Evidence map›Paper›PMID 20978962›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2011

Phage display: a powerful technology for the generation of high specificity affinity reagents from alternative immune sources.

William J J Finlay, Laird Bloom, Orla Cunningham

Abstract readReview
In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Antibody Affinity and Stability Maturation by Error-Prone PCR.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  4. Review
  5. Chicken antibodies against venom proteins ofThe journal of venomous animals and toxins including tropical diseases · 2020
    Article
  6. An update on antiviral antibody-based biopharmaceuticals.International immunopharmacology · 2020
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Inhibition of duck hepatitis B virus replication by mimic peptidesExperimental and therapeutic medicine · 2015
    Article
  12. Article
  13. Article
  14. 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

3 authors.

William J J FinlayWyeth Research Ireland, Dublin, Ireland.
Laird Bloom
Orla Cunningham

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies are critical reagents in many fundamental biochemical methods such as affinity chromatography. As our understanding of the proteome becomes more complex, demand is rising for rapidly generated antibodies of higher specificity than ever before. It is therefore surprising that few investigators have moved beyond the classical methods of antibody production in their search for new reagents. Despite their long-standing efficacy, recombinant antibody generation technologies such as phage display are still largely the tools of biotechnology companies or research groups with a direct interest in protein engineering. In this chapter, we discuss the inherent limitations of classical polyclonal and monoclonal antibody generation and highlight an attractive alternative: generating high specificity, high affinity recombinant antibodies from alternative immune sources such as chickens, via phage display.

Indexed as

Antibody SpecificityPeptide LibraryAnimalsAntibodiesChickensChromatography, AffinityHumansRecombinant ProteinsAntibodiesPeptide LibraryRecombinant Proteins

Identifiers

PMID20978962
PMCPMC7120213

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.