Stears R L, Getts R C, Gullans S R
Brigham and Women's Hospital, Department of Medicine, Harvard Institutes of Medicine, Boston, Massachusetts 02115, USA.
Physiol Genomics. 2000 Aug 9;3(2):93-9. doi: 10.1152/physiolgenomics.2000.3.2.93.
To improve signal detection on cDNA microarrays, we adapted a fluorescent oligonucleotide dendrimeric signal amplification system to microarray technology. This signal detection method requires 16-fold less RNA for probe synthesis, does not depend on the incorporation of fluorescent dNTPs into a reverse transcription reaction, generates a high signal-to-background ratio, and can be used to allow for multichannel detection on a single chip. Furthermore, since the dendrimers can be detected individually, it may be possible, by employing dendrimer-binding standards, to calculate the numbers of bound cDNAs can be estimated. These features make the dendrimer signal detection reagent ideal for high-throughput functional genomics research.
为了提高cDNA微阵列上的信号检测,我们将一种荧光寡核苷酸树枝状信号放大系统应用于微阵列技术。这种信号检测方法在探针合成时所需的RNA量减少了16倍,不依赖于荧光dNTP掺入逆转录反应,产生高信噪比,并且可用于在单个芯片上进行多通道检测。此外,由于可以单独检测树枝状聚合物,通过使用树枝状聚合物结合标准物,有可能估计结合的cDNA数量。这些特性使树枝状聚合物信号检测试剂成为高通量功能基因组学研究的理想选择。