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A common reference for cDNA microarray hybridizations - art. no. e116

机译:cDNA微阵列杂交的通用参考文献-art。没有。 e116

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Comparisons of expression levels across different cDNA microarray experiments are easier when a common reference is co-hybridized to every microarray. Often this reference consists of one experimental control sample, a pool of cell lines or a mix of all samples to be analyzed. We have developed an alternative common reference consisting of a mix of the products that are spotted on the array. Pooling part of the cDNA PCR products before they are printed and their subsequent amplification towards either sense or antisense cRNA provides an excellent common reference. Our results show that this reference yields a reproducible hybridization signal in 99.5% of the cDNA probes spotted on the array. Accordingly, a ratio can be calculated for every spot, and expression levels across different hybridizations can be compared. In dye-swap experiments this reference shows no significant ratio differences, with 95% of the spots within an interval of +/-0.2-fold change. The described method can be used in hybridizations with both amplified and non-amplified targets, is time saving and provides a constant batch of common reference that lasts for thousands of hybridizations.
机译:当将共同的参考文献共杂交到每个微阵列中时,比较不同cDNA微阵列实验中表达水平的比较容易。该参考文献通常由一个实验对照样品,一组细胞系或所有待分析样品的混合物组成。我们已经开发了一种替代性的通用参考文献,该参考文献由阵列中发现的多种产品组成。在打印之前,将部分cDNA PCR产物汇集起来,然后将其扩增为有义或反义cRNA,即可提供极好的通用参考。我们的结果表明,该参考可在阵列上发现的99.5%的cDNA探针中产生可再现的杂交信号。因此,可以为每个斑点计算比率,并且可以比较不同杂交之间的表达水平。在染料交换实验中,该参考文献未显示明显的比率差异,其中95%的斑点在+/- 0.2倍的变化范围内。所描述的方法可以用于与扩增的和未扩增的靶标的杂交中,既节省时间又提供了恒定批次的公共参考,其可持续进行数千次杂交。

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