeruginosa. Mutation in the gene encoding this regulator abolished the ability of P. aeruginosa to produce biofilms in vitro, without any effect on the planktonic growth. This regulator is also essential for the in vivo fitness and pathogenesis in both Drosophila melanogaster and BALB/c mouse lung infection models. Transcriptome analysis revealed that PA1226 regulates many essential virulence genes/pathways, including those involved in alginate, pili, and LPS biosynthesis. Genes/operons directly regulated by PA1226 and potential binding sequences were identified via ChIP-seq. Attempts to confirm the binding sequences by electrophoretic mobility shift assay led to the discovery of a co-regulator, PA1413, via co-immunoprecipitation assay. PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. A model is proposed, summarizing our finding on this novel dual-regulation system.</p>', 'date' => '2018-08-01', 'pmid' => 'http://www.pubmed.gov/29995308', 'doi' => '10.1111/mmi.14063', 'modified' => '2019-04-17 15:07:51', 'created' => '2019-04-16 12:25:30', 'ProductsPublication' => array( [maximum depth reached] ) ) ), 'Testimonial' => array(), 'Area' => array(), 'SafetySheet' => array( (int) 0 => array( 'id' => '336', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS US en', 'language' => 'en', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-US-en-GHS_1_0.pdf', 'countries' => 'US', 'modified' => '2020-06-09 13:03:27', 'created' => '2020-06-09 13:03:27', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 1 => array( 'id' => '334', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS GB en', 'language' => 'en', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-GB-en-GHS_1_0.pdf', 'countries' => 'GB', 'modified' => '2020-06-09 13:01:35', 'created' => '2020-06-09 13:01:35', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 2 => array( 'id' => '329', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS BE fr', 'language' => 'fr', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-BE-fr-GHS_1_0.pdf', 'countries' => 'BE', 'modified' => '2020-06-09 12:58:49', 'created' => '2020-06-09 12:58:49', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 3 => array( 'id' => '333', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS FR fr', 'language' => 'fr', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-FR-fr-GHS_1_0.pdf', 'countries' => 'FR', 'modified' => '2020-06-09 13:00:53', 'created' => '2020-06-09 13:00:53', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 4 => array( 'id' => '332', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS ES es', 'language' => 'es', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-ES-es-GHS_1_0.pdf', 'countries' => 'ES', 'modified' => '2020-06-09 13:00:23', 'created' => '2020-06-09 13:00:23', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 5 => array( 'id' => '331', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS DE de', 'language' => 'de', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-DE-de-GHS_1_0.pdf', 'countries' => 'DE', 'modified' => '2020-06-09 12:59:50', 'created' => '2020-06-09 12:59:50', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 6 => array( 'id' => '335', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS JP ja', 'language' => 'ja', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-JP-ja-GHS_2_0.pdf', 'countries' => 'JP', 'modified' => '2020-06-09 13:02:44', 'created' => '2020-06-09 13:02:44', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 7 => array( 'id' => '330', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS BE nl', 'language' => 'nl', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-BE-nl-GHS_1_0.pdf', 'countries' => 'BE', 'modified' => '2020-06-09 12:59:19', 'created' => '2020-06-09 12:59:19', 'ProductsSafetySheet' => array( [maximum depth reached] ) ) ) ) $meta_canonical = 'https://www.diagenode.com/jp/p/diamag-anti-mouse-igg-coated-magnetic-beads-220-ul' $country = 'US' $countries_allowed = array( (int) 0 => 'CA', (int) 1 => 'US', (int) 2 => 'IE', (int) 3 => 'GB', (int) 4 => 'DK', (int) 5 => 'NO', (int) 6 => 'SE', (int) 7 => 'FI', (int) 8 => 'NL', (int) 9 => 'BE', (int) 10 => 'LU', (int) 11 => 'FR', (int) 12 => 'DE', (int) 13 => 'CH', (int) 14 => 'AT', (int) 15 => 'ES', (int) 16 => 'IT', (int) 17 => 'PT' ) $outsource = false $other_formats = array( (int) 0 => array( 'id' => '1911', 'antibody_id' => null, 'name' => 'DiaMag anti-mouse IgG coated magnetic beads', 'description' => '<p><span>These magnetic beads coated with anti-mouse IgG antibody have been extensively validated in chromatin immunoprecipitation assay (ChIP) and methylated DNA immunoprecipitation assays (MeDIP). 