期刊
ANALYTICAL CHEMISTRY
卷 80, 期 9, 页码 3483-3491出版社
AMER CHEMICAL SOC
DOI: 10.1021/ac8002352
关键词
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资金
- NHGRI NIH HHS [R01-HG001499, R01 HG001499-09, R01 HG001499] Funding Source: Medline
We report a simple and effective method for the high-throughput purification of a variety of nucleic acids (NAs) from whole cell lysates or whole blood using a photactivated polycarbonate solid-phase reversible immobilization (PPC-SPRI) microfluidic chip. High-throughput operation was achieved by placing 96 purification beds, each containing an array of 3800 20 pm diameter posts, on a single 3 x 5 polycarbonate (PC) wafer fabricated by hot embossing. All beds were interconnected through a common microfluidic network that permitted parallel access through the use of a vacuum and syringe pump for delivery of immobilization buffer (IB) and effluent. The PPC-SPRI purification was accomplished by condensation of NAs onto a UV-modified PC surface in the presence of the IB comprised of polyethylene glycol, NaCl, and ethanol with a composition dependent on the length of the NAs to be isolated and the identity of the sample matrix. The performance of the device was validated by quantification of the recovered material following PCR (for DNA) or RTPCR (for RNA). The extraction bed load capacity of NAs was 206 +/- 93 ng for gDNA and 165 +/- 81 ng for TRNA from Escherichia coli. Plate-to-plate variability was found to be 35 +/- 10%. The purification process was fast (< 30 min) and easy to automate, and the low cost of wafer fabrication makes it appropriate for single-use applications.
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