Evidence map›Paper›PMID 16112641›Full record

ArticleBiochemical and biophysical research communications2005

Characterization and application of monoclonal antibodies against N protein of SARS-coronavirus.

Bo Shang, Xiao-Yi Wang, Jian-Wei Yuan, Astrid Vabret, Xiao-Dong Wu, Rui-Fu Yang, Lin Tian, Yong-Yong Ji, Vincent Deubel, Bing Sun

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

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  13. Structural insights into SARS-CoV-2 proteins.Journal of molecular biology · 2021
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Bo ShangLaboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institute of Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai 200031, China.
Xiao-Yi Wang
Jian-Wei Yuan
Astrid Vabret
Xiao-Dong Wu
Rui-Fu Yang
Lin Tian
Yong-Yong Ji
Vincent Deubel
Bing Sun

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome-coronavirus (SARS-CoV) causes an infectious disease through respiratory route. Diagnosing the disease effectively and accurately at early stage is essential for preventing the disease transmission and performing antiviral treatment. In this study, we raised monoclonal antibodies (mAbs) against the nucleocapsid (N) protein of SARS-CoV and mapped epitopes by using different truncated N protein fragments. The mapping of those epitopes was valuable for constructing pair-Abs used in serological diagnosis. The results showed that all of the six raised mAbs were divided into two groups recognizing the region of amino acids 249-317 (A group) or 317-395 (B group). This region spanning amino acids 249-395 contains predominant B cell epitopes located at the C-terminus of N protein. One pair-Abs, consisting of N protein-specific rabbit polyclonal antibody and SARS-CoV N protein-specific mAb, was selected to construct a sandwich ELISA-kit. The kit was able to specifically detect SARS-CoV N proteins in serum samples.

Indexed as

AnimalsAntibodies, MonoclonalCoronavirus Nucleocapsid ProteinsCross ReactionsElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayEpitopesHumansMiceMice, Inbred BALB CNucleocapsid ProteinsRabbitsSensitivity and SpecificitySevere Acute Respiratory SyndromeAntibodies, MonoclonalCoronavirus Nucleocapsid ProteinsEpitopesNucleocapsid Proteins

Identifiers

PMID16112641
PMCPMC7092910

What OpenQuestion holds

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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.