Evidence map›Paper›PMID 30767050›Full record

ArticleHistochemistry and cell biology2019

Fluorescence microscope light source stability.

Firas Mubaid, Daniel Kaufman, Tse-Luen Wee, Dong-Son Nguyen-Huu, David Young, Maria Anghelopoulou, Claire M Brown

Abstract read
PubMed Publisher
In one paragraph

Article in Histochemistry and cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Tissue-Like 3D Standard and Protocols for Microscope Quality Management.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. In focus in HCB.Histochemistry and cell biology · 2019
    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

7 authors at 1 institution in 1 country.

Firas MubaidDepartment of Physiology, McGill University, Montreal, Canada.
Daniel KaufmanDepartment of Physiology, McGill University, Montreal, Canada.
Tse-Luen WeeDepartment of Physiology, McGill University, Montreal, Canada.
Dong-Son Nguyen-HuuDepartment of Anatomy and Cell Biology, McGill University, Montreal, Canada.
David YoungDepartment of Physics, McGill University, Montreal, Canada.
Maria AnghelopoulouDepartment of Chemical Engineering, McGill University, Montreal, Canada.
Claire M BrownDepartment of Physiology, McGill University, Montreal, Canada. claire.brown@mcgill.ca.
McGill University · CA

Funding

Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada 386084McGill University (CA) Sustainability Fund SP0149
6 · The paper itself

Abstract

The process of fluorescence starts with the efficient generation of light that is required for the excitation of fluorophores. As such, light sources are a crucial component of a fluorescence microscope. Choosing the right illumination tool can not only improve the quality of experimental results, but also the microscope's economic and environmental footprint. While arc lamps have historically proven to be a reliable light source for widefield fluorescence microscopy, solid-state light-emitting diodes (LEDs) have become the light source of choice for new fluorescence microscopy systems. In this paper, we demonstrate that LEDs have superior light stability on all timescales tested and use less electrical power than traditional light sources when used at lower power outputs. They can be readily switched on and off electronically, have a longer lifetime and they do not contain mercury, and thus are better for the environment. We demonstrate that it is important to measure light source power output during warm-up and switching, as a light source's responsiveness (in terms of power) can be quite variable. Several general protocols for testing light source stability are presented. A detailed life cycle analysis shows that an LED light source can have a fourfold lower environmental impact when compared to a metal halide source.

Indexed as

LightingMicroscopy, FluorescenceFluorescenceLEDLight sourceMicroscopySolid stateStability

Identifiers

PMID30767050
OpenAlexW2914627865

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.