首页> 外文会议>Conference on Biomedical Nanotechnology Architectures and Applications Jan 20-24, 2002 San Jose, USA >Miniaturization of Ultra-High-Throughput Screening Assays into 1536-well Format
【24h】

Miniaturization of Ultra-High-Throughput Screening Assays into 1536-well Format

机译:超高通量筛选方法的小型化为1536孔形式

获取原文
获取原文并翻译 | 示例

摘要

Assay miniaturization and the implementation of high-density 1536 micro-well screening increases the speed and efficiency of screening and lead discovery. To serve this need, a platform of miniaturizable assay technologies has been assembled for specific biological targets. This platform will enable initiation and completion of uHTS screens in a straightforward and expeditious manner. For kinases, we have examined assays using several technologies including DELFIA, HTR-FRET, FP, EFC, and FMAT. This presentation compares these technologies for the measurement of typical tyrosine kinase activity in 1536-well format. Quality parameters such as assay reproducibility, signal:background ratio, Z factor, and assay sensitivity were calculated and compared. Additionally, the relative merits of each of these technologies were assessed in terms of assay miniaturization, ease of development, ultimate screening capability, efficiency, and cost.
机译:分析的小型化和高密度1536微孔筛查的实施提高了筛查和潜在顾客发现的速度和效率。为了满足这一需求,已经针对特定的生物靶标组装了小型化测定技术的平台。该平台将使直接,快速地启动和完成uHTS屏幕成为可能。对于激酶,我们已经使用包括DELFIA,HTR-FRET,FP,EFC和FMAT在内的多种技术检查了检测方法。本演示文稿比较了这些技术以1536孔形式测量典型酪氨酸激酶活性的方法。计算并比较了诸如测定重现性,信号:背景比,Z因子和测定灵敏度等质量参数。此外,根据测定的小型化,易于开发,最终筛选能力,效率和成本,评估了每种技术的相对优点。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号