WeChat Mini Program
Old Version Features
Activate VIP¥0.73/day
Master AI Research

Amplification-free Quantitative Detection of Genomic DNA Using Lateral Flow Strips for Milk Authentication.

BIOSENSORS & BIOELECTRONICS(2024)

Chinese Acad Agr Sci

Cited 4|Views21
Abstract
With the globalization and complexity of the food supply chain, the market is becoming increasingly competitive and food fraudulent activities are intensifying. The current state of food detection faced two primary challenges. Firstly, existing testing methods were predominantly laboratory-based, requiring complex procedures and precision instruments. Secondly, there was a lack of accurate and efficient quantitative detection methods. Taking cow's milk as an example, this study introduced a novel method for nucleic acid quantification in dairy products, based on lateral flow strips (LFS). The core idea of this method is to design single-stranded DNA (ssDNA) probes to hybridize with mitochondrial genes, which are abundant, stable, and species-specific in dairy products, as detection targets. Drawing inspiration from the principles of nucleic acid amplification, this research innovatively established a new DNA hybridization method, named LAMP-Like Hybridization (HybLAMP-Like). Leveraging the denaturation and DNA polymerization functions of the bst enzyme, efficient binding of the probe and template strand was achieved. This method eliminated the need for nucleic acid amplification, simplifying the procedure and mitigating aerosol contamination, thereby ensuring the accuracy of the detection results. The method exhibited exceptional sensitivity, capable of detecting extremely low to 12.5 ng in visual inspection and 3.125 ng when using a reader. In terms of practicality, it could achieve visual detection of cow's milk content as low as 1% in adulterated dairy products. When combined with a portable LFS reader, it also enabled precise quantitative analysis of milk adulteration.
More
Translated text
Key words
Food authenticity,Free-amplification,DNA hybridization,Lateral flow strips,Quantitative detection
上传PDF
Bibtex
收藏
AI Read Science
AI Summary
AI Summary is the key point extracted automatically understanding the full text of the paper, including the background, methods, results, conclusions, icons and other key content, so that you can get the outline of the paper at a glance.
Example
Background
Key content
Introduction
Methods
Results
Related work
Fund
Key content
  • Pretraining has recently greatly promoted the development of natural language processing (NLP)
  • We show that M6 outperforms the baselines in multimodal downstream tasks, and the large M6 with 10 parameters can reach a better performance
  • We propose a method called M6 that is able to process information of multiple modalities and perform both single-modal and cross-modal understanding and generation
  • The model is scaled to large model with 10 billion parameters with sophisticated deployment, and the 10 -parameter M6-large is the largest pretrained model in Chinese
  • Experimental results show that our proposed M6 outperforms the baseline in a number of downstream tasks concerning both single modality and multiple modalities We will continue the pretraining of extremely large models by increasing data to explore the limit of its performance
Upload PDF to Generate Summary
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Data Disclaimer
The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn
Chat Paper

要点】:本研究提出了一种无需扩增的牛乳认证方法,通过侧流条检测技术(LFS)和LAMP-Like杂交方法实现了对牛奶中核苷酸的定量检测。

方法】:通过设计能与牛奶中丰富的、稳定的、物种特异性的线粒体基因杂交的单链DNA(ssDNA)探针,利用bst酶的变性和DNA聚合功能实现了高效探针-模板链结合,无需进行核苷酸扩增。

实验】:实验使用了牛乳样本,通过侧流条实现了对牛奶含量的视觉检测,低至1%的掺假乳制品即可被检测出,且在配合便携式LFS读取器时,能够进行精确的定量分析。实验中未明确提到具体的数据集名称,但结果显示方法在视觉检查中能检测低至12.5 ng的DNA,使用读取器时能检测至3.125 ng。