| Literature DB >> 29024970 |
Tian Yu1, Chong Tang1, Ying Zhang1, Ruirui Zhang1, Wei Yan1,2.
Abstract
Quantitative analyses of small RNAs at the single-cell level have been challenging because of limited sensitivity and specificity of conventional real-time quantitative PCR methods. A digital quantitative PCR (dqPCR) method for miRNA quantification has been developed, but it requires the use of proprietary stem-loop primers and only applies to miRNA quantification. Here, we report a microfluidics-based dqPCR (mdqPCR) method, which takes advantage of the Fluidigm BioMark HD system for both template partition and the subsequent high-throughput dqPCR. Our mdqPCR method demonstrated excellent sensitivity and reproducibility suitable for quantitative analyses of not only miRNAs but also all other small RNA species at the single-cell level. Using this method, we discovered that each sperm has a unique miRNA profile.Entities:
Keywords: RNA quantification; digital PCR; fertility; germ cells; small RNA; sperm
Mesh:
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Year: 2017 PMID: 29024970 PMCID: PMC6248614 DOI: 10.1093/biolre/iox102
Source DB: PubMed Journal: Biol Reprod ISSN: 0006-3363 Impact factor: 4.285