FluoProbes


title: "FluoProbes" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["dyes", "fluorescent-dyes"] topic_path: "general/dyes" source: "https://en.wikipedia.org/wiki/FluoProbes" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

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Fluorescent dyeColormass (g/mol)Absorb (nm)Emit (nm)ε (M−1cm−1)
FluoProbes 390violet34339047924 000
FluoProbes 488green80449351985 000
FluoProbes 532yellow765532553117 000
FluoProbes547Horange736557574150 000
FluoProbes 594red1137601627120 000
FluoProbes647Hfar-red761653674250 000
FluoProbes 682far-red853690709140 000
FluoProbes 752near-IR879748772270 000
FluoProbes 782near-IR976783800170 000
Abs = absorption maximum#, Em = emission maximum# ..................................
ε = molar extinction coefficient
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The FluoProbes series of fluorescent dyes were developed by Interchim to improve performances of standard fluorophores. They are designed for labeling biomolecules, cells, tissues or beads in advanced fluorescent detection techniques.

  • FluoProbes dyes are typically used to label proteins or nucleic acids (ultrafast -3 minutes- labeling of antibodies employs Lightning technology). Labeled products can be used for multiparameter detections, life time resolved fluorescence (TRF), polarisation anisotropy fluorescence, FRET, Quenching, FRAP. They are typically used in biotechnology and research applications as fluorescence microscopy, cell biology or molecular biology, as well as infrared imaging. Derivatives with Amine and Carboxyl suit peptide and nucleic acid synthesis, while reactive ones (with succinimidyl, maleimide and hydrazide) suit conjugation by conventional chemistry, while FluoProbes labeled antibodies and cellular probes (i.e. Phalloidin) suit direct use in immunoassays or cell assays.
  • FluoProbes dyes that have comparable excitation and emission spectra to standard fluorophores such as fluoresceins, rhodamines, cyanines Cy2/3/5/5.5/7, are claimed to solve limiting issues observed in some applications such as too high background, insufficient polarity, photobleaching, insufficient brightness, or pH-sensitivity. I.e., FluoProbes488 reduces the background in Flow Cytometry and in slide microscopy allowing sharper and brighter images. FluoProbes 488, 547H and 647H are found more photostable that is taken to good account in applications using long illuminations periods (i.e. scanning such as in confocal microscopy), or for longer shelf-life of reagents (i.e. manufacturing diagnostics).

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FluoProbes dyeColorLight sources (spectral line)
FluoProbes 390violetDiode laser
FluoProbes 488
Fluorescein(FITC)/Cy2cyanArgon laser (488.0nm), Krypton laser (482.5nm)
FluoProbes 532yellowHelium–neon laser (632.8nm)
FluoProbes 547H
TRITC/Cy3orangeArgon laser (528.7nm)
FluoProbes 594
SR101/TRredArgon laser (528.7nm)
FluoProbes 647H
Cy5far redKrypton laser (647.1nm), Laser (633nm)
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Similar lines of fluorescent dyes provide an alternative to the FluoProbes Dyes.

References

References

  1. (2010). "FluoProbes Dyes". Interchim.
  2. [http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WSN-4KD4PVT-V-1&_cdi=7051&_user=10&_pii=S0092867406007616&_orig=search&_coverDate=07%2F14%2F2006&_sk=998739998&view=c&wchp=dGLzVtb-zSkWz&md5=e87c56b7f1f6f88e80896b600ae3a4ea&ie=/sdarticle.pdf Article] Savina A. ; Cell 126, 205–218, July 14, 2006 (Phagosome Neutrality in Host Defense)
  3. "Lightning technology from Innova BioSciences".
  4. [http://www.mcponline.org/content/6/6/1007.full.pdf+htm Article] Brunner ; Molecular & Cellular Proteomics 2007, 6.6, pp.1007-1017
  5. [https://www.interchim.fr/ft/B/BH4140.pdf AnnexinV-FluoProbes488 comparison in FCM]
  6. [https://www.interchim.fr/ft/B/BB052a.pdf FluoProbes labeling agent]
  7. [https://www.interchim.fr/ft/F/FP488c.pdf FluoProbes488 comparison to FITC, Cyanine2]
  8. [https://www.interchim.fr/ft/F/FP547c.pdf FluoProbes547H comparison in Confocal Microscopy]
  9. (2010). "FluoProbes Dyes". Interchim.

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