Evidence map›Paper›PMID 37457305›Full record

ArticleHardwareX2023

Versatile open-source fluorescence documentation system.

Leonhard Bandilla

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in HardwareX, 2023. 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Leonhard BandillaPfahlweg 18A, 82346 Andechs, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fluorescence has long been the best method for detecting bio-molecules at high sensitivity and with the possibility of easy data analysis and is routine for gel electrophoresis and much more. However, the systems for detecting the fluorophores remain expensive and thus inaccessible to many. Most commercial systems are often only optimized for one specific application, making reuse difficult. This paper demonstrates, characterizes and evaluates an inexpensive and versatile system for the detection of fluorophores with two wavelengths using high power LEDs. The LEDs are arranged in two banks angled downward at a tray in a way that allows for bright and uniform illumination while preventing direct reflections into the camera. The emitted light is filtered through an exchangeable filter frame and can be detected using the camera of a smartphone or similar device. By using filters both in front of the LEDs and the camera, very low background and using sufficient exposure times, very high sensitivity can be achieved. The two wavelengths of excitation light and the exchangeable filters allow for optimization for the specific fluorophore used and thus highest brightness.

Indexed as

Fluorescence imagingGel electrophoresisMacroscopic imagingOpen hardware

Identifiers

PMID37457305
PMCPMC10345341
OpenAlexW4382358235

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.