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用于DNA微阵列的新型多重5'-氨基修饰引物。

Novel multiple 5'-amino-modified primer for DNA microarrays.

作者信息

Han Jing, Lee Hin, Nguyen Nga Yen, Beaucage Serge L, Puri Raj K

机构信息

Laboratory of Molecular Tumor Biology, Division of Cellular and Gene Therapies, Bethesda, MD 20892, USA.

出版信息

Genomics. 2005 Aug;86(2):252-8. doi: 10.1016/j.ygeno.2005.04.009.

Abstract

For DNA microarray analysis, total RNA is reverse-transcribed, labeled by incorporating fluorescent dye into the cDNA, and used to hybridize microarray. This protocol requires a minimum of 20 microg of total RNA. To overcome the sample limitation, an RNA amplification technique has been developed. Although it needs less RNA, this amplification technique is relatively expensive, time consuming, and, unfortunately, has been found to introduce bias. In this study, we designed a novel 5'-amino-modified primer and used it for priming cDNA synthesis. The novel primer has a special structure that contains four Uni-Link molecules with two nucleotide (thymine) residues inserted between them as spacers. This novel primer is used in the reverse-transcription reaction for cDNA synthesis. Using the novel 5'-modified primer combined with indirect labeling method, cDNA probes can be prepared with much less total RNA (5 microg or less) without amplification producing optimal results after hybridization of arrays. This primer can also be used to label nucleotides for other purposes.

摘要

对于DNA微阵列分析,总RNA先进行逆转录,通过将荧光染料掺入cDNA进行标记,然后用于与微阵列杂交。该方案至少需要20微克总RNA。为克服样本限制,已开发出一种RNA扩增技术。尽管该扩增技术所需RNA较少,但相对昂贵、耗时,且不幸的是,已发现其会引入偏差。在本研究中,我们设计了一种新型的5'-氨基修饰引物,并将其用于引发cDNA合成。这种新型引物具有特殊结构,包含四个单链连接分子,它们之间插入了两个核苷酸(胸腺嘧啶)残基作为间隔。这种新型引物用于逆转录反应以合成cDNA。使用新型5'-修饰引物结合间接标记法,可在不进行扩增的情况下,用少得多的总RNA(5微克或更少)制备cDNA探针,阵列杂交后产生最佳结果。该引物还可用于标记核苷酸以用于其他目的。

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