Items 141 to 150 of 198 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
6-FAM phosphoramidite | sc-363596 | 100 µmol | $132.00 | 1 | ||
6-FAM phosphoramidite exhibits remarkable fluorescence in the 495-570 nm range, attributed to its robust conjugated structure that facilitates effective light absorption and emission. This compound features a phosphoramidite group, which enhances its reactivity in nucleophilic substitution reactions, allowing for efficient incorporation into oligonucleotides. Its stability under various conditions and high quantum yield make it a compelling candidate for exploring molecular dynamics and interaction pathways in complex systems. | ||||||
Phalloidin CruzFluor™ 514 Conjugate | sc-363792 | 300 tests | $181.00 | |||
Phalloidin CruzFluor™ 514 Conjugate is a highly specific probe that binds to filamentous actin (F-actin), enabling detailed visualization of cytoskeletal structures. Its unique fluorophore emits in the 495-570 nm range, providing excellent contrast in fluorescence microscopy. The conjugate's affinity for F-actin allows for precise tracking of cellular dynamics, while its stability ensures reliable performance in various experimental conditions, making it ideal for studying cellular architecture and motility. | ||||||
Chromeo™ 505 NHS-ester | sc-364706 | 1 mg | $273.00 | |||
Chromeo™ 505 NHS-ester is a versatile fluorescent dye that exhibits strong emission in the 495-570 nm range, characterized by its efficient coupling to amine-containing biomolecules. This compound features a reactive NHS-ester group, facilitating rapid and selective conjugation through nucleophilic attack, which enhances its utility in labeling applications. Its robust photostability and distinct spectral properties allow for clear differentiation in multi-color experiments, making it an excellent choice for advanced imaging techniques. | ||||||
Chromeo™ 546 NHS-ester | sc-364710 | 1 mg | $275.00 | |||
Chromeo™ 546 NHS-ester is a highly reactive fluorescent dye that emits light in the 495-570 nm range, distinguished by its unique ability to form stable covalent bonds with amine groups. The NHS-ester moiety promotes rapid conjugation, enabling precise labeling of biomolecules. Its exceptional photostability and distinct spectral characteristics enhance signal clarity, making it ideal for complex experimental designs. The compound's efficient reaction kinetics ensure reliable performance in diverse applications. | ||||||
Chromeo™ P429 | sc-364760 | 1 mg | $650.00 | |||
Chromeo™ P429 is a specialized fluorescent dye that exhibits remarkable photophysical properties, emitting light in the 495-570 nm range. Its unique structure facilitates strong interactions with various functional groups, allowing for selective labeling. The compound's high quantum yield and exceptional stability under diverse conditions enhance its utility in complex assays. Additionally, its rapid reaction kinetics enable efficient incorporation into various substrates, ensuring consistent performance across applications. | ||||||
N-Dodecanoyl-NBD-D-erythro-dihydrosphingosine | 474943-05-0 | sc-364764 | 100 µg | $300.00 | ||
N-Dodecanoyl-NBD-D-erythro-dihydrosphingosine is a distinctive fluorescent probe characterized by its ability to emit light within the 495-570 nm spectrum. This compound features a unique hydrophobic tail that enhances membrane affinity, promoting specific localization within lipid environments. Its robust photostability and favorable spectral properties allow for effective tracking in dynamic systems. The compound's selective binding interactions facilitate detailed studies of lipid dynamics and cellular processes. | ||||||
5(6)-Caroxyrhodamine 6G ethylenediamine | sc-391065 | 1 mg | $370.00 | |||
5(6)-Carboxyrhodamine 6G ethylenediamine is a vibrant fluorescent dye known for its emission in the 495-570 nm range. This compound exhibits strong electrostatic interactions due to its charged groups, enhancing its solubility in aqueous environments. Its high quantum yield and exceptional photostability make it ideal for real-time imaging applications. The dye's unique structural features allow for specific binding to biomolecules, enabling detailed investigations of molecular interactions and dynamics. | ||||||
Lithocholyl-Lys-Fluorescein | sc-391070 | 1 mg | $370.00 | |||
Lithocholyl-Lys-Fluorescein is a fluorescent compound characterized by its emission spectrum in the 495-570 nm range. This molecule features a unique amphiphilic structure, promoting interactions with lipid membranes and enhancing its localization in biological systems. Its distinct conjugated system contributes to high fluorescence intensity and stability under various conditions. The compound's ability to form hydrogen bonds facilitates specific interactions with target molecules, making it a valuable tool for studying cellular processes. | ||||||
1,1-Dioctadecyl-3,3,3,3-tetramethylindocarbocyanine triflate | sc-391084 | 100 mg | $244.00 | |||
1,1-Dioctadecyl-3,3,3,3-tetramethylindocarbocyanine triflate is a fluorescent dye notable for its emission in the 495-570 nm range. Its unique hydrophobic tail enhances membrane affinity, allowing for effective incorporation into lipid bilayers. The compound exhibits strong photostability and a high quantum yield, making it suitable for various imaging applications. Additionally, its ability to undergo specific π-π stacking interactions can influence its photophysical properties, enhancing signal clarity in complex environments. | ||||||
MMP-3 Green™ substrate | sc-391415 | 1 mg | $592.00 | |||
MMP-3 Green™ substrate is a specialized chemical characterized by its distinct fluorescence in the 495-570 nm range. This compound features a unique structure that facilitates selective interactions with biomolecules, promoting specific binding pathways. Its robust stability under varying conditions enhances its reliability in experimental setups. The substrate's unique electronic properties allow for efficient energy transfer, optimizing its performance in diverse applications while minimizing background interference. | ||||||