Evidence map›Paper›PMID 20382151›Full record

ArticleJournal of immunological methods2010

Isolation of scFv fragments specific for monokine induced by interferon-gamma (MIG) using phage display.

Edward Eteshola

Abstract read
In one paragraph

Article in Journal of immunological methods, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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

8 citing papers in PubMed, 21 citations in OpenAlex.

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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

1 author at 1 institution in 1 country.

Edward EtesholaDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH 43230, USA. Edward.Eteshola@osumc.edu
The Ohio State University · US

Funding

Protein Engineering and Biosensing Interface MaterialsK01EB004960 · NIBIB · OHIO STATE UNIVERSITY · PI ETESHOLA, EDWARD · 2005 to 2009
$708k
NIBIB NIH HHS EB004960NIBIB NIH HHS K01 EB004960
6 · The paper itself

Abstract

Iterative affinity selection procedures were used to isolate a number of single chain Fv (scFv) antibody fragment clones from naïve Tomlinson I+J phage display libraries that specifically recognize and bind a chemokine, monokine induced by interferon-gamma (MIG/CXCL9). MIG is an important transplant rejection/biology chemokine protein. ELISA-based affinity characterization results indicate that selectants preferentially bind to MIG in the presence of key biopanning component materials and closely related chemokine proteins. These novel antibody fragments may find utility as molecular affinity interface receptors in various electrochemical biosensor platforms to provide specific MIG binding capability with potential applications in transplant rejection monitoring, and other biomedical applications where detection of MIG level is important.

Indexed as

Peptide LibraryAmino Acid SequenceBinding, CompetitiveChemokine CXCL9ChemokinesCross ReactionsElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayEpitopesEscherichia coliHumansMolecular Sequence DataRecombinant ProteinsSingle-Chain AntibodiesChemokine CXCL9ChemokinesCXCL9 protein, humanEpitopesPeptide LibraryRecombinant ProteinsSingle-Chain Antibodies

Identifiers

PMID20382151
PMCPMC2925400
OpenAlexW1975213915

What OpenQuestion holds

Textmetadata
LicenceTDM
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.