分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

CRISPR/Cas12a-mediated Enzymatic recombinase amplification for rapid visual quantitative authentication of halal food

Xiaohui Wang, Wenyu Jin, Yao Yang, Huizi Ma, Honghong Liu, Jiawen Lei, Yuhua Wu, Li Zhang

Journal:ANALYTICA CHIMICA ACTA

IF:6.2

DOI:10.1016/j.aca.2023.341144

PMID:37032058

Published:2023-03-24

research field:分子生物学食品科学生物技术

Abstract

Economically motivated adulteration (EMA) has become a concern in food safety. We propose a CRISPR/ Ca s12a M ediated E nzymatic R ecombinase A mplification detection system (CAMERA) that integrates Enzymatic Recombinase Amplification (ERA) and Cas12a cleavage to detect halal food adulteration. We designed and screened crRNA targeting CLEC , a porcine-specific nuclear single-copy gene, and optimized the reagent concentrations and incubation times for the ERA and Cas12a cleavage steps. CAMERA was highly specific for pork ingredients detection. The DNA concentration and fluorescence signal intensity relationship was linear at DNA concentrations of 20–0.032 ng/μL. CAMERA detected as few as two CLEC copies and quantified samples with porcine DNA content as low as 5% within 25 min. The system could be operated in a miniaturized working mode that requires no technical expertise or professional equipment, making CAMERA a valuable tool in resource-limited areas for the qualitative and quantitative detection of pork ingredients in halal food.

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