Flamma® 675 Maleimide

Product#: PWM1415
$1,100.80

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
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Flamma® 675 Maleimide

Cat. No. List below

Description

Flamma® Fluors 675 Maleimide is a cutting-edge near-infrared (NIR) fluorescent dye engineered for advanced bioimaging applications. This thiol-reactive fluorophore, derived from a benzindocyanine structure, offers exceptional stability in fluorescence signaling, making it an invaluable tool for researchers in life sciences.

Key features:
1. Excitation/Emission maxima: 675/691 nm
2. High extinction coefficient: ≥ 200,000 cm?¹M?¹
3. Maleimide reactive group for specific thiol labeling
4. Blue solid appearance
5. Molecular weight: 1067.23 g/mol
6. Soluble in DMF and DMSO

Applications:
1. Protein labeling (antibodies, peptides, proteins)
2. Ligand labeling for receptor studies
3. Amplification substrates in signal amplification techniques
4. In vitro imaging with high-sensitivity detection in fixed cells
5. Deep-tissue ex vivo and in vivo imaging
6. Potential use in super-resolution microscopy and single-molecule detection
7. Fluorescence lifetime imaging (FLIM) studies

Advantages:
1. Exceptional stability in fluorescence signaling
2. Optimal NIR spectrum operation, minimizing autofluorescence and allowing deep tissue penetration
3. Spectral similarity to popular NIR dyes (Alexa 680, Cy5.5, IRDye 680LT, DyLight 680, CF680)
4. Efficient excitation using a 633 nm laser line
5. Highly selective labeling of thiol groups, particularly cysteine residues
6. Formation of stable thioether linkages
7. Excellent performance in complex biological environments
8. Potential for multi-color imaging experiments
9. Reduced phototoxicity due to longer excitation wavelengths

Flamma® Fluors 675 Maleimide operates in the optimal NIR spectrum, with excitation at 675 nm and emission at 691 nm. This spectral range minimizes autofluorescence from biological samples, reduces light scattering, and allows for deep tissue penetration, making it ideal for in vivo and ex vivo imaging studies. The dye's high extinction coefficient (≥ 200,000 cm?¹M?¹) ensures brilliant fluorescence intensity, enabling the visualization of low-abundance biomolecules with exceptional clarity.

The maleimide reactive group enables highly specific and efficient labeling of thiol groups in biomolecules, particularly cysteine residues, via a 1,4-addition pathway. This selectivity results in minimal off-target labeling, producing cleaner and more accurate imaging results. The formed thioether linkages are exceptionally stable, providing long-lasting fluorescence signals ideal for extended imaging sessions. However, researchers should note that under strongly basic conditions, the dye may also react with primary amines.

Engineered to perform in complex biological environments, Flamma® Fluors 675 Maleimide exhibits excellent solubility in DMF and DMSO. Its spectral similarity to widely-used NIR dyes allows for seamless integration into existing imaging protocols and systems, making it a versatile choice for various advanced bioimaging techniques.

The NIR properties of Flamma® 675 Maleimide make it particularly valuable for in vivo imaging applications, enabling deeper penetration and reduced scattering in biological tissues. This characteristic is especially beneficial for studying complex biological systems, such as small animal models. Additionally, the dye's potential compatibility with fluorescence lifetime imaging (FLIM) techniques opens up possibilities for quantitative functional imaging studies.

For optimal results and longevity, store Flamma® Fluors 675 Maleimide at -20°C and protect it from light. With its superior brightness, excellent photostability, and high specificity, this dye empowers researchers to achieve unprecedented clarity and precision in their cellular and molecular imaging studies, contributing significantly to our understanding of complex biological processes at the molecular level.
 
Specifications
  • Fluorophore: Flamma® Fluors 675
  • Reactive group: Maleimide
  • Excitation/Emission Max.(nm): 675/691 
  • Spectrally similar dyes: Alexa680, DyLight680, Cy5.5, IRDye680LT, CF680
  • Extinction coefficient: ≥ 200,000 cm-1M-1
  • CF280: 0.18
  • Appearance: Blue Solid
  • Molecular Weight: 1067.23 g/mol   
  • Solubility: DMF, DMSO
  • Storage conditions: -20 ℃, protect from light 
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
CWM1001 Flamma® 496 Maleimide 496 520 Alexa488, FAM
CWM1058 Flamma® 552 Maleimide 550 565 Alexa555, DyLight549, Cy3, ATTO550, CF555
KWM1415 Flamma® 581 Maleimide 581 596 Alexa594, DyLight594
KWM1042 Flamma® 648 Maleimide 648 663 Alexa647, DyLight650, Cy5, ATTO 647N, CF647
PWM1415 Flamma® 675 Maleimide 675 691 Alexa680, DyLight680, Cy5.5, IRDye680LT, CF680
PWM1215 Flamma® 749 Maleimide 749 774 Alexa750, DyLight755, Cy7, IRDye750
PWM1515 Flamma® 774 Maleimide 774 806 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
What are the advantages?
  • High Sensitivity: Capable of detecting low-abundance biomolecules in fixed cells.
  • NIR Emission: Allows for deep tissue penetration in biological samples.
  • Stability: Provides consistent and reliable fluorescence signals.
  • Versatility: Compatible with a wide range of biomolecules and imaging techniques.
 

Flamma® Fluors maleimide

Maleimide is an excellent reactive group that can specially label thiol of cysteine residue without interacting with amino functionality. In labeling process, thiol is added to the double bond of maleimide via 1,4-addition pathway to form thioether linkage. Maleimides apparently do not react with methionine, histidine or tyrosine, but they are reacted with amines in higher pH than reaction of maleimides. BioActs offers Flamma® Fluors maleimide series as thiol-reactive fluorescence dyes.

 
 

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

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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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