| Literature DB >> 15131340 |
Fredrik Kamme1, Jessica Zhu, Lin Luo, Jingxue Yu, Da-Thao Tran, Bernhard Meurers, Anton Bittner, Karin Westlund, Susan Carlton, Jackson Wan.
Abstract
Generating gene-expression profiles from laser-captured cells requires the successful combination of laser-capture microdissection, RNA extraction, RNA amplification, and microarray analysis. To permit single-cell gene-expression profiling, the RNA amplification method has to be sufficiently powerful to bridge the gap between the amount of RNA available from a single cell to what is required by the microarray, a gap that spans 5 to 6 orders of magnitude. This chapter focuses on the amplification of RNA using a two-round T7 RNA amplification method. The protocols described are adapted for laser-captured material and have been used to generate gene expression profiles from single laser-captured cells.Mesh:
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Year: 2004 PMID: 15131340 DOI: 10.1385/1-59259-770-X:215
Source DB: PubMed Journal: Methods Mol Med ISSN: 1543-1894