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Integrating recombinase polymerase amplification with CRISPR/Cas9-initiated nicking-rolling circle amplification in Staphylococcus aureus assay.

Jiang-Guo XuTong ZhouDanni XueZhuqi SuiHaidong YangXinyue YuanQi Wang
Published in: Chemical communications (Cambridge, England) (2024)
We integrate recombinase polymerase amplification (RPA) with CRISPR/Cas9-initiated nicking rolling circle amplification (CRISPR/Cas9-nRCA) for detecting Staphylococcus aureus . This approach utilizes a unique dimeric G-triplex structure, demonstrating firstly enhanced ThT fluorescence for target detection. The proof-of-concept study introduces a new avenue for integrating isothermal amplifications with CRISPR/Cas9 in the fields of pathogen detection and disease diagnosis.
Keyphrases
  • crispr cas
  • genome editing
  • nucleic acid
  • staphylococcus aureus
  • label free
  • loop mediated isothermal amplification
  • biofilm formation
  • high throughput
  • real time pcr
  • single molecule
  • candida albicans
  • single cell