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SAGE analysis from 1 microg of total RNA.

作者信息

Cai Jerry, Ash David, Jabs Ethylin Wang

机构信息

Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

Curr Protoc Cell Biol. 2002 Nov;Chapter 19:Unit 19.4. doi: 10.1002/0471143030.cb1904s16.

DOI:10.1002/0471143030.cb1904s16
PMID:18228401
Abstract

Serial analysis of gene expression (SAGE) is a powerful transcription-profiling method that allows simultaneous expression analysis of thousands of transcripts, provides absolute digital readout of the expression level, and identifies new genes. A disadvantage of SAGE is the relatively high amount of input RNA required. Consequently, several techniques have been developed to overcome this limitation, so that SAGE can be applied to very limited amounts of starting material, e.g., small biological samples such as tissue biopsies or microdissected materials. Here we describe a modified version of the original microSAGE protocol, which requires only 1 to 2 microg total RNA. This method avoids PCR amplification of cDNA and reamplification of ditags, procedures that potentially compromise the quantitative nature of this technique.

摘要

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