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Pinched flow fractionation devices for detection of single nucleotide polymorphisms

机译:用于单核苷酸多态性检测的夹流分离装置

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摘要

We demonstrate a new and flexible micro fluidic based method for genotyping single nucleotide polymorphisms ( SNPs). The method relies on size separation of selectively hybridized polystyrene microspheres in a micro fluidic pinched flow fractionation (PFF) device. The micro fluidic PFF devices with 13 mu m deep channels were fabricated by thermal nanoimprint lithography ( NIL) in a thin film of cyclic-olefin copolymer (mr-I T85) on a silicon wafer substrate, and the channels were sealed by thermal polymer bonding. Streptavidin coated polystyrene microspheres with a mean diameter of 3.09 mu m and 5.6 mu m were functionalized with biotin-labeled oligonucleotides for the detection of a mutant (Mt) or wild-type (Wt) DNA sequence in the HBB gene, respectively. Hybridization to functionalized beads was performed with fluorescent targets comprising synthetic DNA oligonucleotides or amplified RNA, synthesized using human DNA samples from individuals with point mutations in the HBB gene. Following a stringent wash, the beads were separated in a PFF device and the fluorescent signal from the beads was analyzed. Patients being wildtypes, heterozygotes or mutated respectively for the investigated mutation could reliably be diagnosed in the PFF device. This indicates that the PFF technique can be used for accurate and fast genotyping of SNPs.
机译:我们演示了一种新的和灵活的基于微流体的基因型单核苷酸多态性(SNPs)的方法。该方法依赖于微流体夹流分馏(PFF)设备中选择性杂交的聚苯乙烯微球的尺寸分离。通过热纳米压印光刻(NIL)在硅晶片基板上的环状烯烃共聚物(mr-I T85)薄膜中制造了具有13微米深通道的微流体PFF器件,并通过热聚合物键合密封通道。用生物素标记的寡核苷酸对平均直径为3.09μm和5.6μm的链霉亲和素包被的聚苯乙烯微球进行功能化,以分别检测HBB基因中的突变(Mt)或野生型(Wt)DNA序列。使用包含合成DNA寡核苷酸或扩增的RNA的荧光靶标与功能化的珠子杂交,该荧光标靶使用来自HBB基因中具有点突变的个体的人DNA样品合成。严格洗涤后,在PFF装置中分离珠子,并分析来自珠子的荧光信号。可以分别在PFF装置中可靠地诊断出是野生型,杂合子或突变的患者。这表明PFF技术可用于SNP的准确快速基因分型。

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