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用于小样本中多个基因表达分析的多重标准化逆转录聚合酶链反应

Multiplex standardized RT-PCR for expression analysis of many genes in small samples.

作者信息

Crawford Erin L, Warner Kristy A, Khuder Sadik A, Zahorchak Robert J, Willey James C

机构信息

Department of Medicine, Medical College of Ohio, 3055 Arlington Ave., Toledo, OH 43699, USA.

出版信息

Biochem Biophys Res Commun. 2002 Apr 26;293(1):509-16. doi: 10.1016/S0006-291X(02)00243-7.

Abstract

Standardized RT-PCR (StaRT-PCR) enables numerical quantification as well as intra- and inter-laboratory comparison of gene expression. Multiplex StaRT-PCR, using two rounds of amplification, was conducted on Stratagene Universal Reference RNA. In the first round, cDNA, competitive template (CT) mix, and primers for up to 96 genes were amplified for varying numbers of cycles. Next, products from round one were diluted, combined with primers for one gene, and amplified for an additional 35 cycles. No additional cDNA or CT mix was added. Expression values obtained by uniplex and multiplex StaRT-PCRs were highly correlated (R=0.993, p<0.001). Products from round one could be diluted as much as 100,000-fold and still be quantified following round two amplification. Thus, using multiplex StaRT-PCR, 96 genes were measured in the same amount of cDNA typically used to measure one gene with uniplex StaRT-PCR. Multiplex StaRT-PCR was also used to measure 18 genes in the fine needle biopsy of a primary lung carcinoma.

摘要

标准化逆转录聚合酶链反应(StaRT-PCR)能够实现基因表达的定量分析以及实验室内部和实验室之间的比较。使用两轮扩增的多重StaRT-PCR在Stratagene通用参考RNA上进行。在第一轮中,对cDNA、竞争性模板(CT)混合物和多达96个基因的引物进行不同循环数的扩增。接下来,将第一轮的产物稀释,与一个基因的引物混合,并再扩增35个循环。不添加额外的cDNA或CT混合物。单重和多重StaRT-PCR获得的表达值高度相关(R = 0.993,p < 0.001)。第一轮的产物可以稀释多达100,000倍,并且在第二轮扩增后仍可定量。因此,使用多重StaRT-PCR,在通常用于单重StaRT-PCR测量一个基因的相同量的cDNA中测量了96个基因。多重StaRT-PCR还用于测量原发性肺癌细针穿刺活检中的18个基因。

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