Evidence map›Paper›PMID 38482358›Full record

ArticleAccess microbiology2024

A novel optimized pre-embedding antibody-labelling correlative light electron microscopy technique.

Nicole Doyle, Jennifer Simpson, Philippa C Hawes, Helena J Maier

Abstract read
In one paragraph

Article in Access microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Nicole DoyleThe Pirbright Institute, Ash Road, Pirbright, Woking, GU24 0NF, UK.ORCID https://orcid.org/0000-0002-6016-5830
Jennifer SimpsonThe Pirbright Institute, Ash Road, Pirbright, Woking, GU24 0NF, UK.
Philippa C HawesThe Pirbright Institute, Ash Road, Pirbright, Woking, GU24 0NF, UK.ORCID https://orcid.org/0000-0003-4665-9663
Helena J MaierThe Pirbright Institute, Ash Road, Pirbright, Woking, GU24 0NF, UK.ORCID https://orcid.org/0000-0002-2901-5578

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the intricate environment of a cell, many studies seek to discover the location of specific events or objects of interest. Advances in microscopy in recent years have allowed for high detail views of specific areas of cells of interest using correlative light electron microscopy (CLEM). While this powerful technique allows for the correlation of a specific area of fluorescence on a confocal microscope with that same area in an electron microscope, it is most often used to study tagged proteins of interest. This method adapts the correlative method for use with antibody labelling. We have shown that some cellular structures are more sensitive than others to this process and that this can be a useful technique for laboratories where tagged proteins or viruses, or dedicated CLEM instruments are not available.

Indexed as

antibody CLEMCLEMconfocal microscopycoronaviruscorrelativeCoVelectron microscopyreplication organelle

Identifiers

PMID38482358
PMCPMC10928386

What OpenQuestion holds

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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.