Radioactive 33-P probes in hybridization to glass cDNA microarrays using neural tissues

被引:11
作者
Whitney, LW
Becker, KG
机构
[1] NIA, DNA Array Unit, NIH, Gerontol Res Ctr, Baltimore, MD 21224 USA
[2] NINDS, Mol Immunol Sect, Neuroimmunol Branch, NIH, Bethesda, MD 20892 USA
关键词
cDNA microarray; brain; hybridization; radioactive; probe;
D O I
10.1016/S0165-0270(00)00370-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
cDNA microarrays are becoming widespread tools in the study of complex gene expression patterns with applications using cells lines, animal model systems, and human disease. Class cDNA microarrays using fluorescent labeled cDNA probes require a large amount of input RNA usually not available in man): neuroscience applications. Here we demonstrate a technique for the use of 33-P labeled cDNA probes in hybridizations to the same glass cDNA arrays used for fluorescent applications. This approach allows the use of low quantities of RNA, common phosphoimaging scanners, data acquisition software, and standard DNA and RNA labeling protocols, while being consistent and interchangeable with glass-based cDNA array technology. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:9 / 13
页数:5
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