Evidence map›Paper›PMID 40216722›Full record

ArticleDoklady. Biochemistry and biophysics2025

Development of an Anchor Bispecific Nanoantibody to Improve the Efficiency of Antigen Immobilization and Detection in a Well of a Polystyrene Plate.

S V Tillib, M V Panasyuk, O S Goryaynova, T I Ivanova

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Article in Doklady. Biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

4 authors.

S V TillibInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia. sergei.tillib@gmail.com.
M V PanasyukInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
O S GoryaynovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
T I IvanovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunoassay (IA) methods performed in the wells of a polystyrene microplate are the basis of diagnostic studies. In the "sandwich" IA, a fundamentally important initial stage is the immobilization of anchor antibodies in the well of the plate, designed for specific binding of a given antigen from a biological fluid. One of the very promising options for antigen-recognizing molecules are single-domain antibodies (nanoantibodies, Nbs). The use of Nbs as anchor antibodies is hampered by their low efficiency of functioning after passive adsorption in the well of the plate. The development of a new format and immobilization method in the case of Nbs are fundamentally important for overcoming this problem. This work describes the development of a new format of an anchor bispecific nanoantibody (anchor-Nb) to improve the efficiency of both passive adsorption of anchor-Nb and subsequent stages of immobilization and detection of the target antigen in the well of a polystyrene plate.

Indexed as

Antibodies, BispecificAntibodies, ImmobilizedAntigensPolystyrenesSingle-Domain AntibodiesHumansImmunoassayAntibodies, BispecificAntibodies, ImmobilizedAntigensPolystyrenesSingle-Domain Antibodiesbispecific antibodyimmunoassaynanoantibodynanobodysingle-domain antibody

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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.