Flamma® 552 Maleimide

Product#: CWM1058
$1,100.80

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
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Flamma® 552 Maleimide

Cat. No. List below

Description

Flamma® Fluors 552 Maleimide is a versatile and highly effective thiol-reactive fluorescent dye designed for advanced bioimaging applications. This bright yellow dye generates stable fluorescence signals, making it ideal for sensitive detection and labeling of various biomolecules.

Key Features
1. High sensitivity for detecting low-abundance biomolecules
2. Excellent optical properties and photostability
3. Selective labeling of thiol groups on cysteine residues
4. Forms stable thioether linkages
5. Compatible with various biomolecules and cellular structures

Applications
1. Labeling of thiols on antibodies, peptides, proteins, and ligands
2. Cellular labeling and detection
3. Fluorescence microscopy
4. Flow cytometry
5. Multicolor imaging (compatible with other fluorophores)
6. Amplification substrate labeling

Advantages
1. High fluorescence quantum yield for bright signals
2. Minimal interaction with other amino acids (methionine, histidine, tyrosine)
3. Versatile for use in various biological studies
4. Maintains good fluorescence activity and stability after conjugation
5. Allows detection of low-abundance biological structures
6. Compatible with most fluorescent equipment

Flamma® Fluors 552 Maleimide offers researchers a powerful tool for precise and sensitive labeling in a wide range of biological applications. Its excellent spectral properties, high photostability, and specific reactivity make it an ideal choice for advanced fluorescence-based studies and imaging techniques.
 
Specifications
  • Fluorophore: Flamma® Fluors 552
  • Reactive group: Maleimide
  • Excitation/Emission Max.(nm): 550/565 
  • Spectrally similar dyes: Alexa555, DyLight549, Cy3, ATTO550, CF555
  • Extinction coefficient: ≥ 136,000 cm-1M-1
  • CF280: 0.07
  • Appearance: Red Solid
  • Molecular Weight: 793.3 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
 

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

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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