A nanoliter-scale nucleic acid processor with parallel architecture

被引:354
作者
Hong, JW
Studer, V
Hang, G
Anderson, WF
Quake, SR [1 ]
机构
[1] CALTECH, Dept Appl Phys, Pasadena, CA 91125 USA
[2] CNRS, LPN Lab Photon & Nanostruct, F-91460 Marcoussis, France
[3] Univ So Calif, Keck Sch Med, Gene Therapy Labs, Los Angeles, CA 90033 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nbt951
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The purification of nucleic acids from microbial and mammalian cells is a crucial step in many biological and medical applications(1). We have developed microfluidic chips for automated nucleic acid purification from small numbers of bacterial or mammalian cells. All processes, such as cell isolation, cell lysis, DNA or mRNA purification, and recovery, were carried out on a single microfluidic chip in nanoliter volumes without any pre- or postsample treatment. Measurable amounts of mRNA were extracted in an automated fashion from as little as a single mammalian cell and recovered from the chip. These microfluidic chips are capable of processing different samples in parallel, thereby illustrating how highly parallel microfluidic architectures can be constructed to perform integrated batch-processing functionalities for biological and medical applications.
引用
收藏
页码:435 / 439
页数:5
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