Flamma® 496 Hydrazide

Product#: CWH1001
$1,100.80

Size of product (mg)

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

Flamma® 496 Hydrazide

Cat. No. List below

Description

Flamma® Fluors 496 Hydrazide is a powerful and versatile fluorescent dye designed for advanced bioimaging applications. This reactive form of bright green dye, derived from the fluorescein structure, offers exceptional stability in fluorescence signaling and is optimized for labeling biomolecules bearing aldehyde or ketone groups.

Key features:
1. Excitation/Emission maxima: 496/520 nm
2. High extinction coefficient: ≥ 43,000 cm?¹M?¹
3. Hydrazide reactive group for specific aldehyde and ketone labeling
4. Yellow solid appearance
5. Molecular weight: 428.34 g/mol
6. Soluble in DMF and DMSO
7. Spectrally similar to Alexa488, FITC, and Cy2

Applications:
1. Labeling of polysaccharides and glycoproteins
2. Visualization of free reducing sugars on biomolecules
3. Bioimaging of aldehyde and ketone-bearing molecules
4. Potential use in flow cytometry and fluorescence microscopy
5. Applicable in studies involving carbohydrate chemistry and glycobiology

Advantages:
1. Generates stable fluorescence signals in bioimaging
2. Excellent optical properties when excited with a 488 nm laser line
3. Forms stable imine linkages through reductive amination reactions
4. Enables labeling of biomolecules after oxidation of primary and secondary alcohols
5. Offers compatibility with common fluorescence instrumentation
6. Provides a bright green fluorescence signal with minimal background

Flamma® Fluors 496 Hydrazide exhibits maximal excitation at 496 nm and emission at 520 nm, placing it in the same spectral range as other popular green fluorescent dyes. This spectral similarity allows for easy integration into existing imaging protocols and systems using standard FITC filter sets.

The hydrazide reactive group of Flamma® 496 is highly selective for aldehyde and ketone groups, forming stable imine linkages through reductive amination reactions. This selectivity makes it particularly useful for labeling free reducing sugars on biomolecules. For applications involving polysaccharides and glycoproteins, researchers can oxidize primary and secondary alcohols to aldehydes and ketones prior to conjugation, expanding the range of targetable molecules.

Engineered to perform in complex biological environments, Flamma® Fluors 496 Hydrazide exhibits excellent solubility in DMF and DMSO. Its bright green fluorescence and high extinction coefficient ensure strong signal generation even at low concentrations, enabling the visualization of low-abundance biological structures with great sensitivity.

The dye's stability and excellent optical properties make it suitable for various advanced bioimaging techniques, including fluorescence microscopy and flow cytometry. Its compatibility with the 488 nm laser line, commonly found in many imaging systems, further enhances its versatility in research settings.

For optimal results and longevity, store Flamma® Fluors 496 Hydrazide at -20°C and protect it from light. With its superior brightness, excellent photostability, and specific reactivity towards aldehydes and ketones, this dye empowers researchers to achieve high-quality imaging results in studies involving carbohydrate chemistry, glycobiology, and related fields.
 
Specifications
  • Fluorophore: Flamma® Fluors 496
  • Reactive group: Hydrazide
  • Excitation/Emission Max.(nm): 496/520 
  • Spectrally similar dyes: Alexa488, FITC, Cy2
  • Extinction coefficient: ≥ 43,000 cm-1M-1
  • CF280: 0.12
  • Appearance: Yellow Solid
  • Molecular Weight: 428.34 g/mol    
  • Solubility: DMF, DMSO
  • Storage conditions: -20 ℃, protect from light
 
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm) Spectrally similar dyes
CWH1001 Flamma® 496 Hydrazide 496 520 Alexa488, FITC, Cy2
PWH1122 Flamma® 552 Hydrazide 550 564 Alexa555, DyLight549, Cy3, ATTO550
KWH1415 Flamma® 581 Hydrazide 578 593 Alexa594, DyLight594
PWH1215 Flamma® 648 Hydrazide 648 663 Alexa647, DyLight650, Cy5
PWH1515 Flamma® 675 Hydrazide 675 691 Alexa680, DyLight680, Cy5.5, IRDye680LT, CF680
PWH1301 Flamma® 749 Hydrazide 749 774 Alexa750, DyLight755, Cy7.5, IRDye750
PWH1603 Flamma® 774 Hydrazide 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 Hydrazide 

 


Flamma® Fluors hydrazide dyes can label aldehyde and ketone through reductive amination reaction to form an imine linkage. The main labeling target for hydrazides are free reducing sugars on biomolecules, and prior to conjugation, primary and secondary alcohols on polysaccharide and glycoprotein are usually oxidized to aldehyde and ketone. Fluorescent modification of aldehyde or carbonyl groups in carbohydrates is also frequently utilized for their analysis by HPLC, capillary electrophoresis and other methods. Hydrazide dyes can also label biomolecules, which introduced aldehyde by genetical or chemical modification.

 

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.

 

logo_Bioacts.png

Satisfaction
Quality Rating
Value Rating
Style Rating
X