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AAT Bioquest

XFD635 NHS Ester

Product key features

  • Ex/Em: 633/647 nm
  • Extinction Coefficient: 140,000 cm-1M-1
  • Reactive Group: NHS ester
  • Easy Conjugation: Efficiently labels primary amines on proteins, ligands, and amine-modified oligonucleotides
  • Advanced Dye Properties: Excellent water solubility and structural match to Alexa Fluor™ 635
  • Robust Signal Performance: Maintains high intensity and pH independence (pH 4-11) with exceptional photostability

Product description

XFD635, manufactured by AAT Bioquest, is a bright far red-fluorescent dye structurally identical to Alexa Fluor™ 635 (ThermoFisher). It is characterized by its intense brightness, high fluorescence quantum yield and photostability. The dye demonstrates excellent solubility in aqueous solutions and retains pH-independent fluorescence over a broad range (pH 4–11), ensuring consistent performance across diverse experimental conditions. Optimally excited by the 633 nm emission line of He-Ne lasers or the 635 nm diode laser, XFD635 is particularly well-suited for flow cytometry. Its robust and uniform labeling properties yield high signal intensity and reproducibility, making it an ideal choice for advanced fluorescence imaging, flow cytometry, and various fluorescence-based analytical techniques.

The N-hydroxysuccinimidyl (NHS) ester of XFD635 is a widely used reagent for the conjugation of this dye to proteins or antibodies. NHS esters react selectively and efficiently with primary amines (such as the side chains of lysine residues or aminosilane-coated surfaces) at pH 7-9, forming stable covalent amide bonds. This property makes XFD635 NHS ester an excellent choice for labeling proteins, amine-modified oligonucleotides, and other amine-containing molecules.

Spectrum

References

View all 50 references: Citation Explorer
The parasympathetic and sensory innervation of the proximal and distal colon in male mice.
Authors: Wang, Lixin and Taché, Yvette
Journal: Frontiers in neuroanatomy (2024): 1422403
Retinal Input to Macaque Superior Colliculus Derives from Branching Axons Projecting to the Lateral Geniculate Nucleus.
Authors: Zheng, Yicen J and Adams, Daniel L and Gentry, Thomas N and Dilbeck, Mikayla D and Economides, John R and Horton, Jonathan C
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience (2024)
Total Flavonoids of Polygala fallax Hemsl Induce Apoptosis of Human Ectopic Endometrial Stromal Cells through PI3K/AKT/Bcl-2 Signaling Pathway.
Authors: Zhong, Chuanmei and Ju, Gongchenhao and Yang, Sufang and Zhao, Xiangpei and Chen, Jixiang and Li, Ning
Journal: Gynecologic and obstetric investigation (2023): 197-213
Resolving arteriolar wall structures in mouse brain in vivo with three-photon microscopy.
Authors: Qin, Mengyuan and Huang, Jie and Zhong, Jincheng and Zhang, Yingxian and Tong, Shen and Cheng, Hui and Deng, Xiangquan and Zheng, Lei and Zhang, Wanjian and Qiu, Ping and Wang, Ke
Journal: Journal of biophotonics (2023): e202200365
Diyne inactivators and activity-based fluorescent labeling of phenol hydroxylase in Pseudomonas sp. CF600.
Authors: Oyarzun Mejia, Alejandra P and Hyman, Michael R
Journal: FEMS microbiology letters (2023)
Page updated on April 15, 2025

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Catalog Number70081
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Physical properties

Solvent

DMSO

Spectral properties

Extinction coefficient (cm -1 M -1)

140,000

Excitation (nm)

633

Emission (nm)

647

Storage, safety and handling

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

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501
Schematic illustrating the NHS ester–amine coupling between an NHS ester‐activated dye and an amine‐modified biomolecule. NHS esters react readily with lysine side‐chain amines or N‐terminal amines on proteins, peptides, and amine‐modified oligonucleotides under mild conditions (pH 7–9). The resulting amide bond is stable and physiologically compatible.
Schematic illustrating the NHS ester–amine coupling between an NHS ester‐activated dye and an amine‐modified biomolecule. NHS esters react readily with lysine side‐chain amines or N‐terminal amines on proteins, peptides, and amine‐modified oligonucleotides under mild conditions (pH 7–9). The resulting amide bond is stable and physiologically compatible.
Schematic illustrating the NHS ester–amine coupling between an NHS ester‐activated dye and an amine‐modified biomolecule. NHS esters react readily with lysine side‐chain amines or N‐terminal amines on proteins, peptides, and amine‐modified oligonucleotides under mild conditions (pH 7–9). The resulting amide bond is stable and physiologically compatible.