Evidence mapPaperPMID 39041865Full record

ArticleBiology open2024

Improved whole-mount immunofluorescence protocol for consistent and robust labeling of adult Drosophila melanogaster adipose tissue.

Rachael K Ott, Isaiah H Williams, Alissa R Armstrong

Abstract read
In one paragraph

Article in Biology open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Adipocyte-DerivedBiomolecules · 2025
    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

3 authors.

Rachael K OttDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29072, USA.
Isaiah H WilliamsDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29072, USA.
Alissa R ArmstrongDepartment of Biological Sciences, University of South Carolina, Columbia, SC 29072, USA.ORCID 0009-0004-8710-2831

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · TRUSTEES OF INDIANA UNIVERSITY · 2025 to 2025
$1.7M
Chan Zuckerberg Initiative 2022-253625NIH HHS P40 OD018537University of South Carolina
6 · The paper itself

Abstract

Energy storage and endocrine functions of the Drosophila fat body make it an excellent model for elucidating mechanisms that underlie physiological and pathophysiological organismal metabolism. Combined with Drosophila's robust genetic and immunofluorescence microscopy toolkits, studies of Drosophila fat body function are ripe for cell biological analysis. Unlike the larval fat body, which is easily removed as a single, cohesive sheet of tissue, isolating intact adult fat body proves to be more challenging, thus hindering consistent immunofluorescence labeling even within a single piece of adipose tissue. Here, we describe an improved approach to handling Drosophila abdomens that ensures full access of the adult fat body to solutions generally used in immunofluorescence labeling protocols. In addition, we assess the quality of fluorescence reporter expression and antibody immunoreactivity in response to variations in fixative type, fixation incubation time, and detergent used for cellular permeabilization. Overall, we provide several recommendations for steps in a whole-mount staining protocol that results in consistent and robust immunofluorescence labeling of the adult Drosophila fat body.

Indexed as

Adipose TissueDrosophila melanogasterFluorescent Antibody TechniqueAnimalsFat BodyMicroscopy, FluorescenceStaining and LabelingAdult fat bodyDrosophilaImmunofluorescence

Identifiers

PMID39041865
PMCPMC11317099

What Socratic holds

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Registered trials

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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 Socratic graph.