FSD Fluor™ 488 NHS ester

Product#: KOSC1002
$3,943.36

Size of product (mg)

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

FSD Fluor™ 488 NHS ester

Cat. No. List below

Description

FSD Fluor™ 488 NHS ester is a cutting-edge, amine-reactive fluorescent dye developed by BioActs, offering superior optical properties for a wide range of biochemical and biological analytical applications. This next-generation bright green dye is designed to outperform spectrally similar fluorophores, making it an ideal choice for researchers seeking high sensitivity and excellent fluorescence intensity in their experiments.

FSD Fluor™ 488 NHS ester readily reacts with amine-modified oligonucleotides, proteins (ε-amino groups of lysine or N-terminus), peptides, antibodies, ligands, and amplification substrates.

It has excellent fluorescence intensity after biomolecule conjugation, ideal for single-molecule detection in fluorescence correlation spectroscopy, optimal for fluorescence polarization measurements, and has high sensitivity for low-abundance biomolecule detection. It forms stable amide bonds with target molecules, ensuring long-lasting labeling.

FSD Fluor™ 488 NHS ester represents a significant advancement in fluorescent labeling technology, offering researchers a powerful tool for exploring biological systems with unprecedented sensitivity and clarity. Its combination of bright fluorescence, high photostability, and versatile reactivity makes it an invaluable asset in modern biomedical research, particularly for applications requiring high sensitivity and resolution.

Unique Advantages:
1. Enhanced Brightness: Outperforms spectrally similar dyes in fluorescence intensity
2. High Molar Ratio Labeling: Allows for sensitive detection of low-abundance targets
3. Versatility: Suitable for a wide range of biomolecules and applications
4. Stability: Resistant to photobleaching, enabling extended imaging sessions
5. Compatibility: Spectral properties similar to widely-used dyes, allowing easy integration into existing protocols
 
Specifications
  • Fluorophore: FSD Fluor™ 488
  • Reactive group: NHS ester
  • Excitation/Emission Max.(nm): 495/519
  • Spectrally similar dyes: Alexa 488, FITC, Cy2, Flamma®496
  • Extinction coefficient: ≥ 64,000 cm-1M-1
  • CF280: 0.11
  • Appearance: Orange Solid
  • Molecular Weight: 633.56 g/mol
  • Solubility: DMF
  • Storage conditions: -20 ℃, protect from light
Quick link (Cat.#) FSD series EXmax (nm) EMmax (nm Spectrally similar dyes
KOSC1002 FSD Fluor™ 488 495 519 Alexa Fluor 488, FAM, Cy2
KOSC1003 FSD Fluor™ 555 554 565 Alexa Fluor 555, DyLight 549, Cy3, ATTO 550
KOSC1001 FSD Fluor™ 594 591 617 Alexa Fluor 594, DyLight 594
KOSC1315 FSD Fluor™ 647 651 667 Alexa Fluor 647, Cy5, ATTO 647N, DyLight 650
KOSC1515 FSD Fluor™ 680 679 696 Alexa Fluor 680, Cy5.5, DyLight 680, IRDye 680
KOSC1702 FSD Fluor™ 750 749 774 Alexa Fluor 750, DyLight 755, Cy7, IRDye 750
POSC1803 FSD Fluor™ 800 774 790 Cy7.5, DyLight 800, IRDye 800


Background

FSD Fluor™

FSD Fluor™ is a new generation of dye series with superb fluorescence intensity and high quantum yield comparing to traditional dyes. The fluorescence intensity after binding to biomolecules such as antibody, nucleotide, and protein maintains still excellent, FSD Fluor™ series is ideal for variety of biochemical and biological analytical applications with a less amount of dye conjugate. FSD Fluor™ series equipped with a variety of reactive groups and covers the full fluorescence spectral range from UV to NIR, hence the series is ideal for any applications in fluorescence spectroscopies and biological studies. With superior fluorophores and the wide spectral range, FSD Fluor™ dyes are suitable for every filter and are designed to meet the requirements for complex detection in the field of life science research.

