Flamma® 648 Azide

Product#: PWZ1215
$1,100.80

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
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Flamma® 648 Azide

Cat. No. List below

Description


Flamma® Fluors 648 Azide is a state-of-the-art far-red fluorescent dye specifically engineered for copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions in bioimaging applications. This innovative reagent combines the power of click chemistry with exceptional fluorescence properties, offering researchers a versatile and efficient tool for advanced cellular imaging and biomolecule labeling.

Key Features and Advantages:
  • Optimal Spectral Properties: Excitation/emission maxima at 648/663 nm, comparable to popular dyes like Alexa 647, Cy5, and DyLight 650.
  • Versatile Excitation: Compatible with 593 or 633 nm laser lines, providing flexibility in imaging setups.
  • Superior Brightness: High extinction coefficient of ≥ 227,000 cm-1M-1 ensures vivid fluorescence signals.
  • Minimal Protein Interference: Low CF280 value of 0.023 reduces interference with protein absorbance measurements.
  • Strategic Azide Positioning: Azide group connected via an amino propyl linkage for optimal reactivity.
  • Bioorthogonal Labeling: Forms 1,4-disubstituted 1,2,3-triazoles without disrupting native biochemical processes.
Flamma® Fluors 648 Azide excels in various applications, including advanced cellular imaging (ideal for high-resolution live-cell and fixed-cell microscopy), nucleotide functionalization (enables specific labeling of alkyne-modified nucleic acids), protein labeling (excellent for tracking alkyne-modified proteins in complex biological systems) and biomolecule tracking (suitable for studying dynamics of various alkyne-tagged biomolecules in living systems). 

The Click Chemistry Advantage: 
The azide reactive group allows for highly specific and efficient labeling through CuAAC reactions:
  • Bioorthogonal: Reactions occur without interfering with native biological processes.
  • High Specificity: Selective labeling of alkyne-modified biomolecules.
  • Versatility: Compatible with a wide range of alkyne-functionalized targets.
  • Mild Reaction Conditions: Suitable for various biological systems and pH ranges.
For best results. introduce alkyne functionality to target biomolecules via chemical or genetic modification, perform CuAAC reaction under optimized conditions (e.g., copper catalyst, reducing agent, ligand), purify labeled biomolecules using standard chromatographic techniques, and verify labeling efficiency through spectrophotometric analysis.
 
Specifications
  • Fluorophore: Flamma® Fluors 648
  • Reactive group: Azide
  • Excitation/Emission Max.(nm): 648/663 
  • Spectrally similar dyes: Alexa647, DyLight650, Cy5
  • Extinction coefficient: ≥ 227,000 cm-1M-1
  • CF280: 0.023
  • Appearance: Blue Solid
  • Molecular Weight: 766.97 g/mol    
  • Solubility: DMF, DMSO
  • Storage conditions: -20 ℃, protect from light
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
CWZ1001 Flamma® 496 Azide 496 520 Alexa488, FITC, Cy2
PWZ1122 Flamma® 552 Azide 550 564 Alexa555, DyLight549, Cy3, ATTO550
KWZ1415 Flamma® 581 Azide 581 596 Alexa594, DyLight594
PWZ1215 Flamma® 648 Azide 648 663 Alexa647, DyLight650, Cy5
PWZ1515 Flamma® 675 Azide 674 691 Alexa680, DyLight680, Cy5.5, IRDye680LT
PWZ1301 Flamma® 749 Azide 749 774 Alexa750, DyLight755, Cy7.5, IRDye750
PWZ1603 Flamma® 774 Azide 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
Why Choose Flamma® Fluors 648 Azide?
  • Cutting-Edge Technology: Combines click chemistry with far-red fluorescence for advanced bioimaging.
  • Exceptional Brightness: High extinction coefficient for clear, vivid signals even at low concentrations.
  • Versatility: Suitable for various alkyne-modified biomolecules and imaging techniques.
  • Minimal Background: Low CF280 value ensures high signal-to-noise ratio in protein studies.
  • Optimized Design: Amino propyl linkage provides ideal spacing for efficient click reactions.
 

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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