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96
New England Biolabs vaccinia ce vce
( A ) Diagram of the in vivo capping activity assay. The construction details of the K1.5/T7 transcriptional system used for the in vivo assays are shown in fig. S15. YFP, yellow fluorescent protein. ( B ) The capping activities of 46 text-mined CEs in CHO cells. The RNAP not fused to a CE served as the negative control (NO_CE, blue bar), and the RNAP fused to the NP868R CE served as the positive control (gray bar and blue dashed line). The relative activities were calculated by assigning the NO_CE mean fluorescence intensity as 1. The bar plot shows the means ± SD of three biological replicates. Sequences chosen for yeast evaluation are marked by orange dots. Data are found in table S5. ( C ) The capping activities of 18 text-mined CEs in S. cerevisiae . Controls, error bars, and color coding are the same as in (B). ( D ) Diagram of the in vitro capping activity assay. ( E ) The in vitro capping activities of two <t>CEs</t> <t>(MRV_5</t> and MRV_6) found in this work compared with commercial vaccinia CE <t>(VCE)</t> (control_NEB) and no enzyme treatment control (control_NoEnzyme). Each group includes three biological replicates, with representative mass spectra shown. The x axis represents the molecular weight of the compounds, with the observed mass displayed above the corresponding peaks (amu, the relative atomic mass unit). The y axis is the count of compounds collected. For compound identities and liquid chromatography–mass spectrometry (LC-MS) results of all experiments, see figs. S22 to S25 and table S6. The bar plot shows the means ± SD of three biological replicates. P values were determined using an unpaired two-sided t test.
Vaccinia Ce Vce, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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96
New England Biolabs vce
( A ) Diagram of the in vivo capping activity assay. The construction details of the K1.5/T7 transcriptional system used for the in vivo assays are shown in fig. S15. YFP, yellow fluorescent protein. ( B ) The capping activities of 46 text-mined CEs in CHO cells. The RNAP not fused to a CE served as the negative control (NO_CE, blue bar), and the RNAP fused to the NP868R CE served as the positive control (gray bar and blue dashed line). The relative activities were calculated by assigning the NO_CE mean fluorescence intensity as 1. The bar plot shows the means ± SD of three biological replicates. Sequences chosen for yeast evaluation are marked by orange dots. Data are found in table S5. ( C ) The capping activities of 18 text-mined CEs in S. cerevisiae . Controls, error bars, and color coding are the same as in (B). ( D ) Diagram of the in vitro capping activity assay. ( E ) The in vitro capping activities of two <t>CEs</t> <t>(MRV_5</t> and MRV_6) found in this work compared with commercial vaccinia CE <t>(VCE)</t> (control_NEB) and no enzyme treatment control (control_NoEnzyme). Each group includes three biological replicates, with representative mass spectra shown. The x axis represents the molecular weight of the compounds, with the observed mass displayed above the corresponding peaks (amu, the relative atomic mass unit). The y axis is the count of compounds collected. For compound identities and liquid chromatography–mass spectrometry (LC-MS) results of all experiments, see figs. S22 to S25 and table S6. The bar plot shows the means ± SD of three biological replicates. P values were determined using an unpaired two-sided t test.
Vce, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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90
IntroMedic Co Ltd rt-vce system mirocam mc1200
( A ) Diagram of the in vivo capping activity assay. The construction details of the K1.5/T7 transcriptional system used for the in vivo assays are shown in fig. S15. YFP, yellow fluorescent protein. ( B ) The capping activities of 46 text-mined CEs in CHO cells. The RNAP not fused to a CE served as the negative control (NO_CE, blue bar), and the RNAP fused to the NP868R CE served as the positive control (gray bar and blue dashed line). The relative activities were calculated by assigning the NO_CE mean fluorescence intensity as 1. The bar plot shows the means ± SD of three biological replicates. Sequences chosen for yeast evaluation are marked by orange dots. Data are found in table S5. ( C ) The capping activities of 18 text-mined CEs in S. cerevisiae . Controls, error bars, and color coding are the same as in (B). ( D ) Diagram of the in vitro capping activity assay. ( E ) The in vitro capping activities of two <t>CEs</t> <t>(MRV_5</t> and MRV_6) found in this work compared with commercial vaccinia CE <t>(VCE)</t> (control_NEB) and no enzyme treatment control (control_NoEnzyme). Each group includes three biological replicates, with representative mass spectra shown. The x axis represents the molecular weight of the compounds, with the observed mass displayed above the corresponding peaks (amu, the relative atomic mass unit). The y axis is the count of compounds collected. For compound identities and liquid chromatography–mass spectrometry (LC-MS) results of all experiments, see figs. S22 to S25 and table S6. The bar plot shows the means ± SD of three biological replicates. P values were determined using an unpaired two-sided t test.
Rt Vce System Mirocam Mc1200, supplied by IntroMedic Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rt-vce system mirocam mc1200/product/IntroMedic Co Ltd
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IntroMedic Co Ltd vce devices from intromedic mirocam system
Characteristics of pediatric patients with Crohn's disease undergoing <t> VCE </t> between years 2003 and 2023.
Vce Devices From Intromedic Mirocam System, supplied by IntroMedic Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
vce devices from intromedic mirocam system - by Bioz Stars, 2026-06
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( A ) Diagram of the in vivo capping activity assay. The construction details of the K1.5/T7 transcriptional system used for the in vivo assays are shown in fig. S15. YFP, yellow fluorescent protein. ( B ) The capping activities of 46 text-mined CEs in CHO cells. The RNAP not fused to a CE served as the negative control (NO_CE, blue bar), and the RNAP fused to the NP868R CE served as the positive control (gray bar and blue dashed line). The relative activities were calculated by assigning the NO_CE mean fluorescence intensity as 1. The bar plot shows the means ± SD of three biological replicates. Sequences chosen for yeast evaluation are marked by orange dots. Data are found in table S5. ( C ) The capping activities of 18 text-mined CEs in S. cerevisiae . Controls, error bars, and color coding are the same as in (B). ( D ) Diagram of the in vitro capping activity assay. ( E ) The in vitro capping activities of two CEs (MRV_5 and MRV_6) found in this work compared with commercial vaccinia CE (VCE) (control_NEB) and no enzyme treatment control (control_NoEnzyme). Each group includes three biological replicates, with representative mass spectra shown. The x axis represents the molecular weight of the compounds, with the observed mass displayed above the corresponding peaks (amu, the relative atomic mass unit). The y axis is the count of compounds collected. For compound identities and liquid chromatography–mass spectrometry (LC-MS) results of all experiments, see figs. S22 to S25 and table S6. The bar plot shows the means ± SD of three biological replicates. P values were determined using an unpaired two-sided t test.

