| Literature DB >> 29256243 |
Samuel C Kim1, Iain C Clark1, Payam Shahi1, Adam R Abate1,2,3.
Abstract
Droplet microfluidics can identify and sort cells using digital reverse transcription polymerase chain reaction (RT-PCR) signals from individual cells. However, current methods require multiple microfabricated devices for enzymatic cell lysis and PCR reagent addition, making the process complex and prone to failure. Here, we describe a new approach that integrates all components into a single device. The method enables controlled exposure of isolated single cells to a high pH buffer, which lyses cells and inactivates reaction inhibitors but can be instantly neutralized with RT-PCR buffer. Using our chemical lysis approach, we distinguish individual cells' gene expression with data quality equivalent to more complex two-step workflows. Our system accepts cells and produces droplets ready for amplification, making single-cell droplet RT-PCR faster and more reliable.Entities:
Mesh:
Year: 2018 PMID: 29256243 PMCID: PMC5991602 DOI: 10.1021/acs.analchem.7b04050
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986