Evidence map›Paper›PMID 40601152›Full record

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

Alternative Matrices for Protein Biomarker Analysis by qPCR Using Proximity Extension Assay (PEA).

Adrián Llamas-Urbano, Julio Manuel Martínez-Moreno, Carlos Pérez-Sánchez, Nuria Barbarroja

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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

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

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.

Adrián Llamas-UrbanoCobiomic Bioscience SL, EBT UCO/IMIBIC, Cordoba, Spain.
Julio Manuel Martínez-MorenoCobiomic Bioscience SL, EBT UCO/IMIBIC, Cordoba, Spain.
Carlos Pérez-SánchezCobiomic Bioscience SL, EBT UCO/IMIBIC, Cordoba, Spain.
Nuria BarbarrojaCobiomic Bioscience SL, EBT UCO/IMIBIC, Cordoba, Spain. nuria@cobiomic.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advancements in proteomics and biomarker discovery require technologies capable of high-throughput, multiplexed, and minimally invasive protein detection. The Proximity Extension Assay (PEA), developed by Olink Proteomics, meets these demands by integrating dual-recognition immunoassays with quantitative PCR (qPCR), enabling the precise quantification of multiple proteins with exceptional sensitivity and specificity. While PEA is commonly applied to serum and plasma, its adaptability allows for the analysis of alternative biological matrices, including cerebrospinal fluid, urine, synovial fluid, bone marrow, amniotic fluid, blister fluid, conditioned media, interstitial fluid, and extracellular vesicles, among others. These matrices offer valuable opportunities for biomarker discovery, precision medicine, and translational research, particularly in diseases where conventional sampling is challenging. This chapter details the methodological considerations required for processing these alternative biofluids, ensuring their compatibility with PEA technology. It provides best practices for sample collection, processing, and quality control to maximize the accuracy and reproducibility of proteomic analyses. Additionally, it highlights PEA's ability to detect low-abundance proteins, which is critical for identifying novel biomarkers in complex biological samples.

Indexed as

BiomarkersProteinsProteomicsReal-Time Polymerase Chain ReactionHumansImmunoassayBiomarkersProteinsBiomarkersOlinkProtein arrayProteomicsProximity extension assayqPCR

Identifiers

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.