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With a relatively large genome (6.2 Mb), there is a significant portion of genes that are proven or predicted to be transcriptional regulators. Many of these regulators have been shown to play important roles in biofilm formation and maintenance. In this study, we present a novel transcriptional regulator, PA1226, which modulates biofilm formation and virulence in P. aeruginosa. Mutation in the gene encoding this regulator abolished the ability of P. aeruginosa to produce biofilms in vitro, without any effect on the planktonic growth. This regulator is also essential for the in vivo fitness and pathogenesis in both Drosophila melanogaster and BALB/c mouse lung infection models. Transcriptome analysis revealed that PA1226 regulates many essential virulence genes/pathways, including those involved in alginate, pili, and LPS biosynthesis. Genes/operons directly regulated by PA1226 and potential binding sequences were identified via ChIP-seq. Attempts to confirm the binding sequences by electrophoretic mobility shift assay led to the discovery of a co-regulator, PA1413, via co-immunoprecipitation assay. PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. A model is proposed, summarizing our finding on this novel dual-regulation system.</p>', 'date' => '2018-08-01', 'pmid' => 'http://www.pubmed.gov/29995308', 'doi' => '10.1111/mmi.14063', 'modified' => '2019-04-17 15:07:51', 'created' => '2019-04-16 12:25:30', 'ProductsPublication' => array( 'id' => '3469', 'product_id' => '1910', 'publication_id' => '3598' ) ) $externalLink = ' <a href="http://www.pubmed.gov/29995308" 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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', 'description' => '<p>Burkholderia pseudomallei (Bp) is the causative agent of melioidosis, a disease endemic to the tropics. Melioidosis manifests in various ways ranging from acute skin lesions to pneumonia and, in rare cases, infection of the central nervous system. Bp is a facultative intracellular pathogen and it can infect various cell types. The Bp intracellular lifecycle has been partially elucidated and is highly complex. Herein, we have identified a transcriptional regulator, BP1026B_II1198, that is differentially expressed as Bp transits through host cells. A deletion mutant of BP1026B_II1198 was attenuated in RAW264.7 cell and BALB/c mouse infection. To further characterize the function of this transcriptional regulator, we endeavored to determine the regulon of BP1026B_II1198. RNA-seq analysis showed the global picture of genes regulated while ChIP-seq analysis identified two specific BP1026B_II1198 binding regions on chromosome II. We investigated the transposon mutants of these genes controlled by BP1026B_II1198 and confirmed that these genes contribute to pathogenesis in RAW264.7 murine macrophage cells. Taken together, the data presented here shed light on the regulon of BP1026B_II1198 and its role during intracellular infection and highlights an integral portion of the highly complex regulation network of Bp during host infection.</p>', 'date' => '2021-05-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/34001967', 'doi' => '10.1038/s41598-021-89852-7', 'modified' => '2022-08-02 16:55:52', 'created' => '2022-05-19 10:41:50', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 1 => array( 'id' => '4092', 'name' => 'Formation of the CenH3-Deficient Holocentromere in Lepidoptera AvoidsActive Chromatin.', 'authors' => 'Senaratne, Aruni P and Muller, Héloïse and Fryer, Kelsey A and Kawamoto,Munetaka and Katsuma, Susumu and Drinnenberg, Ines A', 'description' => '<p>Despite the essentiality for faithful chromosome segregation, centromere architectures are diverse among eukaryotes and embody two main configurations: mono- and holocentromeres, referring, respectively, to localized or unrestricted distribution of centromeric activity. Of the two, some holocentromeres offer the curious condition of having arisen independently in multiple insects, most of which have lost the otherwise essential centromere-specifying factor CenH3 (first described as CENP-A in humans). The loss of CenH3 raises intuitive questions about how holocentromeres are organized and regulated in CenH3-lacking insects. Here, we