Evidence map›Paper›PMID 39229092›Full record

ArticlebioRxiv : the preprint server for biology2024

Ultraplex microscopy: versatile highly-multiplexed molecular labeling and imaging across scale and resolution.

Janeth Pérez-Garza, Jairo Orea, Zachary Deane, Gianna Raimondi, Rebecca Tripp, Imani Charles, Linnaea Ostroff

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

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

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

7 authors.

Janeth Pérez-GarzaDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.ORCID 0000-0002-3023-7741
Jairo OreaDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.
Zachary DeaneDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.ORCID 0009-0009-0223-3290
Gianna RaimondiDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.ORCID 0000-0002-2664-1362
Rebecca TrippDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.
Imani CharlesDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.
Linnaea OstroffDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Conn.ORCID 0000-0002-3348-342X

Funding

A versatile approach for highly multiplexed, high-resolution imaging of endogenous moleculesRF1MH130472 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI OSTROFF, LINNAEA E · 2022 to 2022
$2.2M
New strategies for molecular cell-type labeling in volume electron microscopyRF1MH129269 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI OSTROFF, LINNAEA E · 2022 to 2022
$1.1M
STED Super Resolution Microscope for a Core FacilityS10OD023618 · OD · UNIVERSITY OF CONNECTICUT STORRS · PI O'CONNELL, CHRISTOPHER B · 2018 to 2018
$1000k
Leica TCS SP8 FSU AOBS 405 UV Spectral Confocal MicroscopeS10OD016435 · OD · UNIVERSITY OF CONNECTICUT STORRS · PI NISHIYAMA, AKIKO · 2014 to 2014
$456k
NIH HHS S10 OD016435NIH HHS S10 OD023618NIMH NIH HHS RF1 MH129269NIMH NIH HHS RF1 MH130472
6 · The paper itself

Abstract

The molecular organization of cells and tissue is challenging to study due to the inefficiency of multiplexed molecular labeling methods and the limited options for combining microscopy modalities in a single specimen, especially when high spatial resolution is needed. Here we describe ultraplex microscopy, which combines serial multiplexing, ultrathin sectioning, and reversible embedding to circumvent incompatibilities between labeling and imaging techniques, enhance resolution, and expand multiplexing capacity within and across modalities. Samples can be labeled with antibodies, RNA probes, and tissue stains for imaging by brightfield, epifluorescence, super-resolution, and electron microscopy without specialized reagents or materials. We demonstrate applications in brain tissue including molecular profiling of single cells and axonal boutons, high-resolution molecular colocalization, and correlative imaging of fluorescent proteins with confocal and ultraplex microscopy. The power and versatility of ultraplex microscopy will be valuable in addressing currently intractable experimental questions in many systems and contexts.

Identifiers

PMID39229092
PMCPMC11370420

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.