| Literature DB >> 19272451 |
Zhen Wang1, James Tollervey, Michael Briese, Daniel Turner, Jernej Ule.
Abstract
UV cross-linking and immunoprecipitation assay (CLIP) can identify direct interaction sites between RNA-binding proteins and RNAs in vivo, and has been used to study several proteins in tissues and cell cultures. The main challenge of the method is to specifically amplify the low amount of isolated RNA. The current protocol is optimised for efficient RNA purification and ligation of barcoded RNA adapters. High-throughput sequencing of the multiplexed cDNA library allows for a comprehensive coverage of the target sequences.Entities:
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Year: 2009 PMID: 19272451 DOI: 10.1016/j.ymeth.2009.02.021
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608