艾默生网络能源旗下的Lieberte XM系列中功率UPS,在前不久落幕的＂2016年度中国优秀数据中心评选＂中斩获＂示范产品奖＂殊荣,再次彰显了艾默生网络能源在UPS领域强大的品牌实力以及产品的一流品质。创新产品提升客户价值Liebert e XM...艾默生网络能源旗下的Lieberte XM系列中功率UPS,在前不久落幕的＂2016年度中国优秀数据中心评选＂中斩获＂示范产品奖＂殊荣,再次彰显了艾默生网络能源在UPS领域强大的品牌实力以及产品的一流品质。创新产品提升客户价值Liebert e XM系列中功率UPS是一款专门适用于中小规模机房的创新产品,展开更多
Imaging-based phenotypic screening uses cellular phenotypes to describe the drug performance, which generally focuses on single cellular feature, lacking of a comprehensive characterization. Here, we propose a high co...Imaging-based phenotypic screening uses cellular phenotypes to describe the drug performance, which generally focuses on single cellular feature, lacking of a comprehensive characterization. Here, we propose a high content phenotypic screening method based on expansion microscopy(ExM) assisted cell painting, which enables multi-channel imaging with approximately 50 nm resolution. As a demonstration, we applied this method to a phenotypic screening involving five drugs. The morphological attributes of three subcellular structures were summarized to consist a “fingerprint” describing the drug effect. The proposed method can provide comprehensive and detailed clues for drug evaluation, enriching the content of phenotypic screening.展开更多
文摘艾默生网络能源旗下的Lieberte XM系列中功率UPS,在前不久落幕的＂2016年度中国优秀数据中心评选＂中斩获＂示范产品奖＂殊荣,再次彰显了艾默生网络能源在UPS领域强大的品牌实力以及产品的一流品质。创新产品提升客户价值Liebert e XM系列中功率UPS是一款专门适用于中小规模机房的创新产品,
基金supported by the National Key R&D Program of China(No.2022YFC2409603)the Tianjin Municipal Science and Technology Program(No.23JCZXJC00340)the Beijing-Tianjin-Hebei Fundamental Research Cooperation Project(No.J230001)。
文摘Imaging-based phenotypic screening uses cellular phenotypes to describe the drug performance, which generally focuses on single cellular feature, lacking of a comprehensive characterization. Here, we propose a high content phenotypic screening method based on expansion microscopy(ExM) assisted cell painting, which enables multi-channel imaging with approximately 50 nm resolution. As a demonstration, we applied this method to a phenotypic screening involving five drugs. The morphological attributes of three subcellular structures were summarized to consist a “fingerprint” describing the drug effect. The proposed method can provide comprehensive and detailed clues for drug evaluation, enriching the content of phenotypic screening.
