Evidence map›Paper›PMID 41627761›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Expansion Microscopy in Euglenozoa.

Marie Zelená, Anežka Konupková, Vladimír Hampl, Vladimír Varga

Abstract read
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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Marie ZelenáLaboratory of Cell Motility, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Anežka KonupkováDepartment of Parasitology, Faculty of Science, BIOCEV, Charles University, Vestec, Czech Republic.
Vladimír HamplDepartment of Parasitology, Faculty of Science, BIOCEV, Charles University, Vestec, Czech Republic.
Vladimír VargaLaboratory of Cell Motility, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic. vladimir.varga@img.cas.cz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Expansion microscopy is a powerful technique, which increases the effective resolution of a fluorescence microscope by physically enlarging the specimen within a swellable polymer matrix. When combined with confocal microscopy, it enables affordable and easy-to-implement super-resolution imaging of protein localization in an entire cellular volume. Here, we describe in detail a protocol for the expansion of Euglenozoa, such as Trypanosoma brucei and Euglena gracilis, which achieves an average expansion factor of 4.6 in the case of T. brucei and 3.5 in the case of E. gracilis. This method is compatible with a broad range of available antibodies targeting endogenous proteins or small epitope tags. Additionally, we demonstrate the use of a fluorescent NHS ester for whole-proteome staining, BODIPY lipid stain, and the SYTOX nucleic acid stain for reproducible DNA labeling in expanded cells of these organisms. These reagents further increase the versatility of this simple yet robust super-resolution approach for studies of the cell biology of Euglenozoa.

Indexed as

Euglena gracilisEuglenozoaTrypanosoma brucei bruceiMicroscopy, ConfocalMicroscopy, FluorescenceStaining and LabelingChloroplastCytoskeletonEuglena gracilisExpansion microscopyMitochondrionSuper-resolution light microscopyTrypanosoma brucei

Identifiers

PMID41627761

What OpenQuestion 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 OpenQuestion graph.