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PerCP-iFluor® 750

Product key features

  • Excitation/Emission Maxima: Efficient excitation at 488 nm with peak emission near 784 nm, enabling detection in the near-infrared region.
  • Low Spectral Overlap: Minimal spillover into adjacent channels facilitates cleaner separation in high-parameter flow cytometry panels.
  • High Signal Intensity: Delivers bright far-red fluorescence with excellent sensitivity and low background.
  • Large Stokes Shift: Enhances spectral resolution by maximizing the separation between excitation and emission wavelengths.

Product description

PerCP-iFluor® 750 is a tandem fluorophore engineered for high-parameter flow cytometry, providing strong far-red fluorescence with minimal spectral spillover. It comprises a peridinin chlorophyll protein (PerCP) donor covalently linked to an iFluor® 750 acceptor, allowing efficient energy transfer through Förster resonance energy transfer (FRET). Upon excitation with a 488 nm blue laser, the conjugate emits maximally near 784 nm, yielding a large Stokes shift and enabling sensitive detection in the near-infrared region. Its distinct spectral characteristics make PerCP-iFluor® 750 highly suitable for use in complex multicolor panels, where it helps minimize compensation and improves resolution of closely spaced populations. The dye is ideal for applications such as immunophenotyping, rare cell analysis, and other advanced flow cytometry workflows requiring high signal-to-noise ratios and precise population discrimination. PerCP-iFluor® 750 can be conjugated to proteins and antibodies using SMCC chemistry or through site-specific conjugation with Buccutite™ MTA and Buccutite™ FOL.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)
PerCP-iFluor® 700675707350000
PerCP-iFluor® 710719747350000
PerCP-iFluor® 720482747-
PerCP-iFluor® 780778806350000

References

View all 16 references: Citation Explorer
Routine flow cytometry approach for the evaluation of solid tumor neoplasms and immune cells in minimally invasive samples.
Authors: Quirós-Caso, Covadonga and Arias Fernández, Tamara and Fonseca-Mourelle, Ariana and Torres, Héctor and Fernández, Luis and Moreno-Rodríguez, Maria and Ariza-Prota, Miguel Ángel and López-González, Francisco Julián and Carvajal-Álvarez, Miguel and Alonso-Álvarez, Sara and Moro-García, Marco Antonio and Colado, Enrique
Journal: Cytometry. Part B, Clinical cytometry (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
The ISCCA flow protocol for the monitoring of anti-CD20 therapies in autoimmune disorders.
Authors: Gatti, Arianna and Buccisano, Francesco and Scupoli, Maria T and Brando, Bruno
Journal: Cytometry. Part B, Clinical cytometry (2021): 194-205
Comparison of minimal residual disease detection in multiple myeloma by SRL 8-color single-tube and EuroFlow 8-color 2-tube multiparameter flow cytometry.
Authors: Takamatsu, Hiroyuki and Yoroidaka, Takeshi and Fujisawa, Momoko and Kobori, Kazuya and Hanawa, Masako and Yamashita, Takeshi and Murata, Ryoichi and Ueda, Mikio and Nakao, Shinji and Matsue, Kosei
Journal: International journal of hematology (2019): 377-381
[Clinical features of imbalance between Th1 and Th22 cells and its association with disease progression in patients with liver cirrhosis].
Authors: Wu, H Q and Zhao, J J and Li, H W and Zhang, Z
Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology (2017): 738-744
Page updated on June 9, 2025

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Catalog Number2656
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Physical properties

Solvent

Water

Spectral properties

Excitation (nm)

482

Emission (nm)

784

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® 750 anti-human CD4 *SK3* conjugate. The fluorescence signal was monitored using an Aurora spectral flow cytometer in the PerCP-iFluor® 750 specific B14-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® 750 anti-human CD4 *SK3* conjugate. The fluorescence signal was monitored using an Aurora spectral flow cytometer in the PerCP-iFluor® 750 specific B14-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® 750 anti-human CD4 *SK3* conjugate. The fluorescence signal was monitored using an Aurora spectral flow cytometer in the PerCP-iFluor® 750 specific B14-A channel.