Enhancing Flow Cytometry Multiplexing Panels with New StarBright™ Spectral Dyes 2259336

Abstract Introduction Full spectrum cytometry is increasingly preferred over conventional cytometry for its ability to generate data from larger, more complex panels. However, progress is hampered by the limited availability of suitable dyes. Many existing fluorophores are dim, have poor stability, lack a unique emission wavelength, or have high spectral overlap, limiting panel optimization and affecting data quality. Results Bio-Rad’s StarBright Dyes for flow cytometry have expanded to 36 fluorophores with the addition of four new Spectral StarBright Dyes, purpose-built for spectral cytometry, where no fluorophores with similar peak emissions exist. They address key challenges by providing bright, narrowly defined emission spectra, allowing larger panels to be acquired. Using data obtained from a Cytek Aurora (Cytek Biosciences), we show that these new dyes also enhance existing panels by replacing suboptimal traditional fluorophores, minimizing spectral overlap and spreading without compromising data quality Conclusion New Spectral StarBright Dyes provide the same benefits as current StarBright Dyes and are compatible with the existing dyes and other fluorophores, ensuring seamless integration into established workflows. The wide choice available simplifies panel design and offers alternatives for conventional dyes, offering improved performance while maintaining compatibility with standard protocols. Funding Source n/a Topic Categories Technological Innovations in Immunology (TECH)

Authors

Institutions

Publication Details

Journal
The Journal of Immunology
Published
2026-07-28
DOI
https://doi.org/10.1093/jimmun/vkag141.695
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Enhancing Flow Cytometry Multiplexing Panels with New StarBright™ Spectral Dyes 2259336

Lei Huang, Sharon Sanderson (91090), Michael Blundell, Ryan Mendoza et al.
The Journal of Immunology
Single-cell and spatial transcriptomics
article

Enhancing Flow Cytometry Multiplexing Panels with New StarBright™ Spectral Dyes 2259336

Lei Huang, Sharon Sanderson (91090), Michael Blundell, Ryan Mendoza, Tracey Long
article en

Abstract

Abstract Introduction Full spectrum cytometry is increasingly preferred over conventional cytometry for its ability to generate data from larger, more complex panels. However, progress is hampered by the limited availability of suitable dyes. Many existing fluorophores are dim, have poor stability, lack a unique emission wavelength, or have high spectral overlap, limiting panel optimization and affecting data quality. Results Bio-Rad’s StarBright Dyes for flow cytometry have expanded to 36 fluorophores with the addition of four new Spectral StarBright Dyes, purpose-built for spectral cytometry, where no fluorophores with similar peak emissions exist. They address key challenges by providing bright, narrowly defined emission spectra, allowing larger panels to be acquired. Using data obtained from a Cytek Aurora (Cytek Biosciences), we show that these new dyes also enhance existing panels by replacing suboptimal traditional fluorophores, minimizing spectral overlap and spreading without compromising data quality Conclusion New Spectral StarBright Dyes provide the same benefits as current StarBright Dyes and are compatible with the existing dyes and other fluorophores, ensuring seamless integration into established workflows. The wide choice available simplifies panel design and offers alternatives for conventional dyes, offering improved performance while maintaining compatibility with standard protocols. Funding Source n/a Topic Categories Technological Innovations in Immunology (TECH)

The Journal of ImmunologyVol. 215(Supplement_1)
Bio-Rad (United States) (US)
Industry, innovation and infrastructure
Openalex Percentile: Top 15%
Single-cell and spatial transcriptomics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.