Evidence map›Paper›PMID 26175430›Full record

ArticleMethods in cell biology2015

Correlative light and electron microscopy analysis of the centrosome: A step-by-step protocol.

Dong Kong, Jadranka Loncarek

Abstract read
In one paragraph

Article in Methods in cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  4. Review
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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

2 authors.

Dong KongLaboratory of Protein Dynamics and Signaling, NIH/NCI/CCR-Frederick, Frederick, MD, USA.
Jadranka LoncarekLaboratory of Protein Dynamics and Signaling, NIH/NCI/CCR-Frederick, Frederick, MD, USA.

Funding

Control of centrosome biogenesisZIABC011459 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LONCAREK, JADRANKA · 2012 to 2025
$16.1M
Intramural NIH HHS ZIA BC011459
6 · The paper itself

Abstract

Correlative light and electron microscopy harnesses the best from each of the two modalities of microscopy it utilizes; while light microscopy provides information about the dynamic properties of the cellular structure or fluorescently labeled protein, electron microscopy provides ultrastructural information in an unsurpassed resolution. However, tracing a particular cell and its rare and small structures such as centrosomes throughout numerous steps of the experiment is not a trivial task. In this chapter, we present the experimental workflow for combining live-cell fluorescence microscopy analysis with classical transmission electron microscopy, adapted for the studies of the centrosomes and basal bodies. We describe, in a step-by-step manner, an approach that can be affordably and successfully employed in any typical cell biology laboratory. The article details all key phases of the analysis starting from cell culture, live-cell microscopy, and sample fixation, through the steps of sample preparation for electron microscopy, to the identification of the target cell on the electron microscope.

Indexed as

CentrosomeHeLa CellsHumansMicroscopy, Electron, TransmissionMicroscopy, FluorescenceMicrotomyPlastic EmbeddingStaining and LabelingCentrioleCentrosomeCorrelative light and electron microscopy (CLEM)Live-cell microscopySerial sectioning

Identifiers

PMID26175430
PMCPMC7711276

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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.