多路复用
多重聚合酶链反应
清脆的
生物
检出限
计算生物学
聚合酶链反应
化学
遗传学
色谱法
基因
作者
Gaihua Cao,Jiangbo Dong,Xiaolong Chen,Peng Lu,Yifan Xiong,Lan Peng,Jiawei Li,Danqun Huo,Changjun Hou
摘要
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.
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