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AAT Bioquest

XFD700 alkyne

Product key features

  • Ex/Em: 696/719 nm
  • Extinction coefficient: 192,000 cm-1M-1
  • Reactive Group: Alkyne
  • Efficient Conjugation: Click chemistry labeling of azides on peptides, antibodies, and other biomolecules
  • Moderate Brightness: Suitable for high-abundance targets, preserving brighter dyes for low-abundance detection.
  • Water Soluble: Minimizes aggregation, enhancing signal clarity for advanced imaging and live-cell studies
  • Panel Optimization: Enhances spectral resolution between APC and APC-iFluor® 780 in multicolor assays.

Product description

XFD700, manufactured by AAT Bioquest, is a near-infrared fluorescent dye structurally identical to Alexa Fluor™ 700 (ThermoFisher). It is optimally excited by 633–640 nm laser lines and offers a relatively low fluorescence intensity, making it particularly well-suited for direct imaging of high-abundance targets in both microscopy and flow cytometry. This allows researchers to allocate brighter dyes for detecting lower-abundance antigens, improving overall panel design. XFD700 exhibits excellent aqueous solubility and maintains consistent fluorescence stability across a broad pH range (pH 4–10), ensuring robust and reproducible performance under diverse experimental conditions. Its long-wavelength emission effectively minimizes background autofluorescence, leading to enhanced signal-to-noise ratios, especially in complex biological samples such as tissues. In multicolor flow cytometry panels, XFD700 serves as an ideal option between APC and APC-iFluor® 780, enabling better resolution in complex assays.

The alkyne derivative of XFD700 is widely used for labeling azides on peptides, antibodies, and other biomolecules via click chemistry. It participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with azide-containing molecules.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
XFD488 alkyne *Same Structure to Alexa Fluor™ 488 alkyne*499520710000.9210.300.11
XFD555 alkyne5535681500000.110.080.08
XFD635 alkyne633647140,000---
XFD647 Alkyne6506712700000.331-0.03
XFD680 alkyne6817041840000.3610.000.05
XFD700 TCO6967191920000.2510.000.07
XFD700 Tetrazine6967191920000.2510.000.07
XFD750 alkyne7527762400000.1210.000.04
XFD790 alkyne782805260,000-0.090.08
Page updated on April 15, 2025

Ordering information

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Unit size
Catalog Number70115
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Additional ordering information

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Physical properties

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.00

Correction Factor (280 nm)

0.07

Extinction coefficient (cm -1 M -1)

192000

Excitation (nm)

696

Emission (nm)

719

Quantum yield

0.251

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 azide–alkyne cycloaddition (“click chemistry”) between an alkyne‐functionalized dye and an azide‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions, tolerates a wide range of functional groups, and is frequently used to label proteins, nucleic acids, and other biomolecules for imaging, proteomics, and high‐throughput assays.
Schematic illustrating the azide–alkyne cycloaddition (“click chemistry”) between an alkyne‐functionalized dye and an azide‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions, tolerates a wide range of functional groups, and is frequently used to label proteins, nucleic acids, and other biomolecules for imaging, proteomics, and high‐throughput assays.
Schematic illustrating the azide–alkyne cycloaddition (“click chemistry”) between an alkyne‐functionalized dye and an azide‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions, tolerates a wide range of functional groups, and is frequently used to label proteins, nucleic acids, and other biomolecules for imaging, proteomics, and high‐throughput assays.