Items 41 to 50 of 129 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
CruzFluor sm™ 2 succinimidyl ester | sc-362583 | 5 mg | $176.00 | |||
CruzFluor sm™ 2 succinimidyl ester is a highly reactive fluorescent compound that emits light in the 495-570 nm range. Its succinimidyl ester group enables rapid and selective conjugation with nucleophilic sites, enhancing specificity in labeling applications. The compound's unique photostability and low background fluorescence contribute to clear signal detection, while its efficient reaction kinetics allow for swift incorporation into various molecular frameworks, facilitating advanced studies in dynamic systems. | ||||||
5-(4,6-Dichloro-s-triazin-2-ylamino)fluorescein hydrochloride | 21811-74-5 | sc-290672 | 100 mg | $123.00 | ||
5-(4,6-Dichloro-s-triazin-2-ylamino)fluorescein hydrochloride is a vibrant fluorescent dye that exhibits strong emission in the 495-570 nm range. Its unique triazine moiety facilitates robust interactions with nucleophiles, promoting selective binding. The compound's high quantum yield and exceptional photostability make it ideal for applications requiring consistent signal intensity. Additionally, its reactivity profile allows for versatile incorporation into diverse chemical environments, enhancing analytical precision. | ||||||
3,3′-Dipropylthiadicarbocyanine iodide | 53213-94-8 | sc-209690 | 100 mg | $274.00 | 1 | |
3,3'-Dipropylthiadicarbocyanine iodide is a highly fluorescent compound characterized by its intense emission in the 495-570 nm range. Its unique thiadicarbocyanine structure enables strong π-π stacking interactions, enhancing its photophysical properties. The compound exhibits remarkable solvatochromism, allowing it to respond dynamically to changes in solvent polarity. Additionally, its extended conjugation contributes to a high molar absorptivity, making it suitable for various spectroscopic applications. | ||||||
Tetramethylrhodamine ethyl ester perchlorate | 115532-52-0 | sc-213026 | 25 mg | $126.00 | 3 | |
Tetramethylrhodamine ethyl ester perchlorate is a vibrant fluorescent dye that exhibits strong emission in the 495-570 nm range. Its unique rhodamine structure facilitates efficient intramolecular charge transfer, enhancing its brightness and stability. The compound demonstrates notable photostability and resistance to photobleaching, making it ideal for prolonged imaging applications. Additionally, its ability to form aggregates in certain conditions can influence its optical properties, providing insights into molecular interactions. | ||||||
Atto 565 NHS ester | sc-319832 | 1 mg | $206.00 | 1 | ||
Atto 565 NHS ester is a highly fluorescent compound characterized by its exceptional light absorption and emission properties within the 495-570 nm range. Its reactive NHS ester functionality enables efficient conjugation with amines, facilitating the formation of stable linkages. This compound exhibits remarkable stability under various environmental conditions, and its unique electronic structure allows for effective energy transfer processes. Additionally, Atto 565's distinct spectral properties can be influenced by solvent interactions, providing valuable insights into molecular dynamics. | ||||||
Chromeo™ P503 | sc-364758 | 1 mg | $435.00 | |||
Chromeo™ P503 is a specialized acid halide known for its unique reactivity and interaction with nucleophiles. It exhibits a distinctive electronic configuration that enhances its electrophilic character, promoting rapid acylation reactions. The compound's behavior is influenced by solvent polarity, which can modulate its reactivity and stability. Additionally, Chromeo™ P503 demonstrates intriguing photophysical properties, allowing for dynamic studies of molecular interactions and reaction kinetics in various environments. | ||||||
Tetramethylrhodamine-5-isothiocyanate | 80724-19-2 | sc-215960 | 5 mg | $220.00 | 2 | |
Tetramethylrhodamine-5-isothiocyanate is a vibrant fluorescent dye characterized by its strong absorption and emission in the 495-570 nm range. Its unique isothiocyanate group facilitates covalent bonding with amines, enabling selective labeling of biomolecules. The compound exhibits high photostability and a pronounced Stokes shift, making it ideal for tracking molecular interactions. Its distinct spectral properties allow for effective multiplexing in fluorescence applications, enhancing experimental versatility. | ||||||
Rhodamine B, hexyl ester, perchlorate | 877933-92-1 | sc-391078 | 10 mg | $156.00 | ||
Rhodamine B, hexyl ester, perchlorate is a fluorescent compound notable for its intense emission in the 495-570 nm range. Its hexyl ester moiety enhances lipophilicity, promoting membrane permeability and facilitating interactions with lipid environments. The perchlorate counterion contributes to its solubility in various organic solvents. This dye exhibits rapid reaction kinetics, allowing for swift incorporation into complex systems, while its robust photophysical properties support diverse experimental applications. | ||||||
Ethidium homodimer I solution | 61926-22-5 | sc-300519 | 500 µl | $412.00 | 1 | |
Ethidium homodimer I solution is a fluorescent dye characterized by its strong emission in the 495-570 nm range. This compound exhibits a unique ability to intercalate into double-stranded nucleic acids, leading to enhanced fluorescence upon binding. Its dimeric structure allows for increased stability and specificity in nucleic acid detection. The solution's high sensitivity and rapid binding kinetics make it ideal for real-time monitoring of nucleic acid interactions in various experimental setups. | ||||||
DY-550-avidin | sc-221567 sc-221567A | 1 mg 5 mg | $148.00 $592.00 | |||
DY-550-avidin is a fluorescent conjugate that emits light in the 495-570 nm range, showcasing remarkable affinity for biotin. Its avidin component facilitates strong, non-covalent interactions with biotinylated molecules, resulting in a stable complex. This compound exhibits unique photophysical properties, including high quantum yield and photostability, which enhance signal clarity in detection assays. Its rapid binding kinetics enable efficient labeling in various biochemical applications. | ||||||