Evidence map›Paper›PMID 29161268›Full record

ArticlePLoS biology2017

Nucleic acid purification from plants, animals and microbes in under 30 seconds.

Yiping Zou, Michael Glenn Mason, Yuling Wang, Eugene Wee, Conny Turni, Patrick J Blackall, Matt Trau, Jose Ramon Botella

Erratum issuedAbstract read
In one paragraph

Article in PLoS biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 110 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed, 1 pooled it
–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

110 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Detection ofAnimals : an open access journal from MDPI · 2026
    Article
  4. Review
  5. Rapid On-Site Detection ofPlants (Basel, Switzerland) · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Revisions to theMycoKeys · 2026
    Article
  13. Material-to-Application Integration: Rapid Fabrication of Field-Deployable Hydrogel-SiOAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Super-Fast Detection ofFoods (Basel, Switzerland) · 2025
    Article
  20. Article

50 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Yiping ZouPlant Genetic Engineering Laboratory, School of Agriculture and Food Sciences, The University of Queensland, St.Lucia, Australia.
Michael Glenn MasonPlant Genetic Engineering Laboratory, School of Agriculture and Food Sciences, The University of Queensland, St.Lucia, Australia.ORCID http://orcid.org/0000-0001-5860-7989
Yuling WangCentre for Personalized Nanomedicine, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St.Lucia, Australia.
Eugene WeeCentre for Personalized Nanomedicine, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St.Lucia, Australia.
Conny TurniQueensland Alliance for Agriculture and Food Innovation, The University of Queensland, St.Lucia, Australia.
Patrick J BlackallQueensland Alliance for Agriculture and Food Innovation, The University of Queensland, St.Lucia, Australia.
Matt TrauCentre for Personalized Nanomedicine, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St.Lucia, Australia.
Jose Ramon BotellaPlant Genetic Engineering Laboratory, School of Agriculture and Food Sciences, The University of Queensland, St.Lucia, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleic acid amplification is a powerful molecular biology tool, although its use outside the modern laboratory environment is limited due to the relatively cumbersome methods required to extract nucleic acids from biological samples. To address this issue, we investigated a variety of materials for their suitability for nucleic acid capture and purification. We report here that untreated cellulose-based paper can rapidly capture nucleic acids within seconds and retain them during a single washing step, while contaminants present in complex biological samples are quickly removed. Building on this knowledge, we have successfully created an equipment-free nucleic acid extraction dipstick methodology that can obtain amplification-ready DNA and RNA from plants, animals, and microbes from difficult biological samples such as blood and leaves from adult trees in less than 30 seconds. The simplicity and speed of this method as well as the low cost and availability of suitable materials (e.g., common paper towelling), means that nucleic acid extraction is now more accessible and affordable for researchers and the broader community. Furthermore, when combined with recent advancements in isothermal amplification and naked eye DNA visualization techniques, the dipstick extraction technology makes performing molecular diagnostic assays achievable in limited resource settings including university and high school classrooms, field-based environments, and developing countries.

Indexed as

Genetic TechniquesAnimalsArabidopsisBacteriaCelluloseDNAHumansNucleic Acid Amplification TechniquesNucleic AcidsOligonucleotidesPlant LeavesPlantsRNACelluloseDNANucleic AcidsOligonucleotidesRNA

Identifiers

PMID29161268
PMCPMC5697807

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.