report the first chromatin-level description of CenH3-deficient holocentromeres by leveraging recently identified centromere components and genomics approaches to map and characterize the holocentromeres of the silk moth Bombyx mori, a representative lepidopteran insect lacking CenH3. This uncovered a robust correlation between the distribution of centromere sites and regions of low chromatin activity along B. mori chromosomes. Transcriptional perturbation experiments recapitulated the exclusion of B. mori centromeres from active chromatin. Based on reciprocal centromere occupancy patterns observed along differentially expressed orthologous genes of Lepidoptera, we further found that holocentromere formation in a manner that is recessive to chromatin dynamics is evolutionarily conserved. Our results help us discuss the plasticity of centromeres in the context of a role for the chromosome-wide chromatin landscape in conferring centromere identity rather than the presence of CenH3. Given the co-occurrence of CenH3 loss and holocentricity in insects, we further propose that the evolutionary establishment of holocentromeres in insects was facilitated through the loss of a CenH3-specified centromere.</p>', 'date' => '2020-10-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/33125865', 'doi' => '10.1016/j.cub.2020.09.078', 'modified' => '2021-03-17 17:13:50', 'created' => '2021-02-18 10:21:53', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 2 => array( 'id' => '3598', 'name' => 'Novel dual regulators of Pseudomonas aeruginosa essential for productive biofilms and virulence.', 'authors' => 'Heacock-Kang Y, Zarzycki-Siek J, Sun Z, Poonsuk K, Bluhm AP, Cabanas D, Fogen D, McMillan IA, Chuanchuen R, Hoang TT', 'description' => '<p>Gene regulation network in Pseudomonas aeruginosa is complex. With a relatively large genome (6.2 Mb), there is a significant portion of genes that are proven or predicted to be transcriptional regulators. Many of these regulators have been shown to play important roles in biofilm formation and maintenance. In this study, we present a novel transcriptional regulator, PA1226, which modulates biofilm formation and virulence in P. aeruginosa. Mutation in the gene encoding this regulator abolished the ability of P. aeruginosa to produce biofilms in vitro, without any effect on the planktonic growth. This regulator is also essential for the in vivo fitness and pathogenesis in both Drosophila melanogaster and BALB/c mouse lung infection models. Transcriptome analysis revealed that PA1226 regulates many essential virulence genes/pathways, including those involved in alginate, pili, and LPS biosynthesis. Genes/operons directly regulated by PA1226 and potential binding sequences were identified via ChIP-seq. Attempts to confirm the binding sequences by electrophoretic mobility shift assay led to the discovery of a co-regulator, PA1413, via co-immunoprecipitation assay. PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. 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', 'description' => '<p>Burkholderia pseudomallei (Bp) is the causative agent of melioidosis, a disease endemic to the tropics. Melioidosis manifests in various ways ranging from acute skin lesions to pneumonia and, in rare cases, infection of the central nervous system. Bp is a facultative intracellular pathogen and it can infect various cell types. The Bp intracellular lifecycle has been partially elucidated and is highly complex. Herein, we have identified a transcriptional regulator, BP1026B_II1198, that is differentially expressed as Bp transits through host cells. A deletion mutant of BP1026B_II1198 was attenuated in RAW264.7 cell and BALB/c mouse infection. To further characterize the function of this transcriptional regulator, we endeavored to determine the regulon of BP1026B_II1198. RNA-seq analysis showed the global picture of genes regulated while ChIP-seq analysis identified two specific BP1026B_II1198 binding regions on chromosome II. We investigated the transposon mutants of these genes controlled by BP1026B_II1198 and confirmed that these genes contribute to pathogenesis in RAW264.7 murine macrophage cells. Taken together, the data presented here shed light on the regulon of BP1026B_II1198 and its role during intracellular infection and highlights an integral portion of the highly complex regulation network of Bp during host infection.