研究目的
The development of a cost-effective, sensitive, and selective detection method for identifying and monitoring foodborne pathogens to improve public health.
研究成果
The HRPzyme-integrated PCR-based colorimetric method is simple, sensitive, and selective for the detection of foodborne pathogens, with potential applications in resource-limited areas.
研究不足
The method requires PCR amplification, which may not be feasible in all settings, and the specificity is dependent on the primer design.
1:Experimental Design and Method Selection:
The study employs HRPzyme-integrated PCR for the colorimetric detection of foodborne pathogens, utilizing PC-based ImageJ software for data analysis.
2:Sample Selection and Data Sources:
Various foodborne pathogens including E. coli O157:H7, B. cereus, L. monocytogenes, and V. parahaemolyticus were used.
3:List of Experimental Equipment and Materials:
DNA polymerase (Tth), DNA Ladder, oligonucleotides, hemin, ABTS, 10X TBE buffer, PBS, citrate buffer, agarose.
4:Experimental Procedures and Operational Workflow:
PCR amplification of 16S rRNA sequences specific to foodborne pathogens without genomic DNA isolation, followed by colorimetric signal generation and analysis using ImageJ software.
5:Data Analysis Methods:
Color intensities were measured, quantified, and averaged from three experiments using ImageJ software.
独家科研数据包,助您复现前沿成果,加速创新突破
获取完整内容