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Application of a Multi-Channel Microfluidic Chip on the Simultaneous Detection of DNAs by Using Microbead-Quantum Dots

机译:多通道微流控芯片在微珠-量子点同时检测DNA中的应用

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Several researches have shown that cancer is caused by genetic mutations especially in genes involved in cell growth and regulation. Ras family members are frequently found in their mutated, oncogenic forms in human tumors. Mutant RAS proteins are constitutively active, owing to reduce intrinsic GTPase activity and insensitivity to GTPase-activating protein (GAPs). In total, activating mutations in the RAS genes occur in approximately 20% of all human cancers, mainly in codon 12, 13 or 61. Activating mutations in the NRAS gene not only result in the reduction of intrinsic GTPase activity but also in the induction of resistance against molecules inducing such activity. In this paper, we reported a rapid, simple and portable method for detecting the mutant types of NRAS genes codon 12 and 61 simultaneously by using bead-quantum dots (QDs) based multi-channel microfluidic chip. Probe DNAs are conjugated to bead-QDs and packed in the pillars of channels in the microfluidic chip. After injection of target DNAs and intercalating dyes, the fluorescence quenching of QDs by intercalating dye was observed due to FRET phenomena. The platform can be effortlessly applied in other biological and clinical areas.
机译:多项研究表明,癌症是由基因突变引起的,尤其是与细胞生长和调控有关的基因。 Ras家族成员经常以突变,致癌形式在人类肿瘤中发现。突变的RAS蛋白具有组成型活性,因为它降低了固有的GTPase活性和对GTPase激活蛋白(GAPs)的敏感性。总体而言,RAS基因中的激活突变发生在大约20%的所有人类癌症中,主要发生在密码子12、13或61中。NRAS基因中的激活突变不仅导致内在GTPase活性降低,而且还导致了GTPase的诱导。对诱导此类活性的分子具有抗性。在本文中,我们报告了一种快速,简单且可移植的方法,该方法可通过使用基于珠量子点(QD)的多通道微流控芯片同时检测NRAS基因密码子12和61的突变类型。探针DNA与珠QD结合,并堆积在微流控芯片通道的柱子中。注入目标DNA和嵌入染料后,由于FRET现象,观察到了嵌入染料对量子点的荧光猝灭。该平台可轻松应用于其他生物学和临床领域。

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