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Production by quantitative photolithographic synthesis of individually quality checked DNA microarrays

机译:通过定量光刻合成单独质量检查的DNA微阵列进行生产

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摘要

For DNA chip analyses, oligonucleotide quality has immense consequences for accuracy, sensitivity and dynamic range. The quality of chips produced by photolithographic in situ synthesis depends critically on the efficiency of photo-deprotection. By means of base-assisted enhancement of this process using 5′-[2-(2-nitrophenyl)-propyloxycarbonyl]-2′-deoxynucleoside phosphoramidites, synthesis yields improved by at least 12% per condensation compared to current chemistries. Thus, the eventual total yield of full-length oligonucleotide is increased more than 10-fold in the case of 20mers. Furthermore, the quality of every individual array position was checked quantitatively after synthesis. Subsequently, the quality tested chips were used in successive hybridisation experiments.
机译:对于DNA芯片分析,寡核苷酸质量对准确性,灵敏度和动态范围具有巨大影响。通过光刻原位合成生产的芯片的质量关键取决于光脱保护的效率。通过使用5'-[2-(2-硝基苯基)-丙氧基羰基] -2'-脱氧核苷亚磷酰胺的碱辅助增强方法,与目前的化学方法相比,每次缩合反应的合成产率提高了至少12%。因此,在20聚体的情况下,全长寡核苷酸的最终总产量增加了10倍以上。此外,合成后定量检查每个单独阵列位置的质量。随后,将经过质量测试的芯片用于后续的杂交实验。

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