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Robust and efficient synthetic method for forming DNA microarrays

机译:形成DNA微阵列的稳健而有效的合成方法

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The field of DNA microarray technology has necessitated the cooperative efforts of interdisciplinary scientific teams to achieve its primary goal of rapidly measuring global gene expression patterns. A collaborative effort was established to produce a chemically reactive surface on glass slide substrates to which unmodified DNA will covalently bind for improvement of cDNA microarray technology. Using the p-aminophenyl trimethoxysilane (ATMS)/diazotization chemistry that was developed, microarrays were fabricated and analyzed. This immobilization method produced uniform spots containing equivalent or greater amounts of DNA than commercially available immobilization techniques. In addition, hybridization analyses of microarrays made with ATMS/diazotization chemistry showed very sensitive detection of the target sequence, two to three orders of magnitude more sensitive than the commercial chemistries. Repeated stripping and re-hybridization of these slides showed that DNA loss was minimal, allowing multiple rounds of hybridization. Thus, the ATMS/diazotization chemistry facilitated covalent binding of unmodified DNA, and the reusable microarrays that were produced showed enhanced levels of hybridization and very low background fluorescence.
机译:DNA微阵列技术领域已需要跨学科的科研团队共同努力,以实现其快速测量全球基因表达模式的主要目标。建立了合作关系以在载玻片基材上产生化学反应性表面,未修饰的DNA将与之共价结合以改善cDNA微阵列技术。使用已开发的对氨基苯基三甲氧基硅烷(ATMS)/重氮化化学方法,制造并分析了微阵列。这种固定方法产生的均匀斑点比市售固定技术含有相等或更多量的DNA。此外,用ATMS /重氮化化学方法对微阵列进行的杂交分析表明,对靶序列的检测非常灵敏,其灵敏度比市售化学试剂高2至3个数量级。重复剥离和重新杂交这些载玻片表明,DNA的损失很小,可以进行多轮杂交。因此,ATMS /重氮化化学促进了未修饰DNA的共价结合,并且产生的可重复使用的微阵列显示出增强的杂交水平和非常低的背景荧光。

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