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制造具有高斑点均匀性和降低背景信号的DNA微阵列。

Manufacturing DNA microarrays of high spot homogeneity and reduced background signal.

作者信息

Diehl F, Grahlmann S, Beier M, Hoheisel J D

机构信息

Functional Genome Analysis, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 506, D-69120 Heidelberg, Germany.

出版信息

Nucleic Acids Res. 2001 Apr 1;29(7):E38. doi: 10.1093/nar/29.7.e38.

Abstract

Analyses on DNA microarrays depend considerably on spot quality and a low background signal of the glass support. By using betaine as an additive to a spotting solution made of saline sodium citrate, both the binding efficiency of spotted PCR products and the homogeneity of the DNA spots is improved significantly on aminated surfaces such as glass slides coated with the widely used poly-L-lysine or aminosilane. In addition, non-specific background signal is markedly diminished. Concomitantly, during the arraying procedure, the betaine reduces evaporation from the microtitre dish wells, which hold the PCR products. Subsequent blocking of the chip surface with succinic anhydride was improved considerably in the presence of the non-polar, non-aqueous solvent 1,2-dichloroethane and the acylating catalyst N:-methylimidazole. This procedure prevents the overall background signal that occurs with the frequently applied aqueous solvent 1-methyl-2-pyrrolidone in borate buffer because of DNA that re-dissolves from spots during the blocking process, only to bind again across the entire glass surface.

摘要

DNA微阵列分析在很大程度上取决于斑点质量和玻璃载体的低背景信号。通过将甜菜碱作为添加剂添加到由柠檬酸钠盐水制成的点样溶液中,在诸如涂有广泛使用的聚-L-赖氨酸或氨基硅烷的载玻片等胺化表面上,点样的PCR产物的结合效率和DNA斑点的均匀性均得到显著提高。此外,非特异性背景信号明显减弱。同时,在点样过程中,甜菜碱减少了容纳PCR产物的微量滴定板孔中的蒸发。在非极性非水溶剂1,2-二氯乙烷和酰化催化剂N-甲基咪唑存在的情况下,用琥珀酸酐对芯片表面进行的后续封闭有了很大改进。该程序可防止由于在封闭过程中从斑点中重新溶解的DNA而在硼酸盐缓冲液中频繁使用的水性溶剂1-甲基-2-吡咯烷酮所产生的整体背景信号,这些DNA只会再次结合在整个玻璃表面上。

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本文引用的文献

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