Items 51 to 60 of 198 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Lucifer Yellow CH dilithium salt | 67769-47-5 | sc-215267 sc-215267A | 25 mg 100 mg | $223.00 $699.00 | 4 | |
Lucifer Yellow CH dilithium salt is a fluorescent dye notable for its vibrant emission in the 495-570 nm range. Its unique structure facilitates strong interactions with cellular components, enhancing its ability to penetrate membranes. The compound's high quantum yield and stability under various conditions make it an excellent choice for visualizing dynamic processes. Its distinct photophysical properties allow for effective energy transfer, contributing to its utility in advanced imaging techniques. | ||||||
Acridine Orange 10-nonyl bromide | 75168-11-5 | sc-214487 | 100 mg | $179.00 | 2 | |
Acridine Orange 10-nonyl bromide is a fluorescent compound characterized by its emission spectrum in the 495-570 nm range. This dye exhibits unique binding affinity to nucleic acids, enabling selective interaction with DNA and RNA. Its hydrophobic nonyl chain enhances membrane permeability, facilitating cellular uptake. The compound's photostability and ability to undergo intercalation contribute to its distinct fluorescence properties, making it suitable for probing nucleic acid dynamics in various environments. | ||||||
6-Carboxyfluorescein N-hydroxysuccinimide ester | 92557-81-8 | sc-214366 | 10 mg | $250.00 | 1 | |
6-Carboxyfluorescein N-hydroxysuccinimide ester is a fluorescent dye notable for its emission spectrum spanning 495-570 nm. This compound features a reactive N-hydroxysuccinimide group, which facilitates the formation of stable amide bonds with primary amines, enhancing its utility in labeling biomolecules. Its high quantum yield and excellent photostability make it ideal for applications requiring consistent fluorescence. Additionally, the carboxylic acid moiety contributes to its solubility in aqueous environments, promoting versatile interactions in biological systems. | ||||||
6-([4,6-Dichlorotriazin-2-yl]amino)fluorescein hydrochloride | 118357-32-7 | sc-214351 | 500 mg | $500.00 | ||
6-([4,6-Dichlorotriazin-2-yl]amino)fluorescein hydrochloride is a vibrant fluorescent compound characterized by its emission in the 495-570 nm range. The presence of the dichlorotriazine moiety allows for selective nucleophilic reactions, enhancing its reactivity towards amines and thiols. This compound exhibits strong photostability and a high extinction coefficient, making it suitable for applications requiring robust fluorescence. Its unique structure promotes specific interactions in diverse chemical environments. | ||||||
5(6)-Carboxynaphthofluorescein | 128724-35-6 | sc-210424 | 25 mg | $104.00 | ||
5(6)-Carboxynaphthofluorescein is a fluorescent dye notable for its emission spectrum spanning 495-570 nm. This compound features a carboxylic acid group that enhances solubility in aqueous environments and facilitates ionic interactions. Its unique naphthalene core contributes to strong π-π stacking, influencing aggregation behavior. The compound exhibits excellent photostability and a high quantum yield, making it suitable for various analytical applications where consistent fluorescence is essential. | ||||||
9-(2-Carboxy-2-cyanovinyl)julolidine | 142978-18-5 | sc-214425 | 5 mg | $157.00 | 1 | |
9-(2-Carboxy-2-cyanovinyl)julolidine is a fluorescent compound characterized by its emission in the 495-570 nm range. Its structure includes a julolidine moiety, which promotes strong intramolecular interactions and enhances light absorption. The presence of a carboxylic acid group allows for effective hydrogen bonding, influencing solubility and reactivity. This compound exhibits remarkable stability under light exposure, making it ideal for applications requiring reliable fluorescence. | ||||||
Ac-IETD-AFC | 211990-57-7 | sc-311276 sc-311276A | 5 mg 10 mg | $281.00 $453.00 | 1 | |
Ac-IETD-AFC is a fluorogenic substrate that emits light in the 495-570 nm range, showcasing unique interactions with caspases. Its design incorporates an acetylated peptide sequence, which facilitates selective cleavage by specific proteases, leading to enhanced fluorescence. The compound's hydrophobic characteristics contribute to its partitioning in biological membranes, while its kinetic profile reveals rapid reaction rates, making it a valuable tool for studying proteolytic activity in various environments. | ||||||
CalciFluor™ Fluo-8H, AM | sc-361827 | 1 mg | $413.00 | |||
CalciFluor™ Fluo-8H, AM is a fluorescent probe that exhibits emission in the 495-570 nm range, characterized by its ability to selectively bind to calcium ions. This compound undergoes a unique conformational change upon calcium binding, resulting in a significant increase in fluorescence intensity. Its lipophilic nature allows for efficient cellular uptake, while its rapid response to calcium fluctuations makes it an effective indicator for studying intracellular calcium dynamics and signaling pathways. | ||||||
6-Carboxyfluorescein | 3301-79-9 | sc-214365 | 100 mg | $118.00 | 3 | |
6-Carboxyfluorescein is a fluorescent dye that emits light in the 495-570 nm range, notable for its pH sensitivity and ability to form stable complexes with various metal ions. Its unique structure allows for strong interactions with biological membranes, enhancing its permeability. The compound exhibits distinct photophysical properties, including a high quantum yield and photostability, making it suitable for real-time monitoring of dynamic processes in diverse environments. | ||||||
8-Aminonaphthalene-1,3,6-trisulfonic acid disodium salt | 5398-34-5 | sc-210667 | 500 mg | $416.00 | ||
8-Aminonaphthalene-1,3,6-trisulfonic acid disodium salt is a highly soluble fluorescent compound that emits light in the 495-570 nm range. Its sulfonic acid groups enhance solvation and ionic interactions, promoting stability in aqueous environments. The compound's unique naphthalene backbone facilitates π-π stacking interactions, influencing its photophysical behavior. Additionally, it exhibits notable fluorescence quenching in the presence of specific analytes, making it a versatile tool for studying molecular interactions. | ||||||