Related Experiment Video
Updated: Jul 8, 2026

Field-Deployable Candidatus Liberibacter asiaticus Detection Using Recombinase Polymerase Amplification Combined with CRISPR-Cas12a
Published on: December 23, 2022
An "off-on" electrochemiluminescence biosensor based on CRISPR-Cas12a for ultrasensitive determination of aflatoxin
Zhi-Hong Xu1, Xiao Hu1, Xin Weng1
1College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, 350122, China. 2012029@fjtcm.edu.cn.
Abstract:
Accurate and sensitive determination of aflatoxin B1 (AFB1) is of vital importance for food safety. Herein, an electrochemiluminescence (ECL) "off-on" switch sensor combined with CRISPR-Cas12a is fabricated for the quantitative analysis of AFB1. Initially, the DNA activator is effectively locked by two AFB1 aptamers. Once the target AFB1 is introduced, the activator is released in an open state and thus is recognized by the Cas12a-crRNA duplex. Black hole quencher (BHQ)-marked DNA strands are digested by the activated CRISPR-Cas12a system. Owing to the resonance energy transfer (RET) between aggregation-induced ECL active (AIECL-active) polymer dots (Pdots) and BHQ, the ECL signal of Pdots switches from signal "off" to "on" along with the detachment of BHQ from the electrode surface. The proposed ECL sensor thus achieves sensitive quantification of AFB1 with a detection limit of 0.06 pg mL-1. This work provides an effective strategy for mycotoxin determination.
More Related Videos
07:59Rapid and Specific Detection of Acinetobacter baumannii Infections Using a Recombinase Polymerase Amplification/Cas12a-based System
Published on: April 25, 2025
06:47Combined Recombinase Polymerase Amplification CRISPR/Cas12a Assay for Detecting Fusarium oxysporum f. sp. cubense Tropical Race 4
Published on: November 14, 2025