Talanta, Год журнала: 2024, Номер 285, С. 127384 - 127384
Опубликована: Дек. 14, 2024
Язык: Английский
Talanta, Год журнала: 2024, Номер 285, С. 127384 - 127384
Опубликована: Дек. 14, 2024
Язык: Английский
Clinica Chimica Acta, Год журнала: 2025, Номер 569, С. 120179 - 120179
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
2Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 161110 - 161110
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
2Microchemical Journal, Год журнала: 2025, Номер unknown, С. 113581 - 113581
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
1Sensors and Actuators B Chemical, Год журнала: 2024, Номер 418, С. 136253 - 136253
Опубликована: Июль 4, 2024
Язык: Английский
Процитировано
6Journal of Agricultural and Food Chemistry, Год журнала: 2024, Номер 72(15), С. 8831 - 8839
Опубликована: Апрель 4, 2024
Here, we present a method for Salmonella detection using clustered regularly interspaced short palindromic repeats associated with the CRISPR-associated protein 12a-hybridization chain reaction (CRISPR/Cas12a-HCR) system combined polymerase reaction/recombinase-assisted amplification (PCR/RAA) technology. The approach relies on invA gene as biorecognition element and its through PCR RAA. In presence of target gene, Cas12a, guided by crRNA, recognizes cleaves product, initiating HCR. Fluorescently labeled single-stranded DNA (ssDNA) H1 H2 were introduced, concentration was determined based fluorescence intensity from triggered Both assays demonstrate high specificity, sensitivity, simplicity, rapidity. range 2 × 101–2 109 CFU/mL, an LOD 20 entire process enabled specific rapid within 85–105 min. Field-incurred spiked recovery tests conducted in mutton beef samples both assays, demonstrating satisfactory accuracy animal-derived foods. By combining CRISPR/Cas12a hybridization technology, this study presents sensitive that is crucial identifying pathogenic bacteria monitoring food safety.
Язык: Английский
Процитировано
5Talanta, Год журнала: 2024, Номер 279, С. 126665 - 126665
Опубликована: Авг. 3, 2024
Язык: Английский
Процитировано
4International Journal of Biological Macromolecules, Год журнала: 2024, Номер 276, С. 133884 - 133884
Опубликована: Июль 14, 2024
Язык: Английский
Процитировано
3Sensors and Actuators B Chemical, Год журнала: 2024, Номер unknown, С. 137120 - 137120
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
3Elsevier eBooks, Год журнала: 2025, Номер unknown, С. 181 - 213
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0Analytical Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Фев. 25, 2025
Ruthenium(II) complexes with special ligands have been widely recognized in numerous fields and attributed to their outstanding DNA binding capacity. Hybridization chain reaction (HCR), as an enzyme-free amplification technique, forms long double-stranded (dsDNA) structures, which provides intercalation platform for these obtains effective enhancement of luminescent signals a significant extent enhances the sensitivity detection. Hence, Ru(dip)2(tpphz) [dip = 4,7-diphenyl-1,10-phenanthroline, tpphz tetrapyrido[3,2-a:2′,3′-c:3″,2″-h:2‴,3‴-j]phenazine] confirmed possess high capacity via UV–vis absorption spectroscopy AutoDock theoretical simulation calculations was synthesized luminescence probe. As proof concept, label-free ECL/PL dual-mode biosensor further constructed. In this design, magnetic silica spheres trigger were amplified by HCR hairpin DNA, forming large amounts dsDNA on surface, incorporated generate robust signals. Trigger cleaved owing activation Cas12a cleavage ability presence target, disappeared, reduced. The exhibited selectivity, LOD low 69 fM (S/N 3). results proved that has excellent ECL PL dual properties, huge potential establish biosensors simultaneously offers tremendous prospect anticancer, gene therapy, molecular probes beyond future.
Язык: Английский
Процитировано
0