Evidence map›Paper›PMID 40418474›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Measurement of DNA Polymerase and Microhomology-Mediated End-Joining Activities by Gel Electrophoresis and smFRET Techniques.

Yubin Sung, Chanwoo Kim, Hajin Kim, Kei-Ichi Takata

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yubin SungCenter for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea.
Chanwoo KimDepartment of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea.
Hajin KimDepartment of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea. hajinkim@unist.ac.kr.
Kei-Ichi TakataCenter for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea. ktakata@ibs.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA replication mediated by DNA polymerases is important not only for replicating genomic DNA but also for repairing damaged DNA. Elucidating the function of each DNA polymerase is essential for understanding how genomic integrity is maintained. Here, we present two types of DNA polymerase assays: one is the conventional method using sequence gel and the other is the single-molecule Förster resonance energy transfer (smFRET) measurement. The conventional method is sensitive and suitable for detecting the end product of DNA replication. On the other hand, the smFRET assay can monitor the intermediate stages of the reaction such as the synapsis between two single-stranded DNAs (ssDNAs). The two assays complement each other and provide information for more detailed analysis when used together.

Indexed as

DNA-Directed DNA PolymeraseDNA End-Joining RepairFluorescence Resonance Energy TransferDNA ReplicationDNA, Single-StrandedSingle Molecule ImagingDNA-Directed DNA PolymeraseDNA, Single-StrandedDNA polymerase assayDNA polymerase θMicrohomology-mediated end-joiningPOLQsmFRET

Identifiers

PMID40418474

What OpenQuestion holds

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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.