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Kai-Ren Zhao

Researcher at Jiangsu University

Publications -  14
Citations -  253

Kai-Ren Zhao is an academic researcher from Jiangsu University. The author has contributed to research in topics: Chemistry & Electrochemiluminescence. The author has an hindex of 4, co-authored 9 publications receiving 52 citations.

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Cas12a-based electrochemiluminescence biosensor for target amplification-free DNA detection.

TL;DR: Wang et al. as mentioned in this paper reported a novel Cas12a-based electrochemiluminescence biosensor for target amplification-free human papilloma virus subtype (HPV-16) DNA detection.
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Simple Tripedal DNA Walker Prepared by Target-Triggered Catalytic Hairpin Assembly for Ultrasensitive Electrochemiluminescence Detection of MicroRNA.

TL;DR: A simple enzyme-free target-triggered catalytic hairpin assembly (CHA) circuit was adopted to synthesize a tripedal DNA walker, which showed high selectivity and excellent reproducibility, demonstrating its practical application in bioanalysis.
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High luminous efficiency Au@CDs for sensitive and label-free electrochemiluminescent detection of circulating tumor cells in serum

TL;DR: In this paper, gold@carbon dots nanoalloys (Au@CDs) were synthesized by directly heating carbon dots and HAuCl4 aqueous solution to boiling.
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A dual-potential ratiometric electrochemiluminescence biosensor based on Au@CDs nanoflowers, Au@luminol nanoparticles and an enzyme-free DNA nanomachine for ultrasensitive p53 DNA detection

TL;DR: In this paper, an amplified electrochemiluminescence (ECL) ratiometric biosensor for p53 DNA sequence assay was described based on gold@carbon dots nanoflowers (Au@CDs), gold@luminol nanoparticles as luminophors and an enzyme-free DNA walker for signal amplification.
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A signal-switchable electrochemiluminescence biosensor based on the integration of spherical nucleic acid and CRISPR/Cas12a for multiplex detection of HIV/HPV DNAs

TL;DR: Using this strategy, HIV and HPV-16 DNAs are successfully quantitatively detection with detection limits of 30 fM and 0.32 pM (S/N = 3), respectively, and this system does not rely on multiplex signal reporting molecules, thus simplifying the detection system and avoiding the likelihood of cross interferences presented in the assay.