Flamma® 581 Isothiocyanate

Product#: PWI1415
$8,118.72

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  • 1 mg
  • 5 mg
  • 25 mg
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Flamma® 581 Isothiocyanate

Cat. No. List below

Description

Flamma® Fluors 581 Isothiocyanate is a cutting-edge, reactive orange fluorescent dye derived from a benzindocyanine structure, designed to generate stable fluorescence signals in bioimaging applications. This innovative dye offers exceptional performance and versatility in a wide range of research settings.

Key Features
1. Excitation/Emission maxima at 578/593 nm
2. Compatible with 561, 568, or 578 nm laser lines
3. High extinction coefficient of ≥ 109,000 cm?¹M?¹
4. Excellent optical properties and brightness
5. Moderate reactivity with high stability in water and most organic solvents
6. Forms stable thiourea linkages with primary amines
7. Optimal conjugation at pH above 9

Applications
1. Antibody labeling
2. Peptide and protein tagging
3. Ligand labeling
4. Amplification substrate optimization
5. Cellular labeling and detection
6. Fluorescence microscopy
7. Flow cytometry
8. In vivo imaging
9. Single-molecule detection
10. High-content screening

Advantages
1. Spectral similarity to popular dyes (Alexa594, DyLight594) allows easy integration into existing protocols
2. Superior brightness and photostability compared to traditional fluorophores
3. Versatile conjugation to various biomolecules
4. Stable in challenging experimental conditions
5. Low CF280 value (0.18) minimizes interference with protein absorbance measurements
6. Excellent solubility in DMF and DMSO for flexible experimental design
7. More stable than NHS esters, leading to longer shelf life
8. Suitable for labeling basic-environment tolerable biomolecules

Flamma® Fluors 581 Isothiocyanate is part of the broader Flamma® Fluors series, which covers a full spectral range from UV to NIR. These dyes are characterized by strong absorption, high fluorescence quantum yield, and excellent photostability. They maintain good fluorescence activity and stability after conjugation to biomolecules, allowing for the detection of low-abundance biological structures with great sensitivity.

The isothiocyanate reactive group offers unique advantages for protein modification. While NHS esters typically require a pH of 8.3 for protein labeling, Flamma® 581 Isothiocyanate performs optimally at pH above 9. This higher pH requirement makes it particularly suitable for labeling basic-environment tolerant biomolecules such as DNA and most polysaccharides.

Researchers can leverage Flamma® 581 Isothiocyanate for a wide range of applications in life sciences and biotechnology. Its superior optical properties, stability, and versatility make it a valuable tool for cutting-edge biological studies, drug discovery, and medical diagnostics. The dye's compatibility with various laser lines and fluorescence imaging systems ensures its utility across different experimental setups and instrumentation.
 
Specifications
  • Fluorophore: Flamma® Fluors 581
  • Reactive group: Isothiocyanate
  • Excitation/Emission Max.(nm): 578/593 
  • Spectrally similar dyes: Alexa594, DyLight594
  • Extinction coefficient: ≥ 109,000 cm-1M-1
  • CF280: 0.18
  • Appearance: Purple Solid
  • Molecular Weight: 1003.21 g/mol   
  • Solubility: DMF, DMSO
  • Storage conditions: -20 ℃, protect from light
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
PWI1001 Flamma® 496 Isothiocyanate 494 520 Alexa488, FITC, Cy2
PWI1122 Flamma® 552 Isothiocyanate 550 564 Alexa555, DyLight549, Cy3, ATTO550
PWI1415 Flamma® 581 Isothiocyanate 578 593 Alexa594, DyLight594
KWI1215 Flamma® 648 Isothiocyanate 648 663 Alexa647, DyLight650, Cy5
KWI1515 Flamma® 675 Isothiocyanate 675 691 Alexa680, DyLight680, Cy5.5, IRDye680LT
PWI1308 Flamma® 749 Isothiocyanate 749 774 Alexa750, DyLight755, Cy7.5, IRDye750
PWI1603 Flamma® 774 Isothiocyanate 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 Isothiocyanate

 


BioActs offers a series of Flamma® Fluors isothiocyanates, which are moderately reactive but quite stable in water and most organic solvents. Isothiocyanates form reasonably stable thiourea linkage upon reaction with amines. Whereas labeling of protein with NHS esters can typically be done at pH 8.3, conjugation for isothiocyanates usually require pH above 9. This basic isothiocyanate labeling condition may be a factor for working with basic-environment tolerable biomolecules that DNA and most polysaccharides can be modified in a relatively basic pH. 
 

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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