Flamma® 648 Alkyne

Product#: PWK1215
$1,336.00

Size of product (mg)

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

Cat. No. List below

Description


Flamma® Fluors 648 Alkyne is a state-of-the-art far-red fluorescent dye specifically designed 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 tool for cellular imaging and biomolecule labeling.

Key Features and Benefits:
  • 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 0.024 reduces interference with protein absorbance measurements.
  • Bioorthogonal Labeling: Forms 1,4-disubstituted 1,2,3-triazoles without disrupting native biochemical processes.
Flamma® Fluors 648 Alkyne excels in various applications, including cellular imaging (ideal for live-cell and fixed-cell microscopy), nucleotide functionalization (enables specific labeling of modified nucleic acids), protein labeling (excellent for tracking proteins in complex biological systems), and biomolecule tracking (suitable for studying dynamics of various biomolecules in living systems).

Its chemistry advantage is the alkyne reactive group allows for highly specific and efficient labeling through CuAAC reactions, which are bioorthogonal (reactions occur without interfering with native biological processes), has high specificity (selective labeling of azide-modified biomolecules) and has mild reaction conditions (compatible with a wide range of biological systems).

For best results, introduce azide functionality to target biomolecules via chemical or genetic modification. Perform CuAAC reaction under optimized conditions (e.g., copper catalyst, reducing agent) and purify labeled biomolecules using standard chromatographic techniques.


 
Specifications
  • Fluorophore: Flamma® Fluors 648
  • Reactive group: Alkyne
  • Excitation/Emission Max.(nm): 648/663 
  • Spectrally similar dyes: Alexa647, DyLight650, Cy5
  • Extinction coefficient: ≥ 227,000 cm-1M-1
  • CF280: 0.024
  • Appearance: Blue Solid
  • Molecular Weight: 721.93 g/mol       
  • Solubility: DMF, DMSO
  • Storage conditions: -20 ℃, protect from light
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
CWK1001 Flamma® 496 Alkyne 496 520 Alexa488, FITC, Cy2
PWK1122 Flamma® 552 Alkyne 550 564 Alexa555, DyLight549, Cy3, ATTO550
KWK1415 Flamma® 581 Alkyne 581 596 Alexa594, DyLight594
PWK1215 Flamma® 648 Alkyne 648 663 Alexa647, DyLight650, Cy5
PWK1515 Flamma® 675 Alkyne 674 691 Alexa680, DyLight680, Cy5.5, IRDye680LT
PWK1301 Flamma® 749 Alkyne 749 774 Alexa750, DyLight755, Cy7.5, IRDye750
PWK1603 Flamma® 774 Alkyne 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 Alkyne?
  • Cutting-Edge Technology: Combines click chemistry with far-red fluorescence for advanced bioimaging.
  • Exceptional Brightness: High extinction coefficient for clear, vivid signals.
  • Versatility: Suitable for various biomolecules and imaging techniques.
  • Minimal Background: Low CF280 value ensures high signal-to-noise ratio.
 

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.
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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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