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Probe-on-carriers for oligonucleotide microarrays (DNA chips)

机译:寡核苷酸微阵列(DNA芯片)的载体探针

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摘要

Oigonucleotide microarrays (DNA chips) are very efficient tools to analyze genotypes of patients or change in gene expressions between two different samples. However, there is no cost effective procedure to manufacture DNA chips. We are developing 'probe-on-carriers', immobilized oligonucleotide probes on solid phase to make DNA chips. In this procedure, each oligonucleotide is synthesized on a controlled porous glass carrier as a solid phase, and can be used as a probe for each sequence. This can be substantiated by technology for strictly controlled pore-size of porous glass. In fact, we found the sequence specific hybridization of probe-on-carrier with using porous glass of larger than 50 nm pore diameter. The probe-on-carriers for wildtype and mutant p53 genes were hybridized with their complementary probes, respectively, but not with another probes. This result clearly demonstrated that the probe-on-carriers could recognize one-nucleotide substitutions of a gene. We found that the fixed probe-on-carriers on a slide glass still showed sequence specific hybridization. Therefore, we conclude that the probe-on-carriers are epoch-making materials for making DNA chip economically.
机译:寡核苷酸微阵列(DNA芯片)是分析患者基因型或两个不同样本之间基因表达变化的非常有效的工具。但是,没有成本有效的程序来制造DNA芯片。我们正在开发“载体探针”,将固相寡核苷酸探针固定在固相上以制备DNA芯片。在该程序中,每种寡核苷酸都在固相多孔多孔玻璃载体上合成,并可用作每种序列的探针。严格控制多孔玻璃孔径的技术可以证明这一点。实际上,我们发现了使用孔径大于50 nm的多孔玻璃对探针进行序列特异性杂交。将野生型和突变型p53基因的载体探针分别与它们的互补探针杂交,但不与其他探针杂交。该结果清楚地表明,载体探针可以识别基因的一个核苷酸取代。我们发现载玻片上固定的探针在载体上仍然显示出序列特异性杂交。因此,我们得出的结论是,探针载体是划时代的材料,可以经济地制造DNA芯片。

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