Evidence map›Paper›PMID 39503982›Full record

ArticleMolecular biology reports2024

Fluorescent primers amplification refractory mutation system qPCR (FP ARMS-qPCR) for MTHFR C677T SNP genotyping.

Yongjun Han, Hong Wu

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Visual Screening of Genetic Polymorphisms inSensors (Basel, Switzerland) · 2026
    Article
4 · The record

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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

2 authors.

Yongjun HanSecond School of Clinical Medicine, Henan University of Chinese Medicine, Zhengzhou, 450002, China.
Hong WuSecond School of Clinical Medicine, Henan University of Chinese Medicine, Zhengzhou, 450002, China. wuhong@hactcm.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe currently used methods for the detection of methylene tetrahydrofolic acid reductase (MTHFR) C677T single nucleotide polymorphism (SNP) are either time-consuming or expensive. In this study, we devised an accurate, rapid and easy-to-use SNP detection system based on fluorescent primers amplification refractory mutation system qPCR, known as FP ARMS-qPCR.

methodsFluorescent primers (FPs) modified by fluorescent dye or quencher near the 3' terminal thymine were designed. The reaction conditions were optimized and the performance was evaluated. Using commercial kits as controls, 242 samples were tested in parallel to verify the feasibility of the FP ARMS-qPCR assay.

resultsWe demonstrated the good sensitivity and specificity of the FP ARMS-qPCR with optimized conditions. The assay was able to accurately distinguish between different SNP sites of MTHFR C677T in less than 2 h using as low as 50 pg of template genomic DNA. Completely consistent genotyping results reveal that FP ARMS-qPCR is concordant with commercial kits.

conclusionWe established a specific, sensitive, and rapid FP ARMS-qPCR method for the detection of MTHFR C677T genotype. This could also serve as a potential diagnostic tool for a variety of diseases.

Indexed as

Genotyping TechniquesMethylenetetrahydrofolate Reductase (NADPH2)Polymorphism, Single NucleotideReal-Time Polymerase Chain ReactionDNA PrimersFluorescent DyesGenotypeHumansMutationSensitivity and SpecificityDNA PrimersFluorescent DyesMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanFolic acidFP ARMS-qPCRMelting curveMTHFR C677TSNP

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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.