Flamma® 749 ADIBO

Product#: DWC1031
$1,100.80

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
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Flamma® 749 ADIBO

Cat. No. List below

Description

Flamma® Fluors 749 ADIBO is a specialized near-infrared (NIR) fluorescent dye designed for strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, enabling stable fluorescence signals in bioimaging applications. This innovative dye is derived from a cyanine structure and features an alkyne reactive group connected to the dye through an ADIBO (1,8-diamino-3,6-dioxaoctane) spacer, enhancing its solubility and biocompatibility.

The dye exhibits excitation and emission maxima at 749 nm and 774 nm, respectively, which places it in the NIR region of the spectrum. These spectral characteristics are similar to other well-known NIR dyes such as Alexa 750, Cy7, IRDye 750, and DyLight 755. Flamma 749 can be efficiently excited using a 750 nm laser line or dye-pumped laser, with emission occurring in the NIR region, making it particularly advantageous for biological tissue imaging due to improved penetration and reduced autofluorescence.

Flamma® Fluors 749 ADIBO participates in SPAAC reactions, coupling with azide-functionalized biomolecules to form 1,4-disubstituted 1,2,3-triazoles without the need for coupling reagents or catalysts. This unique feature allows for efficient labeling inside living systems while preserving native biochemical processes. To utilize this dye effectively, researchers must first introduce azide functionality onto the target biomolecule through chemical or genetic modification.

Flamma® Fluors 749 ADIBO is particularly useful for cellular imaging (provides stable fluorescence signals for various biological imaging applications), nucleotide functionalization (enables specific labeling of nucleic acids), bioconjugation (facilitates the attachment of the dye to various biomolecules through click chemistry), and in vivo imaging (the NIR properties make it suitable for deep tissue imaging without interfering with biological systems).

Flamma® Fluors 749 ADIBO advantages:
1. Reduced Background Fluorescence: The NIR properties minimize interference from biological samples.
2. Enhanced Tissue Penetration: Suitable for in vivo applications where deep tissue imaging is required.
3. Versatile Labeling Options: Can be used for a broad range of biomolecules once azide groups are introduced.

These features make Flamma® Fluors 749 ADIBO a valuable tool for researchers in molecular biology, biochemistry, and biomedical imaging. Its unique reactivity and spectral properties expand the toolkit available for bioconjugation and probe development, particularly in studying complex biological systems within living organisms.

 
Specifications
  • Fluorophore: Flamma® Fluors 749
  • Reactive group: ADIBO
  • Excitation/Emission Max.(nm): 749/774 
  • Spectrally similar dyes: Alexa750, DyLight755, Cy7, IRDye750
  • Extinction coefficient: ≥ 145,000 cm-1M-1
  • Appearance: Green Solid
  • Molecular Weight: 969 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
 

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

1. Xu, Peisheng. Zwitterionic chitosan derivatives for pH-sensitive stealth coating. Biomacromolecules 11.9 (2010): 2352-2358.
2. Ibrahim, Basma M. A strategy to deliver genes to cystic fibrosis lungs: a battle with environment. Journal of controlled release 155.2 (2011): 289-295.
3. Oh, Keun Sang. Accurate sequential detection of primary tumor and metastatic lymphatics using a temperature-induced phase transition nanoparticulate system. International journal of nanomedicine 9 (2014): 2955.
4. Yhee, Ji Young. Tumor-targeting transferrin nanoparticles for systemic polymerized siRNA delivery in tumor-bearing mice. Bioconjugate chemistry 24.11 (2013): 1850-1860.
5. Yoon, Hong Yeol. Glycol chitosan nanoparticles as specialized cancer therapeutic vehicles: Sequential delivery of doxorubicin and Bcl-2 siRNA. Scientific reports 4 (2014).
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.
7. Hollis, Christin P. In vivo investigation of hybrid paclitaxel nanocrystals with dual fluorescent probes for cancer theranostics. Pharmaceutical research 31.6 (2014): 1450-1459.
8. Koo, Heebeom. The movement of self-assembled amphiphilic polymeric nanoparticles in the vitreous and retina after intravitreal injection. Biomaterials 33.12 (2012): 3485-3493.
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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