研究目的
To develop a FRET-based DNA sensor using an accumulated QD system for detecting KRAS G12D mutation, the most common mutation in cancer, enhancing the FRET signal and detection limit.
研究成果
The accumulated QD system on nanobeads significantly enhances the FRET signal and detection limit for KRAS G12D mutation, suggesting its potential as an ultrasensitive DNA nanosensor for cancer detection.
研究不足
The study may face challenges in enhancing the detection limit further and requires optimization for various cancer mutations.
1:Experimental Design and Method Selection:
The study utilized FRET-based nanosensors with QDs as donors and organic dyes as acceptors. The accumulated QD system was designed to enhance the FRET signal.
2:Sample Selection and Data Sources:
The target was KRAS G12D mutation DNA. The system included a capture probe, a reporter probe with Texas-red, and target DNA.
3:List of Experimental Equipment and Materials:
Cadmium oxide, zinc acetate, selenium, sulfur, trioctylphosphine, oleic acid, 1-octadecene, mercaptopropionic acid, adipic acid dihydrazide, tris-hydrochloride, ammonium sulfate, magnesium chloride, 2-(N-morpholino)ethanesulfonic acid, sodium chloride, sodium phosphate, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride, N-hydroxysulfosuccinimide, and 2-mercaptoethanol.
4:Experimental Procedures and Operational Workflow:
Synthesis of green color CdSe/CdZnS/ZnS QDs, modification of polystyrene beads with QDs, DNA hybridization, and FRET efficiency measurement.
5:Data Analysis Methods:
FRET efficiency and factor were calculated using fluorescence intensity measurements.
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