</p>', 'date' => '2021-05-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/34001967', 'doi' => '10.1038/s41598-021-89852-7', 'modified' => '2022-08-02 16:55:52', 'created' => '2022-05-19 10:41:50', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 1 => array( 'id' => '4092', 'name' => 'Formation of the CenH3-Deficient Holocentromere in Lepidoptera AvoidsActive Chromatin.', 'authors' => 'Senaratne, Aruni P and Muller, Héloïse and Fryer, Kelsey A and Kawamoto,Munetaka and Katsuma, Susumu and Drinnenberg, Ines A', 'description' => '<p>Despite the essentiality for faithful chromosome segregation, centromere architectures are diverse among eukaryotes and embody two main configurations: mono- and holocentromeres, referring, respectively, to localized or unrestricted distribution of centromeric activity. 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Based on reciprocal centromere occupancy patterns observed along differentially expressed orthologous genes of Lepidoptera, we further found that holocentromere formation in a manner that is recessive to chromatin dynamics is evolutionarily conserved. Our results help us discuss the plasticity of centromeres in the context of a role for the chromosome-wide chromatin landscape in conferring centromere identity rather than the presence of CenH3. Given the co-occurrence of CenH3 loss and holocentricity in insects, we further propose that the evolutionary establishment of holocentromeres in insects was facilitated through the loss of a CenH3-specified centromere.</p>', 'date' => '2020-10-01', 'pmid' => 'https://www.ncbi.nlm.nih.gov/pubmed/33125865', 'doi' => '10.1016/j.cub.2020.09.078', 'modified' => '2021-03-17 17:13:50', 'created' => '2021-02-18 10:21:53', 'ProductsPublication' => array( [maximum depth reached] ) ), (int) 2 => array( 'id' => '3598', 'name' => 'Novel dual regulators of Pseudomonas aeruginosa essential for productive biofilms and virulence.', 'authors' => 'Heacock-Kang Y, Zarzycki-Siek J, Sun Z, Poonsuk K, Bluhm AP, Cabanas D, Fogen D, McMillan IA, Chuanchuen R, Hoang TT', 'description' => '<p>Gene regulation network in Pseudomonas aeruginosa is complex. With a relatively large genome (6.2 Mb), there is a significant portion of genes that are proven or predicted to be transcriptional regulators. Many of these regulators have been shown to play important roles in biofilm formation and maintenance. In this study, we present a novel transcriptional regulator, PA1226, which modulates biofilm formation and virulence in P. aeruginosa. Mutation in the gene encoding this regulator abolished the ability of P. aeruginosa to produce biofilms in vitro, without any effect on the planktonic growth. This regulator is also essential for the in vivo fitness and pathogenesis in both Drosophila melanogaster and BALB/c mouse lung infection models. Transcriptome analysis revealed that PA1226 regulates many essential virulence genes/pathways, including those involved in alginate, pili, and LPS biosynthesis. Genes/operons directly regulated by PA1226 and potential binding sequences were identified via ChIP-seq. Attempts to confirm the binding sequences by electrophoretic mobility shift assay led to the discovery of a co-regulator, PA1413, via co-immunoprecipitation assay. PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. A model is proposed, summarizing our finding on this novel dual-regulation system.</p>', 'date' => '2018-08-01', 'pmid' => 'http://www.pubmed.gov/29995308', 'doi' => '10.1111/mmi.14063', 'modified' => '2019-04-17 15:07:51', 'created' => '2019-04-16 12:25:30', 'ProductsPublication' => array( [maximum depth reached] ) ) ), 'Testimonial' => array(), 'Area' => array(), 'SafetySheet' => array( (int) 0 => array( 'id' => '336', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS US en', 'language' => 'en', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-US-en-GHS_1_0.pdf', 'countries' => 'US', 'modified' => '2020-06-09 13:03:27', 'created' => '2020-06-09 13:03:27', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 1 => array( 'id' => '334', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS GB en', 'language' => 'en', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-GB-en-GHS_1_0.pdf', 'countries' => 'GB', 'modified' => '2020-06-09 13:01:35', 'created' => '2020-06-09 13:01:35', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 2 => array( 'id' => '329', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS BE fr', 'language' => 'fr', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-BE-fr-GHS_1_0.pdf', 