Evidence map›Paper›PMID 42129090›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

In Vitro Selection of Antibodies by Ribosome Display.

He Huang, Xinran Gao, Guangbo Kang

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

He HuangDepartment of Biochemical Engineering, School of Chemical Engineering & Technology, Tianjin University, Tianjin, PR China. huang@tju.edu.cn.
Xinran GaoDepartment of Biochemical Engineering, School of Chemical Engineering & Technology, Tianjin University, Tianjin, PR China.
Guangbo KangDepartment of Biochemical Engineering, School of Chemical Engineering & Technology, Tianjin University, Tianjin, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribosome display is a powerful engineering research tool for the high-throughput selection of peptides or proteins, which results in the generation of high-performance binders against nearly any antigen of interest. As a cell-free display system, ribosome display has been well developed with many outstanding achievements for over 20 years. Compared with other related display techniques, ribosome display shows unique advantages and development prospects. This tool has been successfully exploited for the selection of functional and specific binders in vitro. Here, we describe methods for the construction and characterization of ribosome-displayed natural nanoantibody libraries, by which specific nanoantibody screening can be performed.

Indexed as

RibosomesSingle-Domain AntibodiesHumansPeptide LibraryPeptide LibrarySingle-Domain AntibodiesDisplay technologiesIn vitro selectionNanobodyRibosome display

Identifiers

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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.