Flamma® 552 Carboxylic acid

Product#: PWC1101
$778.24

Size of product (mg)

  • 1 mg
  • 5 mg
  • 25 mg
Availability:
Ships in 1-2 Weeks

Flamma® 552 Carboxylic acid

Cat. No. List below

Description

Flamma® Fluors 552 Carboxylic acid is an advanced fluorescent dye designed for versatile applications in bioimaging. This bright yellow fluorophore, derived from a cyanine structure, offers exceptional stability and optical properties for generating reliable fluorescence signals.

Key features:
1. Excitation/Emission maxima: 550/565 nm
2. High extinction coefficient: ≥ 150,000 cm?¹M?¹
3. Low CF280: 0.07
4. Carboxylic acid functional group
5. Red solid appearance
6. Molecular weight: 672.85 g/mol
7. Soluble in DMF and DMSO

Applications:
1. Bioimaging and fluorescence microscopy
2. Reference standard for dye-conjugates
3. Coupling with primary amines on small molecules or biomolecules
4. Potential use in flow cytometry and fluorescence-based assays
5. Cellular labeling and detection

Advantages:
1. Spectral similarity to popular dyes (Alexa 555, DyLight 549, ATTO 550, Cy3)
2. Excellent optical properties when excited with 532, 543, 546, or 555 nm laser lines
3. Versatile coupling options through standard amide bond formation
4. Potential for conversion to reactive amine form
5. Stable fluorescence signal for extended imaging sessions
 
Specifications
  • Fluorophore: Flamma® Fluors 552
  • Functional group: Carboxylic acid
  • Excitation/Emission Max.(nm): 550/565  
  • Spectrally similar dyes: Alexa555, DyLight549, Cy3, ATTO550
  • Extinction coefficient: ≥ 150,000 cm-1M-1
  • CF280: 0.07
  • Appearance: Red Solid
  • Molecular Weight: 672.85 g/mol    
  • Solubility: DMF, DMSO
  • Storage conditions: 4 ℃, protect from light
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
PWC1101 Flamma® 552 Carboxylic acid 550 565 Alexa555, DyLight549, Cy3, ATTO550
PWC1201 Flamma® 648 Carboxylic acid 648 663 Alexa647, DyLight650, Cy5
PWC1501 Flamma® 675 Carboxylic acid 675 691 Alexa680, DyLight680, Cy5.5, IRDye680LT, CF680
PWC1308 Flamma® 749 Carboxylic acid 749 774 Alexa750, DyLight755, Cy7, IRDye750
PWC1603 Flamma® 774 Carboxylic acid 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 Carboxylic acid 

 


Flamma® Fluors Carboxylic acids are non-reactive form of Flamma® Fluors that can be used as a reference standard for dye-conjugates. Additionally, this carboxylic acid can be converted to a reactive amine form by using standard chemical techniques or coupled to hydrazines. Flamma® Fluors carboxylic acids can be coupled with amines 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.
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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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