'countries' => 'BE', 'modified' => '2020-06-09 12:58:49', 'created' => '2020-06-09 12:58:49', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 3 => array( 'id' => '333', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS FR fr', 'language' => 'fr', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-FR-fr-GHS_1_0.pdf', 'countries' => 'FR', 'modified' => '2020-06-09 13:00:53', 'created' => '2020-06-09 13:00:53', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 4 => array( 'id' => '332', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS ES es', 'language' => 'es', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-ES-es-GHS_1_0.pdf', 'countries' => 'ES', 'modified' => '2020-06-09 13:00:23', 'created' => '2020-06-09 13:00:23', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 5 => array( 'id' => '331', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS DE de', 'language' => 'de', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-DE-de-GHS_1_0.pdf', 'countries' => 'DE', 'modified' => '2020-06-09 12:59:50', 'created' => '2020-06-09 12:59:50', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 6 => array( 'id' => '335', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS JP ja', 'language' => 'ja', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-JP-ja-GHS_2_0.pdf', 'countries' => 'JP', 'modified' => '2020-06-09 13:02:44', 'created' => '2020-06-09 13:02:44', 'ProductsSafetySheet' => array( [maximum depth reached] ) ), (int) 7 => array( 'id' => '330', 'name' => 'DiaMag anti-mouse IgG coated magnetic beads SDS BE nl', 'language' => 'nl', 'url' => 'files/SDS/DiaMag_anti-mouse/SDS-C03010022-DiaMag_anti-mouse_IgG_coated_magnetic_beads-BE-nl-GHS_1_0.pdf', 'countries' => 'BE', 'modified' => '2020-06-09 12:59:19', 'created' => '2020-06-09 12:59:19', 'ProductsSafetySheet' => array( [maximum depth reached] ) ) ) ) $meta_canonical = 'https://www.diagenode.com/jp/p/diamag-anti-mouse-igg-coated-magnetic-beads-220-ul' $country = 'US' $countries_allowed = array( (int) 0 => 'CA', (int) 1 => 'US', (int) 2 => 'IE', (int) 3 => 'GB', (int) 4 => 'DK', (int) 5 => 'NO', (int) 6 => 'SE', (int) 7 => 'FI', (int) 8 => 'NL', (int) 9 => 'BE', (int) 10 => 'LU', (int) 11 => 'FR', (int) 12 => 'DE', (int) 13 => 'CH', (int) 14 => 'AT', (int) 15 => 'ES', (int) 16 => 'IT', (int) 17 => 'PT' ) $outsource = false $other_formats = array( (int) 0 => array( 'id' => '1911', 'antibody_id' => null, 'name' => 'DiaMag anti-mouse IgG coated magnetic beads', 'description' => '<p><span>These magnetic beads coated with anti-mouse IgG antibody have been extensively validated in chromatin immunoprecipitation assay (ChIP) and methylated DNA immunoprecipitation assays (MeDIP). 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With a relatively large genome (6.2 Mb), there is a significant portion of genes that are proven or predicted to be transcriptional regulators. Many of these regulators have been shown to play important roles in biofilm formation and maintenance. In this study, we present a novel transcriptional regulator, PA1226, which modulates biofilm formation and virulence in P. aeruginosa. Mutation in the gene encoding this regulator abolished the ability of P. aeruginosa to produce biofilms in vitro, without any effect on the planktonic growth. This regulator is also essential for the in vivo fitness and pathogenesis in both Drosophila melanogaster and BALB/c mouse lung infection models. Transcriptome analysis revealed that PA1226 regulates many essential virulence genes/pathways, including those involved in alginate, pili, and LPS biosynthesis. Genes/operons directly regulated by PA1226 and potential binding sequences were identified via ChIP-seq. Attempts to confirm the binding sequences by electrophoretic mobility shift assay led to the discovery of a co-regulator, PA1413, via co-immunoprecipitation assay. PA1226 and PA1413 were shown to bind collaboratively to the promoter regions of their regulons. A model is proposed, summarizing our finding on this novel dual-regulation system.</p>', 'date' => '2018-08-01', 'pmid' => 'http://www.pubmed.gov/29995308', 'doi' => '10.1111/mmi.14063', 'modified' => '2019-04-17 15:07:51', 'created' => '2019-04-16 12:25:30', 'ProductsPublication' => array( 'id' => '3469', 'product_id' => '1910', 'publication_id' => '3598' ) ) $externalLink = ' <a href="http://www.pubmed.gov/29995308" 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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