Evidence map›Paper›PMID 38968413›Full record

ArticleThe journal of physical chemistry. B2024

Analysis of Fluorescent Proteins for Observing Single Gene Locus in a Live and Fixed

Jung Bae Son, Seunghyeon Kim, Sora Yang, Youmin Ahn, Nam Ki Lee

Abstract read
In one paragraph

Article in The journal of physical chemistry. B, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Direct Quantification of Protein-Protein Interactions in Living Bacterial Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    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

5 authors.

Jung Bae SonDepartment of Chemistry, Seoul National University, 08826 Seoul, South Korea.
Seunghyeon KimDepartment of Chemistry, Seoul National University, 08826 Seoul, South Korea.
Sora YangDepartment of Chemistry, Seoul National University, 08826 Seoul, South Korea.
Youmin AhnDepartment of Chemistry, Seoul National University, 08826 Seoul, South Korea.
Nam Ki LeeDepartment of Chemistry, Seoul National University, 08826 Seoul, South Korea.ORCID 0000-0002-6597-555X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescent proteins (FPs) are essential tools for advanced microscopy techniques such as super-resolution imaging, single-particle tracking, and quantitative single-molecule counting. Various FPs fused to DNA-binding proteins have been used to observe the subcellular location and movement of specific gene loci in living and fixed bacterial cells. However, quantitative assessments of the properties of FPs for gene locus measurements are still lacking. Here, we assessed various FPs to observe specific gene loci in live and fixed

Indexed as

Escherichia coliLuminescent ProteinsGenetic LociMicroscopy, FluorescenceRepressor ProteinsLuminescent ProteinsRepressor Proteins

Identifiers

PMID38968413
PMCPMC11264270

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.