| Literature DB >> 26721495 |
Samuel E Harvey1, Chonghui Cheng2.
Abstract
Quantification of alternative splicing to detect the abundance of differentially spliced isoforms of a gene in total RNA can be accomplished via RT-PCR using both quantitative real-time and semi-quantitative PCR methods. These methods require careful PCR primer design to ensure specific detection of particular splice isoforms. We also describe analysis of alternative splicing using a splicing "minigene" in mammalian cell tissue culture to facilitate investigation of the regulation of alternative splicing of a particular exon of interest.Entities:
Keywords: Alternative splicing; Minigene; RNA; RT-PCR; Splicing factors; Splicing regulation; Variable exon
Mesh:
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Year: 2016 PMID: 26721495 PMCID: PMC4770877 DOI: 10.1007/978-1-4939-3378-5_18
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745