Evidence map›Paper›PMID 36971774›Full record

ArticleBiotechnology letters2023

Generation of a novel monoclonal antibody against inflammatory biomarker S100A8 using hybridoma technology.

Jong-Pyo Kim, Hanool Yun, Eun-Jung Kim, Yun-Gon Kim, Chang-Soo Lee, Byoung Joon Ko, Byung-Gee Kim, Hee-Jin Jeong

Abstract read
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In one paragraph

Article in Biotechnology letters, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

8 authors at 5 institutions in 1 country.

Jong-Pyo KimDepartment of Biological and Chemical Engineering, Hongik University, Sejong, 30016, Republic of Korea.
Hanool YunDepartment of Biological and Chemical Engineering, Hongik University, Sejong, 30016, Republic of Korea.
Eun-Jung KimBioMAX/N-Bio Institute, Seoul National University, Seoul, 08826, Republic of Korea.
Yun-Gon KimDepartment of Chemical Engineering, Soongsil University, Seoul, 06978, Republic of Korea.
Chang-Soo LeeDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon, 34134, Republic of Korea.
Byoung Joon KoSchool of Biopharmaceutical and Medical Sciences, Sungshin Women's University, Seoul, 02844, Republic of Korea.
Byung-Gee KimBioMAX/N-Bio Institute, Seoul National University, Seoul, 08826, Republic of Korea.
Hee-Jin JeongDepartment of Biological and Chemical Engineering, Hongik University, Sejong, 30016, Republic of Korea. heejinjeong@hongik.ac.kr.ORCID http://orcid.org/0000-0001-5897-1756
Hongik University · KRSeoul National University · KRChungnam National University · KRSoongsil University · KRSungshin Women's University · KR

Funding

Hongik University 2022 Hongik University Research FrontierKorea Forest Service (Korea Forestry Promotion Institute) R&D Program for Forest Science Technology 2022417A00-2223-AA02Korea Medical Device Development Fund KMDF_PR_20200901_0073National Research Foundation of Korea NRF-2017M3A9B6062989National Research Foundation of Korea NRF-2020R1I1A307411712
6 · The paper itself

Abstract

objectivesS100A8 is highly expressed in several inflammatory and oncological conditions. To address the current lack of a reliable and sensitive detection method for S100A8, we generated a monoclonal antibody with a high binding affinity to human S100A8 to enable early disease diagnosis.

resultsA soluble recombinant S100A8 protein with a high yield and purity was produced using Escherichia coli. Next, mice were immunized with recombinant S100A8 to obtain anti-human S100A8 monoclonal antibodies using hybridoma technology. Lastly, the high binding activity of the antibody was confirmed and its sequence was identified.

conclusionsThis method, including the production of antigens and antibodies, will be useful for the generation of hybridoma cell lines that produce anti-S100A8 monoclonal antibodies. Moreover, the sequence information of the antibody can be used to develop a recombinant antibody for use in various research and clinical applications.

Indexed as

Antibodies, MonoclonalCalgranulin AAnimalsBiomarkersCell LineHybridomasMiceRecombinant ProteinsAntibodies, MonoclonalBiomarkersCalgranulin ARecombinant ProteinsHybridoma technologyInflammationMonoclonal antibodyMRP8S100A8

Identifiers

PMID36971774
OpenAlexW4361017257

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.