FSD Fluor™ 750 NHS ester
Cat. No. List below
Description
FSD Fluor™ 750 NHS ester is a cutting-edge, amine-reactive near-infrared (NIR) fluorescent dye developed by BioActs. This next-generation dye offers superior optical properties compared to spectrally similar fluorophores, making it an ideal choice for a wide range of biochemical and biological analytical applications. Applications of FSD Fluor™ 750 include invitro imaging (Conjugated primary and secondary antibodies serve as molecular probes), In Vivo NIR Imaging (Optimized for labeling antibodies, peptides, proteins, and ligands), amine-modified oligonucleotide labeling in molecular biology, protein tagging and cellular imaging in cell biology and in medical imaging for deep tissue penetration for non-invasive diagnostics. FSD Fluor™ 750 is compatible with most common fluorescence imaging systems, including:Confocal microscopes with 750 nm laser excitation; Flow cytometers with red laser (633 nm) excitation; and In vivo imaging systems with NIR capabilities.
Some key features are:
Exceptional Brightness: With an extinction coefficient of ≥200,000 cm?¹M?¹, FSD Fluor™ 750 delivers outstanding fluorescence intensity after binding to biomolecules.
Optimal Spectral Properties: Excitation/Emission maxima at 751/774 nm, similar to Alexa 750, Cy7, IRDye 750, and DyLight 755.
Versatile Applications: Ideal for single-molecule detection, fluorescence correlation spectroscopy, and fluorescence polarization measurements.
Tissue Penetration: Emission in the NIR region allows for deep tissue imaging.
Advantages Over Similar Dyes:
Enhanced Stability: Dye-protein conjugates show improved photostability.
Superior Brightness: Up to 1.5x brighter than spectrally similar dyes in protein conjugates.
Reduced Background: Lower non-specific binding, resulting in improved signal-to-noise ratios.
Specifications
- Fluorophore: FSD Fluor™ 750
- Reactive group: NHS ester
- Excitation/Emission Max.(nm): 751/774
- Spectrally similar dyes: Alexa750, DyLight755, Cy7, IRDye750
- Extinction coefficient: ≥ 200,000 cm-1M-1
- CF280: 0.03
- Appearance: Green Liquid
- Molecular Weight: 1294.35 g/mol
- Solubility: DMF, DMSO
- 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™ 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.
Key Benefits:
- Superior brightness: up to 30% brighter than leading competitors, enabling detection fo low-abundance targets.
- Excellent Stability: Maintains high fluorescence intensity after bioconjugation
- Versatile Applications: Ideal for antibody labeling, nucleic acid detection, and protein studies
- Optimized for Single-Molecule Detection: Perfect for fluorescence correlation spectroscopy and polarization measurements
- Higher quantum yield comparing to traditional dyes
- Equipped with variety of reactive group
- Covering the full fluorescence spectral range from visible to NIR
- Enhanced Sensitivity: Detect targets with greater accuracy, even at low concentrations
- Reduced Background: Higher signal-to-noise ratio for clearer images and more reliable data
- Cost-Effective: Achieve superior results with less dye, maximizing your research budget
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. 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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