Evidence map›Paper›PMID 42129100›Full record

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

Production of Antibody Fragments Suitable for 1:1, Site-Specific Labeling.

Urša Štrancar, Ario de Marco

Abstract read
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In one paragraph

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
–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

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

2 authors.

Urša ŠtrancarLaboratory of Environmental and Life Sciences, University of Nova Gorica, Nova Gorica, Slovenia.
Ario de MarcoLaboratory of Environmental and Life Sciences, University of Nova Gorica, Nova Gorica, Slovenia. ario.demarco@ung.si.ORCID http://orcid.org/0000-0001-7729-819X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunoreagents, such antibodies, must often be functionalized before being used for a specific application, and this modification can strongly affect their biophysical characteristics. In contrast, recombinant antibody fragments can be engineered with elevated precision at selected residues to obtain customized reagents. Several alternative strategies can be used that exploit different principles and require different effort to reach this objective. Direct labeling can be obtained by fusing the antibody fragment to a fluorescent protein; otherwise, tag sequences can be appended to the binders and then these are modified by chemical or enzymatic reactions. In this contribution, a model system will be illustrated and compared with other options to illustrate what factors should be considered to choose the functionalization strategy.

Indexed as

Immunoglobulin FragmentsProtein EngineeringStaining and LabelingAnimalsHumansRecombinant Fusion ProteinsImmunoglobulin FragmentsRecombinant Fusion ProteinsAviTagDerivatization tagsFluorescent proteinsFunctionalization strategyNon-canonical amino acidsRecombinant antibodies

Identifiers

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.