Fluorophore vendor resources: curated guide by manufacturer

Every major flow cytometry reagent vendor publishes dye-specific guides, spectrum viewers, and lot-specific COA data, but they're scattered across product pages that change URLs. This page curates the key resources by vendor and keeps them in one place.

How to use this page

Jump to a vendor using the filter below, or scroll through all of them. Each card links to the primary technical guides, spectrum viewers, and COA lookup tools for that vendor's dye families. URL paths can change; if a link is stale, search the vendor's site for the resource name.
BD

BD Biosciences

Brilliant Violet (BV)Brilliant UV (BUV)Brilliant Blue (BB)Brilliant Red (BR)+3 more

BD's Brilliant Stain portfolio is one of the largest in flow cytometry, covering violet, UV, blue, and red laser lines. Their spectrum viewer and the Brilliant Stain Buffer requirement (essential for panels with multiple BV dyes) are critical references.

Bi

BioLegend

SparkSpark BlueSpark Yellow-GreenPE/Fire series+2 more

BioLegend's Spark and Fire portfolios are designed as cross-laser-compatible polymer dyes with high brightness. Their Spectra Analyzer tool includes all Fire and Spark variants and is vendor-neutral enough to be useful for full panel planning.

Cy

Cytek Biosciences

cFluor YG seriescFluor B seriescFluor V seriescFluor R series

Cytek's cFluor dyes are optimized for their Aurora and Northern Lights full-spectrum instruments, though many work on conventional cytometers too. The naming convention encodes both laser (YG, B, V, R) and emission peak in the same name.

Bi

Bio-Rad

StarBright BlueStarBright VioletStarBright RedStarBright Yellow-Green

Bio-Rad's StarBright dyes are polymer-based high-brightness reagents designed with the laser color encoded in the name (StarBright Blue, Violet, Red, YG) and the emission peak as the number. They are primarily used on Bio-Rad's ZE5 cytometer but compatible with other platforms.

Mi

Miltenyi Biotec

VioBlueVioGreenVioBright FITCVioBright B515+3 more

Miltenyi's REAfinity and VioDye portfolios are designed for their MACSQuant instruments but work broadly on conventional cytometers. Vio dyes encode the laser in the color name (VioBlue = violet, VioBright = blue) and the emission in the number.

In

Invitrogen / Thermo Fisher

Alexa FluorPacific BluePacific OrangeSuperBright+2 more

Invitrogen (part of Thermo Fisher) originated the Alexa Fluor series and Pacific dyes, and continues the eBioscience eFluor and SuperBright lines. Alexa Fluors follow excitation-number convention, the most important difference from BV and SuperBright.

Pr

Proteintech

CoraLite Plus (CLP)

Proteintech's CoraLite Plus series are designed as direct drop-in substitutes for Alexa Fluors, following the same excitation-number convention. CLP647 is equivalent to AF647 and uses the same compensation settings.

Be

Beckman Coulter

SuperNovaKrome OrangeAlexa Fluor 700 (via license)PE-based tandems

Beckman Coulter's SuperNova and Krome Orange dyes are primarily optimized for their CytoFLEX instruments. Krome Orange (~528 nm, violet 405 nm) fills a unique spectral position not well covered by other brands.

Tips for evaluating vendor documentation

1

COA QC metrics ≠ spectral performance

Most vendor COAs report binding specificity; find independent emission spectra separately and don't assume a passing QC means good spectrum behavior.

2

Poster emission peaks are approximate

Vendor fluorochrome posters list nominal peaks, often rounded to 5–10 nm. Actual emission spectra are broader and may shift by a few nm across lots. Use the spectrum viewer, not the poster, for filter overlap decisions.

3

Brightness rankings are instrument-dependent

A dye ranked "brightest in class" on one laser/filter configuration may rank lower on your specific instrument. Always validate brightness with a titration on your own cytometer.

4

Technical guides often assume their own instruments

BD guides assume BD instruments; Cytek guides assume spectral cytometers. Adapt accordingly; a recommended filter from a vendor guide may not exist on your platform.

References

  • [1]Maecker HT, Frey T, Nomura LE, Trotter J. Selecting fluorochrome conjugates for maximum sensitivity. Cytometry A. 2004;62(2):169–73.
  • [2]Chattopadhyay PK, et al. A live-cell assay to detect antigen-specific CD4+ T cells with diverse cytokine profiles. Nat Med. 2005;11(10):1113–7.
  • [3]Perfetto SP, Chattopadhyay PK, Roederer M. Seventeen-colour flow cytometry: unravelling the immune system. Nat Rev Immunol. 2004;4(8):648–55.