Evidence map›Paper›PMID 26132366›Full record

ArticleJournal of visualized experiments : JoVE2015

Transfecting RAW264.7 Cells with a Luciferase Reporter Gene.

Sylvia T Cheung, Soroush Shakibakho, Eva Y So, Alice L-F Mui

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Design andMaterials today. Bio · 2026
    Article
  2. Article
  3. Article
  4. Macrophage variants in laboratory research: most are well done, but some are RAW.Frontiers in cellular and infection microbiology · 2024
    Review
  5. FBXO11 constitutes a major negative regulator of MHC class II through ubiquitin-dependent proteasomal degradation of CIITA.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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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 at 1 institution in 1 country.

Sylvia T CheungImmunity and Infection Research Centre, Vancouver Costal Health Research Institute; Department of Surgery, University of British Columbia; Department of Biochemistry and Molecular Biology, University of British Columbia.
Soroush ShakibakhoImmunity and Infection Research Centre, Vancouver Costal Health Research Institute; Department of Surgery, University of British Columbia.
Eva Y SoImmunity and Infection Research Centre, Vancouver Costal Health Research Institute; Department of Surgery, University of British Columbia.
Alice L-F MuiImmunity and Infection Research Centre, Vancouver Costal Health Research Institute; Department of Surgery, University of British Columbia; Department of Biochemistry and Molecular Biology, University of British Columbia; alice.mui@ubc.ca.
University of British Columbia · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Transfection of desired genetic materials into cells is an inevitable procedure in biomedical research studies. While numerous methods have been described, certain types of cells are resistant to many of these methods and yield low transfection efficiency(1), potentially hindering research in those cell types. In this protocol, we present an optimized transfection procedure to introduce luciferase reporter genes as a plasmid DNA into the RAW264.7 macrophage cell line. Two different types of transfection reagents (lipid-based and polyamine-based) are described, and important notes are given throughout the protocol to ensure that the RAW264.7 cells are minimally altered by the transfection procedure and any experimental data obtained are the direct results of the experimental treatment. While transfection efficiency may not be higher compared to other transfection methods, the described procedure is robust enough for detecting luciferase signal in RAW264.7 without changing the physiological response of the cells to stimuli.

Indexed as

Genes, ReporterAnimalsCell LineLuciferasesMacrophagesMicePlasmidsTransfectionLuciferases

Identifiers

PMID26132366
PMCPMC4545129
OpenAlexW582856694

What OpenQuestion holds

Textmetadata
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.