Evidence map›Paper›PMID 34994225›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2022

Atto 465 Derivative Is a Nuclear Stain with Unique Excitation and Emission Spectra Useful for Multiplex Immunofluorescence Histochemistry.

Joshua T Dodge, Andrew D Doyle, Ana C Costa-da-Silva, Christopher T Hogden, Eva Mezey, Jacqueline W Mays

Open access · bronzeAbstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2022. 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
0.5field-weighted citation impact, top 23% of its field
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, 2 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Joshua T DodgeNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.ORCID 0000-0002-8029-2829
Andrew D DoyleNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.
Ana C Costa-da-SilvaNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.
Christopher T HogdenNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.
Eva MezeyNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.
Jacqueline W MaysNational Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland.ORCID 0000-0002-4472-9974
National Institutes of Health · US

Funding

Contribution of bone marrow cells to tissue regeneration, immune function and hematopoiesisZIADE000714 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI MEZEY, EVA M. · 2009 to 2025
$25.3M
Immunobiology and therapy of oral mucosal and salivary gland chronic graft-versus-host diseaseZIADE000747 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI MAYS, JACQUELINE · 2016 to 2025
$14.9M
6 · The paper itself

Abstract

Multiplex immunofluorescence (mIF) is an effective technique for the maximal visualization of multiple target proteins in situ. This powerful tool is mainly limited by the spectral overlap of the currently available synthetic fluorescent dyes. The fluorescence excitation wavelengths ranging between 405 and 488 nm are rarely used in mIF imaging and serve as a logical additional slot for a fluorescent probe. In the present study, we demonstrate that the addition of 2,3,4,5,6-pentafluoroaniline to Atto 465 NHS ester, creating Atto 465-pentafluoroaniline (Atto 465-p), generates a bright nuclear stain in the violet-blue region of the visible spectrum. This allows the 405 nm excitation and emission, classically used for nuclear counterstains, to be used for the detection of another target protein. This increases the flexibility of the mIF panel and, with appropriate staining and microscopy, enables the quantitative analysis of at least six targets in one tissue section.

Indexed as

Aniline CompoundsAnimalsCell NucleusFemaleFluorescent Antibody TechniqueFluorescent DyesFluorobenzenesFluorocarbonsHistocytochemistryMiceMice, Inbred BALB CProflavine2,3,4,5,6-pentafluoroanilineAniline CompoundsATTO 465Fluorescent DyesFluorobenzenesFluorocarbonsProflavineAtto 465immunofluorescenceimmunohistochemistrymultiplexnuclear stainphotoconversionphotostabilityproflavineSP8tyramide

Identifiers

PMID34994225
PMCPMC8832627
OpenAlexW4206665484

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.