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Simultaneous detection of CaMV35S and T-nos utilizing CRISPR/Cas12a and Cas13a with multiplex-PCR (MPT-Cas12a/13a).

Gaihua CaoJiangbo DongChangjun HouPeng LuYifan XiongLan PengJiawei LiDanqun HuoChangjun Hou
Published in: Chemical communications (Cambridge, England) (2022)
Here, we established a strategy (MPT-Cas12a/13a) that combined CRISPR/Cas12a and Cas13a for simultaneously detecting CaMV35S and T-nos based on multiplex PCR (M-PCR) and transcription. It realized a simultaneous detection mode with different signals in the same space. The MPT-Cas12a/13a had excellent sensitivity with the limit of detection as low as 11 copies of T-nos and 13 copies of CaMV35S and it had outstanding specificity and anti-interference ability in actual sample analysis. Therefore, it is a potential candidate in the detection of GM crops.
Keyphrases
  • crispr cas
  • genome editing
  • real time pcr
  • loop mediated isothermal amplification
  • label free
  • nitric oxide synthase
  • transcription factor
  • risk assessment