多路复用
微流控
分析物
生物分子
纳米技术
吞吐量
计算机科学
计算生物学
化学
材料科学
生物
色谱法
电信
无线
作者
Daniel C. Pregibon,Mehmet Toner,Patrick S. Doyle
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2007-03-08
卷期号:315 (5817): 1393-1396
被引量:728
标识
DOI:10.1126/science.1134929
摘要
High-throughput screening for genetic analysis, combinatorial chemistry, and clinical diagnostics benefits from multiplexing, which allows for the simultaneous assay of several analytes but necessitates an encoding scheme for molecular identification. Current approaches for multiplexed analysis involve complicated or expensive processes for encoding, functionalizing, or decoding active substrates (particles or surfaces) and often yield a very limited number of analyte-specific codes. We present a method based on continuous-flow lithography that combines particle synthesis and encoding and probe incorporation into a single process to generate multifunctional particles bearing over a million unique codes. By using such particles, we demonstrate a multiplexed, single-fluorescence detection of DNA oligomers with encoded particle libraries that can be scanned rapidly in a flow-through microfluidic channel. Furthermore, we demonstrate with high specificity the same multiplexed detection using individual multiprobe particles.
科研通智能强力驱动
Strongly Powered by AbleSci AI