Evidence map›Paper›PMID 32306067›Full record

ArticleAnalytical and bioanalytical chemistry2020

Ultrasensitive cloth-based microfluidic chemiluminescence detection of Listeria monocytogenes hlyA gene by hemin/G-quadruplex DNAzyme and hybridization chain reaction signal amplification.

Qiuping Shang, Yan Su, Yi Liang, Wei Lai, Jun Jiang, Hongyang Wu, Chunsun Zhang

Erratum issuedAbstract read
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In one paragraph

Article in Analytical and bioanalytical chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 42 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Qiuping Shang *MOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China.
Yan Su *MOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China.
Yi Liang *MOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China.
Wei LaiMOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China.
Jun JiangMOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China.
Hongyang WuMOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China.
Chunsun ZhangMOE Key Laboratory of Laser Life Science & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, No. 55, Zhongshan Avenue West, Tianhe District, Guangzhou, 510631, Guangdong, China. zhangcs@scnu.edu.cn.
South China Normal University · CN

Funding

Guangdong Basic and Applied Basic Research Foundation 2019A1515011284National Natural Science Foundation of China 81571765
6 · The paper itself

Abstract

In this work, a cloth-based chemiluminescence (CL) biosensor has been firstly presented for highly sensitive determination of long PCR amplicons. Under the action of a hybridization chain reaction, a good deal of hemin/G-quadruplex DNAzyme molecules are produced, which can effectively enhance the CL signal. Moreover, effective cloth-based DNA biosensors can be fabricated by sequential wax screen-printing and surface-modification processes. Especially, the integration of a desirable hydrophobic barrier and gravity/capillary flow onto the flow channel of the cloth-based device makes the biosensor easy to be fabricated and to be associated with a flow CL. For the luminol/H

Indexed as

G-QuadruplexesAnimalsBacterial ToxinsBiosensing TechniquesDNA, BacterialDNA, CatalyticHeat-Shock ProteinsHeminHemolysin ProteinsListeria monocytogenesListeriosisLuminescent MeasurementsMicrofluidic Analytical TechniquesMilkNucleic Acid HybridizationBacterial ToxinsDNA, BacterialDNA, CatalyticHeat-Shock ProteinsHeminHemolysin ProteinshlyA protein, Listeria monocytogenesChemiluminescenceCloth-based microfluidicsDetection of pathogenic bacteriaDNA biosensorHemin/G-quadruplex DNAzymeHybridization chain reaction

Identifiers

PMID32306067
OpenAlexW3016281662

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.