研究目的
To develop a rapid, sensitive, and selective SERS-based lateral flow assay for the differential diagnosis of wild-type pseudorabies virus and gE-deleted vaccine.
研究成果
The SERS-based lateral flow assay is a rapid, sensitive, and specific method for the differential diagnosis of wild-type PRV and gE-deleted vaccine, with potential for clinical application.
研究不足
The method requires specific antibodies and nanoparticles, and the sensitivity might be affected by the quality of these materials.
1:Experimental Design and Method Selection:
Developed a SERS-based lateral flow assay using antigen-antibody reaction for the detection of wild-type PRV.
2:Sample Selection and Data Sources:
Used wild-type PRV, Bartha-K61 strain, and clinical samples for testing.
3:List of Experimental Equipment and Materials:
Included AuAg4-ATP@AgNPs, NC membrane, glass fiber membrane, and a portable Raman Spectrometer.
4:Experimental Procedures and Operational Workflow:
Prepared AuAg4-ATP@AgNPs, assembled the lateral flow strip, and performed detection with Raman spectroscopy.
5:Data Analysis Methods:
Analyzed Raman intensity at 1585.7 cm?1 for quantitative and semi-quantitative analysis.
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Transmission electron microscope
JEOL 2100F
JEOL
Used for the characterization of AuAg4-ATP@AgNPs
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Raman Spectrometer
RM-3000
Guangzhou Biaoqi Optoelectronics Technology Development Co., Ltd
Used to obtain detection signal
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NC membrane
HF13502S25
Millipore
Used as a detection pad
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Glass Fiber membrane
GF-08
Shanghai Jie Ning Biological Technology Co., Ltd
Used as a sample pad
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Centrifuge
5810 R
Eppendorf
Used to prepare the AuAg4-ATP@AgNPs
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Vortex Mixer
XW-80 A
Shanghai
Used to prepare the AuAg4-ATP@AgNPs
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PCR amplification apparatus
Eppendorf
Used to amplify DNA fragments
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Particle Size Analyzer
Malvern Instruments Ltd.
Used for the characterization of AuAg4-ATP@AgNPs
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Microplate Reader
Synergy H1 Hybrid Multi-Mode
Bio-Tek Instruments, Inc.
Used for the characterization of AuAg4-ATP@AgNPs
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