  • Superior fluorescence intensity than any other spectrally similar dyes
  • Maintaining excellent fluorescence after conjugated to biomolecules, surpassing that of any other spectrally similar fluorophore 
    conjugated biomolecules.
  • Higher quantum yield comparing to traditional dyes
  • Equipped with variety of reactive group
  • Covering the full fluorescence spectral range from visible to NIR

 

Figure 1.   Fluorescence intensity comparison of FSD Fluor™ and other dyes

 

Figure 2.   Fluorescence intensity comparison in varying dye/protein ratio

 

Figure 3.   Immunofluorescence comparison of dye-antibody conjugates and photostability test of fluorescent secondary antibodies

 

 Figure 4.   Biodistribution images of FSD Fluor™ 750 and FSD Fluor™ 800


Citation & Reference
 
1. Lim, Chang-Keun. Phthalocyanine-aggregated polymeric nanoparticles as tumor-homing near-infrared absorbers for photothermal therapy of cancer. Theranostics 2.9 (2012): 871-879.
2. Park, Jin Woo. Novel cyanine dyes with vinylsulfone group for labeling biomolecules. Bioconjugate chemistry 23.3 (2012): 350-362.
3. Lim, Chang-Keun. Gadolinium-coordinated elastic nanogels for in vivo tumor targeting and imaging. Biomaterials 34.28 (2013): 6846-6852.
4. Keunsoo Jeong. Poly (oxyethylene sugaramide) s: unprecedented multihydroxyl building blocks for tumor-homing nanoassembly. Journal of Materials Chemistry B 1.28 (2013): 3437-3442.
5. Lee, So Jin. TNF-α gene silencing using polymerized siRNA/thiolated glycol chitosan nanoparticles for rheumatoid arthritis. Molecular Therapy 22.2 (2014): 397-408.
6. Yoon, Hong Yeol. Photo-crosslinked hyaluronic acid nanoparticles with improved stability for in vivo tumor-targeted drug delivery. Biomaterials 34.21 (2013): 5273-5280.
7. Park, Solji. Amphiphilized poly (ethyleneimine) nanoparticles: a versatile multi-cargo carrier with enhanced tumor-homing efficiency and biocompatibility. Journal of Materials Chemistry B 3.2 (2015): 198-206.
8. Lee, Eunjung. Co-delivery of chemosensitizing siRNA and an anticancer agent via multiple monocomplexation-induced hydrophobic association. Journal of Controlled Release 210 (2015): 105-114.
9. Xu, Peisheng. Zwitterionic chitosan derivatives for pH-sensitive stealth coating. Biomacromolecules 11.9 (2010): 2352-2358.
10. 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.
11. 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.
12. Yhee, Ji Young. Tumor-targeting transferrin nanoparticles for systemic polymerized siRNA delivery in tumor-bearing mice. Bioconjugate chemistry 24.11 (2013): 1850-1860.
13. Yoon, Hong Yeol. Glycol chitosan nanoparticles as specialized cancer therapeutic vehicles: Sequential delivery of doxorubicin and Bcl-2 siRNA. Scientific reports 4 (2014).
14. 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.
15. Hollis, Christin P. In vivo investigation of hybrid paclitaxel nanocrystals with dual fluorescent probes for cancer theranostics. Pharmaceutical research 31.6 (2014): 1450-1459.
16. Koo, Heebeom. The movement of self-assembled amphiphilic polymeric nanoparticles in the vitreous and retina after intravitreal injection. Biomaterials 33.12 (2012): 3485-3493.
17. Zhu, Lei. Real-time monitoring of caspase cascade activation in living cells. Journal of controlled release 163.1 (2012): 55-62.
18. Yoon, Hong Yeol. Bioreducible hyaluronic acid conjugates as siRNA carrier for tumor targeting. Journal of Controlled Release 172.3 (2013): 653-661.
19. 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.
20. Park, Jin Woo. Wide-Ranged Fluorescent Molecular Weight Size Markers for Electrophoresis. Bulletin of the Korean Chemical Society 34.1 (2013): 29-30.
21. 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