Journal: Science Advances

Article Title: Discovery of diverse and high-quality mRNA capping enzymes through a language model–enabled platform

doi: 10.1126/sciadv.adt0402

Figure Lengend Snippet: ( A ) Diagram of the in vivo capping activity assay. The construction details of the K1.5/T7 transcriptional system used for the in vivo assays are shown in fig. S15. YFP, yellow fluorescent protein. ( B ) The capping activities of 46 text-mined CEs in CHO cells. The RNAP not fused to a CE served as the negative control (NO_CE, blue bar), and the RNAP fused to the NP868R CE served as the positive control (gray bar and blue dashed line). The relative activities were calculated by assigning the NO_CE mean fluorescence intensity as 1. The bar plot shows the means ± SD of three biological replicates. Sequences chosen for yeast evaluation are marked by orange dots. Data are found in table S5. ( C ) The capping activities of 18 text-mined CEs in S. cerevisiae . Controls, error bars, and color coding are the same as in (B). ( D ) Diagram of the in vitro capping activity assay. ( E ) The in vitro capping activities of two CEs (MRV_5 and MRV_6) found in this work compared with commercial vaccinia CE (VCE) (control_NEB) and no enzyme treatment control (control_NoEnzyme). Each group includes three biological replicates, with representative mass spectra shown. The x axis represents the molecular weight of the compounds, with the observed mass displayed above the corresponding peaks (amu, the relative atomic mass unit). The y axis is the count of compounds collected. For compound identities and liquid chromatography–mass spectrometry (LC-MS) results of all experiments, see figs. S22 to S25 and table S6. The bar plot shows the means ± SD of three biological replicates. P values were determined using an unpaired two-sided t test.

Article Snippet: With the same enzyme usage and reaction conditions, both MRV_5 and MRV_6 [Marseilleviridae CEs (MCEs)] exhibited twofold enhanced capping efficiencies to the commercial vaccinia CE (VCE) from New England Biolabs (NEB; and figs. S22 to S25).

Techniques: In Vivo, Activity Assay, Negative Control, Positive Control, Fluorescence, In Vitro, Control, Molecular Weight, Liquid Chromatography, Mass Spectrometry, Liquid Chromatography with Mass Spectroscopy

Characteristics of pediatric patients with Crohn's disease undergoing  VCE  between years 2003 and 2023.

Journal: Journal of Pediatric Gastroenterology and Nutrition

Article Title: Long‐term follow‐up of children with Crohn's disease and small bowel mucosal lesions detected through video capsule endoscopy

doi: 10.1002/jpn3.12397

Figure Lengend Snippet: Characteristics of pediatric patients with Crohn's disease undergoing VCE between years 2003 and 2023.

Article Snippet: VCEs were performed at the clinician's discretion using clinically available standard VCE devices from Given Pillcam system (years 2003–2019) or IntroMedic Mirocam system (years 2012–2023).

Techniques: Biomarker Discovery, Medications