脱氧核酶
污染
化学
清脆的
危险废物
铅(地质)
检出限
纳米技术
环境化学
色谱法
生物
生物化学
材料科学
生态学
古生物学
基因
作者
Ruijie Deng,Yaxuan Bai,Yumei Liu,Yunhao Lu,Zhifeng Zhao,Yi Deng,Hao Yang
摘要
Hazardous lead ions (Pb2+) even at a minute level can pose side effects on human health, highlighting the need for tools for trace Pb2+ detection. Herein, we present a DNAzyme-activated CRISPR assay (termed DzCas12T) for sensitive and one-pot detection of lead contamination. Using an extension-bridged strategy eliminates the need for separation to couple the DNAzyme recognition and CRISPR reporting processes. The tandem design endowed the DzCas12T assay with high specificity and sensitivity down to the pM-level. This assay has been used to detect lead contamination in food and water samples, indicating the potential for monitoring lead-associated environmental and food safety.
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