z-logo
open-access-imgOpen Access
Microfluidics-based digital quantitative PCR for single-cell small RNA quantification†
Author(s) -
Tian Yu,
Chong Tang,
Ying Zhang,
Ruirui Zhang,
Wei Yan
Publication year - 2017
Publication title -
biology of reproduction
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.366
H-Index - 180
eISSN - 1529-7268
pISSN - 0006-3363
DOI - 10.1093/biolre/iox102
Subject(s) - biology , microrna , digital polymerase chain reaction , computational biology , real time polymerase chain reaction , microfluidics , rna , quantitative assessment , polymerase chain reaction , genetics , gene , nanotechnology , materials science , management , economics
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom