Liang Xue

TL;DR: The trans-cleavage activity of CRISPR/Cas12a is introduced into an electrochemical biosensor (E-CRISPR), combined with recombinase-assisted amplification (RAA), to establish a cost-effective, specific and ultrasensitive method; namely RAA-based E-CRisPR.

TL;DR: Novel viruses were found to cover major categories of RNA viruses, and many formed novel clusters divergent from the previously described taxa, dramatically broadening the range of known RNA viruses in insects.

TL;DR: In this article, the authors proposed a CRISPR/Cas12a-based fluorescence detection platform named Cas12aFDet for rapid nucleic acid detection that overcomes the timeconsuming process and the risk of aerosol contamination during DNA amplicon transfer.

TL;DR: In this article, a novel CRISPR/Cas12a-based fluorescence enhanced lateral flow biosensor (LFB) with functionalized quantum dots, combined with recombinase-assisted amplification (RAA), was used to detect Staphylococcus aureus.

TL;DR: It was demonstrated that C. jejuni could make more biofilm in aerobic conditions than in microaerobic conditions, and only 13.9% C.Jejuni entered coccus (a VBNC state) under microaer aerobic conditions; however, the rate increased to 95.5% under aerobic conditions.