Flamma® 749 Amine

Product#: PWE1301
$1,100.80

Size of product (mg)

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

Cat. No. List below

Description

Flamma® Fluors 749 Amine is an advanced near-infrared (NIR) fluorescent dye derived from a cyanine structure, engineered for cutting-edge bioimaging applications. This versatile fluorophore offers exceptional stability and optical properties for generating reliable fluorescence signals in complex biological environments.

Key features:
1. Excitation/Emission maxima: 749/774 nm
2. Primary amine functional group attached through a spacer
3. Spectral similarity to popular NIR dyes (Alexa 750, Cy7, IRDye 750, DyLight 755)
4. Soluble in DMF and DMSO

Applications:
1. Bioimaging and fluorescence microscopy
2. In vitro and in vivo imaging studies
3. Coupling with carboxylic acids on small molecules or biomolecules
4. Reference standard for dye-conjugates
5. Deep-tissue and whole-body imaging
6. Potential use in fluorescence-guided surgery
7. Protein labeling and antibody conjugation
8. Nucleic acid tagging
9. Nanoparticle functionalization

Advantages:
1. Enhanced tissue penetration due to NIR spectral properties
2. Reduced autofluorescence and light scattering in biological samples
3. Compatibility with 750 nm laser line or dye-pumped laser excitation
4. Versatile coupling options through standard amide bond formation
5. Stable fluorescence signal for extended imaging sessions
6. High sensitivity for detecting low-abundance biological structures
7. Potential for multiplexing with other fluorophores in different spectral regions
8. Reduced phototoxicity for biological components

 
 
Specifications
  • Fluorophore: Flamma® Fluors 749
  • Functional group: Primary amine
  • Excitation/Emission Max.(nm): 749/774 
  • Spectrally similar dyes: Alexa750, DyLight755, Cy7, IRDye750
  • Extinction coefficient: ≥ 200,000 cm-1M-1
  • CF280: 0.03
  • Appearance: Green Solid
  • Molecular Weight: 752.98 g/mol
  • Solubility: DMF, DMSO
  • Storage conditions: 4 ℃, protect from light 
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
CWE1001 Flamma® 496 Amine 496 520 Alexa488, FITC, Cy2
PWE1122 Flamma® 552 Amine 550 565 Alexa555, DyLight549, Cy3, ATTO550
KWE1415 Flamma® 581 Amine 578 593 Alexa594, DyLight594
PWE1215 Flamma® 648 Amine 648 663 Alexa647, DyLight650, Cy5
PWE1515 Flamma® 675 Amine 675 691 Alexa680, DyLight680, Cy5.5, IRDye680LT, CF680
PWE1301 Flamma® 749 Amine 749 774 Alexa750, DyLight755, Cy7.5, IRDye750
PWE1603 Flamma® 774 Amine 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 749 Amine Advantages:
1. Reduced photobleaching compared to visible light fluorophores
2. Lower background fluorescence in biological samples
3. Potential for multiplexing with other fluorophores in different spectral regions
These properties make Flamma® Fluors 749 Amine a valuable tool for researchers in fields such as molecular biology, biochemistry, and biomedical imaging, where high-sensitivity detection and low background interference are crucial.

Flamma® Fluors Amine

Flamma® Fluors Amine dyes have an attached primary amine, which connected through a spacer, and can be used as a reference standard for dye-conjugates. These amine dyes can be conjugated with carboxylic acids at small molecules or peptides by standard amide bond coupling conditions.

 

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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