Evidence map›Paper›PMID 35517011›Full record

ArticleRSC advances2019

Ultrasensitive fluorescent aptasensor for CRP detection based on the RNase H assisted DNA recycling signal amplification strategy.

Zhongzhi Liu, Dan Luo, Fangling Ren, Fengying Ran, Wei Chen, Bingqiang Zhang, Ceming Wang, Hao Chen, Jian Wei, Qinhua Chen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in RSC advances, 2019. 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Zhongzhi LiuAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Dan LuoAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Fangling RenAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Fengying RanAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Wei ChenAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Bingqiang ZhangAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Ceming WangAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Hao ChenAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Jian WeiAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.
Qinhua ChenAffiliated Dongfeng Hospital, Hubei University of Medicine Hubei Shiyan 442008 China cqh77@163.com +86 0719 8272283.ORCID 0000-0002-9108-1314
Hubei University of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An aptamer-based method for the ultrasensitive fluorescence detection of C-reactive protein (CRP) was developed using the ribonuclease H (RNase H) assisted DNA recycling signal amplification strategy. In this assay, CRP can specifically bind to the aptamer of CRP and the DNA chain of P1 is released from the aptamer/P1 (Ap/P1) complexes. After the addition of the fluorescence labeled (5-FAM) RNA, P1 hybridizes with fluorescence labeled RNA to form a P1/RNA double strand. When RNase H is added, the RNA with fluorescence labeling in the double strand is specifically cut into nucleotide fragments, which cannot be adsorbed on the surface of the GO, so as to generate a fluorescence signal. In the absence of CRP, fluorescence labeled RNA cannot hybridize with P1 to form double strands, which is able to directly adsorb on the surface of GO, resulting in no fluorescence signal. The detection limit is as low as 0.01 ng mL

Identifiers

PMID35517011
PMCPMC9063470
OpenAlexW2938228806

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LicenceCC BY
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Registered trials

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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.