Evidence map›Paper›PMID 23680984›Full record

ArticleNature protocols2013

Creation of recombinant antigen-binding molecules derived from hybridomas secreting specific antibodies.

Conor Fields, David O'Connell, Sujing Xiao, Gil U Lee, Philippe Billiald, Julien Muzard

Abstract read
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In one paragraph

Article in Nature protocols, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Parasitology · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Article
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  13. Review
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

6 authors.

Conor FieldsUCD Centre for Nanomedicine, School of Chemistry and Chemical Biology, University College Dublin, Dublin, Ireland.
David O'Connell
Sujing Xiao
Gil U Lee
Philippe Billiald
Julien Muzard

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This protocol describes the design and development of recombinant monovalent antigen-binding molecules derived from monoclonal antibodies through rapid identification and cloning of the functional variable heavy (VH) and variable light (VL) genes and the design and cloning of a synthetic DNA sequence optimized for expression in recombinant bacteria. Typically, monoclonal antibodies are obtained from mouse hybridomas, which most often result from the fusion of B lymphocytes from immunized mice with murine myeloma cells. The protocol described here has previously been exploited for the successful development of multiple antibody-based molecules targeting a wide range of biomolecular targets. The protocol is accessible for research groups who may not be specialized in this area, and should permit the straightforward reverse engineering of functional, recombinant antigen-binding molecules from hybridoma cells secreting functional IgGs within 50 working days. Furthermore, convenient strategies for purification of antibody fragments are described.

Indexed as

Models, MolecularAnimalsAntibodies, MonoclonalCloning, MolecularHybridomasImmunoglobulin FragmentsImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsMiceRecombination, GeneticAntibodies, MonoclonalImmunoglobulin FragmentsImmunoglobulin Heavy ChainsImmunoglobulin Light Chains

Identifiers

PMID23680984

What OpenQuestion holds

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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.