Evidence map›Paper›PMID 24637158›Full record

ArticleAnalytical biochemistry2014

Modification of gel architecture and TBE/TAE buffer composition to minimize heating during agarose gel electrophoresis.

Brian A Sanderson, Naoko Araki, Jennifer L Lilley, Gilberto Guerrero, L Kevin Lewis

Abstract read
In one paragraph

Article in Analytical biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

19 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Heliyon · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. DifferentiationJournal of fungi (Basel, Switzerland) · 2021
    Article
  12. Article
  13. Article
  14. Horizontal Agarose Gel Mobility Shift Assay for Protein-RNA Complexes.Methods in molecular biology (Clifton, N.J.) · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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 at 1 institution in 1 country.

Brian A SandersonChemistry and Biochemistry, Texas State University, 601 University Drive, San Marcos, TX 78666, USA.
Naoko ArakiChemistry and Biochemistry, Texas State University, 601 University Drive, San Marcos, TX 78666, USA.
Jennifer L LilleyChemistry and Biochemistry, Texas State University, 601 University Drive, San Marcos, TX 78666, USA.
Gilberto GuerreroChemistry and Biochemistry, Texas State University, 601 University Drive, San Marcos, TX 78666, USA.
L Kevin LewisChemistry and Biochemistry, Texas State University, 601 University Drive, San Marcos, TX 78666, USA. Electronic address: LL18@txstate.edu.
Texas State University · US

Funding

Genome-wide analysis identifies genes required for repair of DNA strand breaksR15GM099049 · NIGMS · TEXAS STATE UNIVERSITY · PI LEWIS, LYSLE KEVIN · 2012 to 2012
$293k
NIGMS NIH HHS 1R15GM099049-01A1NIGMS NIH HHS R15 GM099049
6 · The paper itself

Abstract

Agarose gel electrophoresis of DNA and RNA is routinely performed using buffers containing either Tris, acetate, and EDTA (TAE) or Tris, borate, and EDTA (TBE). Gels are run at a low, constant voltage (∼10 V/cm) to minimize current and asymmetric heating effects, which can induce band artifacts and poor resolution. In this study, alterations of gel structure and conductive media composition were analyzed to identify factors causing higher electrical currents during horizontal slab gel electrophoresis. Current was reduced when thinner gels and smaller chamber buffer volumes were used, but was not influenced by agarose concentration or the presence of ethidium bromide. Current was strongly dependent on the amount and type of EDTA used and on the concentrations of the major acid-base components of each buffer. Interestingly, resolution and the mobilities of circular versus linear plasmid DNAs were also affected by the chemical form and amount of EDTA. With appropriate modifications to gel structure and buffer constituents, electrophoresis could be performed at high voltages (20-25 V/cm), reducing run times by up to 3-fold. The most striking improvements were observed with small DNAs and RNAs (10-100 bp): high voltages and short run times produced sharper bands and higher resolution.

Indexed as

Hot TemperatureAcetatesBoric AcidsDNAEdetic AcidElectrophoresis, Agar GelEthylenediaminesGelsTime FactorsTromethamineAcetatesBoric AcidsDNAEdetic AcidEthylenediaminesGelstris-acetate-EDTA bufferTris-borate-EDTA bufferTromethamineAgaroseCurrentGel electrophoresisNucleic acidsResolution

Identifiers

PMID24637158
PMCPMC4021863
OpenAlexW1996735213

What OpenQuestion holds

Textmetadata
LicenceTDM
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.