Flamma® 675 ADIBO

Product#: DWC1051
$1,100.80

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
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Flamma® 675 ADIBO

Cat. No. List below

Description

Flamma® Fluors 675 ADIBO is an advanced near-infrared (NIR) fluorescent dye designed for cutting-edge bioimaging applications. This strain-promoted azide-alkyne cycloaddition (SPAAC) reagent is derived from a benzindocyanine structure, offering a stable and robust fluorescence signal ideal for various biological imaging techniques.

Spectral Properties:
Excitation/Emission maxima: 674/688 nm
Spectrally similar to Alexa 680, Cy5.5, IRDye 680LT, and DyLight 680
Can be excited using a 633 nm laser line
Emits in the NIR region, allowing for deep tissue penetration
Chemical Reactivity

Flamma 675 ADIBO is engineered for copper-free click chemistry reactions. It couples with azide-functionalized biomolecules to form 1,4-disubstituted 1,2,3-triazoles through SPAAC reactions. This process occurs efficiently in living systems without the need for coupling reagents or catalysts, preserving native biochemical processes.

Its applications are cellular imaging, nucleotide functionalization, in vivo and in vitro bioimaging, and bioorthogonal labeling in complex biological environments.

To utilize Flamma 675 ADIBO, introduce azide functionality to the target biomolecule through chemical or genetic modification. Then perform the SPAAC reaction to couple the dye with the azide-modified target. Finally, proceed with imaging or further experimental procedures

The NIR emission of Flamma 675 ADIBO makes it particularly valuable for in vivo imaging applications. NIR light can penetrate deeper into biological tissues compared to visible light, allowing for enhanced signal-to-noise ratios and improved imaging depth. 

The ADIBO reactive group's strain-promoted cycloaddition chemistry allows for rapid and efficient labeling under mild conditions, It is ideal for sensitive biological samples and live-cell imaging
Potential for multiplexing with other fluorophores due to its distinct spectral properties

Flamma® Fluors 675 ADIBO represents a state-of-the-art tool in modern biomedical research, offering high sensitivity, specificity, and versatility for a wide range of imaging and labeling applications, particularly where copper-free click chemistry is desired or required.

 
Specifications
  • Fluorophore: Flamma® Fluors 675
  • Reactive group: ADIBO
  • Excitation/Emission Max.(nm): 674/688 
  • Spectrally similar dyes: Alexa680, DyLight680, Cy5.5, IRDye680LT
  • Extinction coefficient: ≥ 220,000 cm-1M-1
  • Appearance: Blue Solid
  • Molecular Weight: 1203.42 g/mol    
  • Solubility: DMF, DMSO
  • Storage conditions: -20 ℃, protect from light  
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
DWC1001 Flamma® 496 ADIBO 496 520 Alexa488, FITC, Cy2
DWC1011 Flamma® 552 ADIBO 550 564 Alexa555, DyLight549, Cy3, ATTO550
DWC1415 Flamma® 581 ADIBO 581 596 Alexa594, DyLight594
DWC1021 Flamma® 648 ADIBO 648 663 Alexa647, DyLight650, Cy5
DWC1051 Flamma® 675 ADIBO 674 691 Alexa680, DyLight680, Cy5.5, IRDye680LT
DWC1031 Flamma® 749 ADIBO 749 774 Alexa750, DyLight755, Cy7.5, IRDye750
DWC1061 Flamma® 774 ADIBO 774 800 Cy7.5, DyLight800, IRDye800


Background

Flamma® Fluors

BioActs offers a broad range of Flamma® Fluors dyes equipped with variety of reactive and functional groups, which can cover the full spectral range from UV to NIR with their excellent fluorescence performance. Characteristic features of these superior dyes are strong absorption, high fluorescence quantum yield and high photostability. Flamma® dyes maintain good fluorescence activity and stability after conjugation to biomolecules and allow the detection of low-abundance biological structures with great sensitivity. The dyes are compatible with optical conditions of most of fluorescent equipment and are ideal for any applications in biological studies.
  • Covering the full spectral range from UV to NIR
  • Equipped with a variety of reactive groups: NHS and Sulfo-NHS ester, Vinylsulfone, Maleimide, Click chemistry, isothiocyanate, hydrazide and hydrophobic substances.
  • High quantum yields and photostability
  • High purity and compatible with most of biomolecules
Advantages of SPAAC:
  • Copper-free: Eliminates potential toxicity associated with copper catalysts
  • Fast reaction kinetics: ADIBO's strained alkyne structure promotes rapid cycloaddition
  • Biocompatible: Efficient under physiological conditions
  • Clean reaction: Produces no interfering by-products
 

Flamma® Fluors for Click Chemistry

The most widely utilized click chemistry is 1,3-dipolar cycloaddition between an azide and an alkyne to produce 1,4-disubstituted 1,2,3-triazole. There are two types of 1,3-dipolar cycloaddition methods: copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC). BioActs offers Flamma® Fluors Alkyne dyes for CuAAC, Flamma® Fluors ADIBO products for SPAAC and Flamma® Fluors Azide dyes for both CuAAC and SPAAC.

  

Figure 1.   Absorption (upper) and emission (bottom) spectra overlap of Flamma® Fluors

 

Figure 2.   Immunofluorescence imaging and in situ hybridization imaging

 

Figure 3.   Fluorescence images of Flamma® 749 (upper) and Flamma® 774 (bottom) carboxylic acid injected mouse model


Citation & Reference

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4. Yhee, Ji Young. Tumor-targeting transferrin nanoparticles for systemic polymerized siRNA delivery in tumor-bearing mice. Bioconjugate chemistry 24.11 (2013): 1850-1860.
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6. Ryu, Ju Hee. Early diagnosis of arthritis in mice with collagen?induced arthritis, using a fluorogenic matrix metalloproteinase 3–specific polymeric probe. Arthritis & Rheumatism 63.12 (2011): 3824-3832.
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9. Zhu, Lei. Real-time monitoring of caspase cascade activation in living cells. Journal of controlled release 163.1 (2012): 55-62.
10. Yoon, Hong Yeol. Bioreducible hyaluronic acid conjugates as siRNA carrier for tumor targeting. Journal of Controlled Release 172.3 (2013): 653-661.
11. Yhee, Ji Young. Cancer-targeted MDR-1 siRNA delivery using self-cross-linked glycol chitosan nanoparticles to overcome drug resistance. Journal of Controlled Release 198 (2015): 1-9.
12. Park, Jin Woo. Wide-Ranged Fluorescent Molecular Weight Size Markers for Electrophoresis. Bulletin of the Korean Chemical Society 34.1 (2013): 29-30.
13. Huang, Xinglu. Multiplex Imaging of an Intracellular Proteolytic Cascade by using a Broad?Spectrum Nanoquencher. Angewandte Chemie International Edition 51.7 (2012): 1625-1630.

 

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