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AAT Bioquest

iFluor® 647 acid

AAT Bioquest's iFluor® dyes are optimized for labeling proteins, particularly antibodies. These dyes are bright, photostable, and have minimal quenching on proteins. They can be well excited by the major laser lines of fluorescence instruments (e.g., 350, 405, 488, 555, and 633 nm). The iFluor® 647 family has spectral properties essentially identical to those of Cy5®. Compared to Cy5® probes, iFluor® 647 reagents have much stronger fluorescence and higher photostability. Their fluorescence is pH-independent from pH 3 to 11. These spectral characteristics make this new dye family an excellent alternative to Cy5® and Alexa Fluor® 647 (Cy5® and Alexa Fluor® are the trademarks of GE Health Care and Invitrogen). 

iFluor® 647 acid is a non-reactive compound that can be employed as a reference standard in studies utilizing iFluor ® 647 conjugates. It is also suitable for use as a control in confocal microscopy, immunocytochemistry (ICC), high-content screening (HCS), flow cytometry, and live cell imaging applications. Furthermore, it can be utilized in the synthesis of activated esters and STP and can be coupled to hydrazines, hydroxylamines, or amines in aqueous solutions using water-soluble carbodiimides (e.g., EDAC). This allows for the conjugation of the dye to amino-containing molecules, such as proteins, antibodies, amine-modified oligonucleotides, and peptides.

Spectrum

Citations

View all 2 citations: Citation Explorer
A multistage drug delivery approach for colorectal primary tumors and lymph node metastases
Authors: Yuan, Yihang and Lin, Quanjun and Feng, Hai-Yi and Zhang, Yunpeng and Lai, Xing and Zhu, Mao-Hua and Wang, Jue and Shi, Jiangpei and Huang, Yanhu and Zhang, Lele and others,
Journal: Nature Communications (2025): 1439
Highly potent novel multi-armoured IL13R$\alpha$2 CAR-T subverts the immunosuppressive microenvironment of Glioblastoma
Authors: Mangolini, Maurizio and Srivastava, Saket and Souster, Emily and Yang, Yajing and Wang, Huimin and Karattil, Rajesh and Schultz, Liam and Ma, Biao and Pombal, Diana and Greenig, Matthew and others,
Journal: bioRxiv (2025): 2025--01
Page updated on April 15, 2025

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Catalog Number2909
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Physical properties

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.03

Correction Factor (280 nm)

0.03

Correction Factor (656 nm)

0.0793

Extinction coefficient (cm -1 M -1)

2500001

Excitation (nm)

656

Emission (nm)

670

Quantum yield

0.251

Storage, safety and handling

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

Storage

Freeze (< -15 °C); Minimize light exposure
With EDAC or other equivalent activating coupling agents, fluorescent dyes, such as iFluor® 647, can react readily with the primary amines (R-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.
With EDAC or other equivalent activating coupling agents, fluorescent dyes, such as iFluor® 647, can react readily with the primary amines (R-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.
With EDAC or other equivalent activating coupling agents, fluorescent dyes, such as iFluor® 647, can react readily with the primary amines (R-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.