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PerCP-iFluor® 720

Product key features

  • Excitation/Emission: Excited at 488 nm with strong emission around 747 nm
  • High Photostability: More stable than traditional PerCP tandems, minimizing signal degradation
  • Low Spectral Spillover: Minimal interference with PE and APC channels in multicolor panels
  • High Sensitivity: Strong signal with low background in far-red channels

Product description

PerCP-iFluor® 720 is a tandem fluorophore specifically engineered for high-parameter flow cytometry applications. It consists of a peridinin chlorophyll protein (PerCP) donor covalently linked to an iFluor® 720 acceptor, enabling efficient energy transfer via Förster resonance energy transfer (FRET) upon excitation with a 488 nm blue laser. This results in a strong and well-defined emission peak near 747 nm, making it an ideal far-red reporter in multicolor panels.

The spectral characteristics of PerCP-iFluor® 720 allow for minimal spillover into adjacent channels, such as PE and APC, facilitating cleaner resolution in complex staining panels. Compared to traditional PerCP tandems, PerCP-iFluor® 720 exhibits enhanced photostability and higher signal-to-noise ratios, improving sensitivity for the detection of low-abundance targets. Its consistent performance across fixation and permeabilization conditions makes it suitable for both surface and intracellular staining protocols. PerCP-iFluor® 720 can be covalently linked to proteins and antibodies using SMCC (succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate) or site-specific Buccutite™ MTA and Buccutite™ FOL conjugation chemistries. Conjugation to antibodies or streptavidin further expands its utility in immunophenotyping, cell subset discrimination, and high-dimensional cytometry.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)
PerCP-iFluor® 700675707350000
PerCP-iFluor® 710719747350000
PerCP-iFluor® 750482784-
PerCP-iFluor® 780778806350000

References

View all 50 references: Citation Explorer
Single-Cell Sorting of Immunophenotyped Mesenchymal Stem Cells from Human Exfoliated Deciduous Teeth.
Authors: Gupta, Ayona and Mukhopadhyay, Risani and Khandelwal, Himanshi and Nala, Narendra and Chakraborty, Uttara
Journal: Journal of visualized experiments : JoVE (2023)
Development of constrictional microchannels and the recurrent neural network in single-cell protein analysis.
Authors: Zhang, Ting and Chen, Xiao and Chen, Deyong and Wang, Junbo and Chen, Jian
Journal: Frontiers in bioengineering and biotechnology (2023): 1195940
Whole blood no-lyse no-wash micromethod for the quantitative measurement of monocyte HLA-DR.
Authors: Miatello, Jordi and Faivre, Valérie and Marais, Clémence and Raineau, Mégane and Payen, Didier and Tissieres, Pierre
Journal: Cytometry. Part B, Clinical cytometry (2023)
Separation of Immune Cell Subpopulations in Peripheral Blood Samples from Children with Infectious Mononucleosis.
Authors: Zhang, Linlin and Liu, Mengjia and Zhang, Meng and Ai, Junhong and Tian, Jiao and Wang, Ran and Xie, Zhengde
Journal: Journal of visualized experiments : JoVE (2022)
Recombinant thrombomodulin attenuates hyper-inflammation and glycocalyx damage in a murine model of Streptococcus pneumoniae-induced sepsis.
Authors: Watanabe, Eizo and Akamatsu, Toshinobu and Ohmori, Masaaki and Kato, Mayu and Takeuchi, Noriko and Ishiwada, Naruhiko and Nishimura, Rintaro and Hishiki, Haruka and Fujimura, Lisa and Ito, Chizuru and Hatano, Masahiko
Journal: Cytokine (2022): 155723
Page updated on June 9, 2025

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Catalog Number2653
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Physical properties

Solvent

Water

Spectral properties

Excitation (nm)

482

Emission (nm)

747

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Refrigerated (2-8 °C); Minimize light exposure
Top) Spectral pattern was generated using a 4-laser spectral cytometer. Spatially offset lasers (355 nm, 405 nm, 488 nm, and 640 nm) were used to create four distinct emission profiles, then, when combined, yielded the overall spectral signature. Bottom) Flow cytometry analysis of whole blood stained with PerCP-iFlour® 720 anti-human CD4 *SK3* conjugate. The fluorescence signal was monitored using an Aurora spectral flow cytometer in the PerCP-iFluor® 720 specific B12-A channel.
Top) Spectral pattern was generated using a 4-laser spectral cytometer. Spatially offset lasers (355 nm, 405 nm, 488 nm, and 640 nm) were used to create four distinct emission profiles, then, when combined, yielded the overall spectral signature. Bottom) Flow cytometry analysis of whole blood stained with PerCP-iFlour® 720 anti-human CD4 *SK3* conjugate. The fluorescence signal was monitored using an Aurora spectral flow cytometer in the PerCP-iFluor® 720 specific B12-A channel.
Top) Spectral pattern was generated using a 4-laser spectral cytometer. Spatially offset lasers (355 nm, 405 nm, 488 nm, and 640 nm) were used to create four distinct emission profiles, then, when combined, yielded the overall spectral signature. Bottom) Flow cytometry analysis of whole blood stained with PerCP-iFlour® 720 anti-human CD4 *SK3* conjugate. The fluorescence signal was monitored using an Aurora spectral flow cytometer in the PerCP-iFluor® 720 specific B12-A channel.