Lee Se Hee, Lee Ho Won, Kim Da Som, Kwon Hyuck Gi, Lee Jong Hyun, Kim Yang-Hoon, Jeong Ok Chan, Ahn Ji-Young
College of Natural Sciences, Chungbuk National University.
Department of Biomedical Engineering, Inje University.
J Vis Exp. 2018 Nov 14(141). doi: 10.3791/57703.
Droplet-based microfluidics enable the reliable production of homogeneous microspheres in the microfluidic channel, providing controlled size and morphology of the obtained microsphere. A microsphere copolymerized with an acrydite-DNA probe was successfully fabricated. Different methods such as asymmetric PCR, exonuclease digestion, and isolation on streptavidin-coated magnetic beads can be used to synthesize single-stranded DNA (ssDNA). However, these methods cannot efficiently use large amounts of highly purified ssDNA. Here, we describe a microsphere-PCR protocol detailing how ssDNA can be efficiently amplified and separated from dsDNA simply by pipetting from a PCR reaction tube. The amplification of ssDNA can be applied as potential reagents for the DNA microarray and DNA-SELEX (Systematic evolution of ligands by exponential enrichment) processes.
基于液滴的微流控技术能够在微流控通道中可靠地生产均匀的微球,从而控制所得微球的大小和形态。成功制备了与丙烯酰胺-DNA探针共聚的微球。诸如不对称PCR、核酸外切酶消化以及在链霉亲和素包被的磁珠上进行分离等不同方法可用于合成单链DNA(ssDNA)。然而,这些方法无法高效利用大量高度纯化的ssDNA。在此,我们描述了一种微球-PCR方案,详细说明了如何仅通过从PCR反应管中移液就能有效地扩增ssDNA并将其与双链DNA(dsDNA)分离。ssDNA的扩增可作为DNA微阵列和DNA-SELEX(指数富集配体系统进化)过程的潜在试剂。