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Based on fluorescence quenching between guanine bases and fluorophore, a cost-effective biosensor for protein detection is developed.
In this paper, based on Guanine (G -quadruplex-thioflavin T (ThT) complex and terminal protection of small molecule-linked DNA, a simple and rapid biosensor for protein detection has been developed.
Toward this effort, high-sensitivity pH sensor with reasonable range (3 9) and selectivity biosensor for protein detection (available at 100 femtomolar concentration) have been achieved by MoS2-based FET [86].
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In this study, we developed a liposome-based, total internal reflection fluorescence, fiber-optic biosensor (TIRF-FOB) for protein detection, which integrates a liposomal amplifier and sandwich immunoassay format with TIRF-FOB.
In this paper, a fluorescent biosensor has been developed for protein detection based on poly(thymine) (poly T -templated copper nanoparT -templatedPs) and terminal protecopperof small molecule linanoparticles
The biosensor exhibits excellent analytical performance for protein detection in a range from 41.7 nM to 4.17 μM, with a detection limit of 4.17 nM.
Next, an investigation of the role of thin films of gold, silver, and aluminum for protein detection in SPR biosensors is presented.
The developed biosensor exhibits attractive performance for the analysis of SirT1, with rapid response, high sensitivity, and high accuracy, and could become a promising technique for protein detection.
Since the introduction by Gold et al. in 1990, nucleic acid aptamers had evolved to become a true contender in biosensors for protein and cell detections.
A plasmonic biosensor for rapid detection of protein biomarkers in complex media is reported.
This figure was reproduced from [34] Fig. 16 Showing schematic diagram of the SiNW biosensor for free detection of carbohydrate-protein interaction.
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