Ex 380-450 nm Violet
Items 71 to 79 of 79 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Atto 425-NHS ester | 892156-28-4 | sc-300206 | 1 mg | $92.00 | ||
Atto 425-NHS ester is a fluorescent dye that exhibits strong emission in the 380-450 nm range, making it ideal for various labeling applications. Its NHS ester functionality enables efficient coupling with amine-containing biomolecules, facilitating selective conjugation. The compound's unique structure promotes stability and minimizes photobleaching, while its hydrophilic properties enhance solubility in aqueous environments, allowing for versatile use in complex biological systems. | ||||||
1-(3-Isothiocyanatopropyl)-4-[5-(4-methoxyphenyl)-2-oxazolyl]pyridinium bromide | 1034443-41-8 | sc-287003 | 5 mg | $47.00 | ||
1-(3-Isothiocyanatopropyl)-4-[5-(4-methoxyphenyl)-2-oxazolyl]pyridinium bromide is a compound characterized by its distinctive isothiocyanate group, which facilitates nucleophilic reactions with thiols and amines. Its pyridinium moiety enhances solubility in polar solvents, while the oxazole ring contributes to its electronic properties, allowing for unique photophysical behavior. This compound exhibits notable stability under UV light, making it suitable for various experimental conditions. | ||||||
3-Carboxyumbelliferyl b-D-galactopyranoside | 64664-99-9 | sc-283698 sc-283698A | 5 mg 10 mg | $122.00 $332.00 | ||
3-Carboxyumbelliferyl β-D-galactopyranoside is a fluorescent substrate that exhibits strong emission in the 380-450 nm range, making it ideal for studying enzymatic activity. Its unique structure allows for specific interactions with β-galactosidase, leading to the release of a highly fluorescent product upon hydrolysis. The compound's carboxyumbelliferyl group enhances its photostability and solubility, facilitating real-time monitoring of enzymatic reactions in various biological assays. | ||||||
7-Diethylamino-3-[N-(2-maleimidoethyl)carbamoyl]coumarin | 156571-46-9 | sc-210608 sc-210608A | 1 mg 5 mg | $38.00 $107.00 | ||
7-Diethylamino-3-[N-(2-maleimidoethyl)carbamoyl]coumarin is a fluorescent compound that emits light in the 380-450 nm range, characterized by its unique maleimide moiety which enables selective conjugation to thiol groups. This specificity enhances its utility in probing protein interactions and dynamics. The diethylamino group contributes to its strong fluorescence and solubility, while the coumarin core provides excellent photophysical properties, making it suitable for various analytical applications. | ||||||
Cal-520™, AM | sc-477280 | 1 mg | $377.00 | 2 | ||
Cal-520™, AM is a fluorescent probe that exhibits emission in the 380-450 nm range, distinguished by its ability to selectively bind to calcium ions. The compound features a unique structure that facilitates rapid and reversible interactions with calcium, enhancing its sensitivity to fluctuations in ion concentration. Its robust photostability and high quantum yield make it an effective tool for monitoring dynamic calcium signaling in various environments, showcasing its versatility in fluorescence applications. | ||||||
bBBr (Dibromobimane) | sc-481952 | 5 mg | $94.00 | |||
Dibromobimane is a fluorescent compound that emits light in the 380-450 nm range, characterized by its unique ability to form stable adducts with thiols. This interaction leads to a significant increase in fluorescence intensity, allowing for sensitive detection of thiol-containing biomolecules. Its distinct photophysical properties, including high quantum yield and excellent photostability, enable precise monitoring of redox states and thiol dynamics in complex biological systems. | ||||||
Suc-Leu-Leu-Val-Tyr-AMC | 94367-21-2 | sc-471159 sc-471159A sc-471159B | 5 mg 25 mg 100 mg | $145.00 $480.00 $1500.00 | 3 | |
Suc-Leu-Leu-Val-Tyr-AMC is a fluorogenic peptide substrate that exhibits fluorescence in the 380-450 nm range. Its unique structure allows for selective cleavage by specific proteases, resulting in a marked increase in fluorescence upon enzymatic activity. This property facilitates real-time monitoring of proteolytic processes. The compound's stability and sensitivity to enzymatic interactions make it a valuable tool for studying protease kinetics and substrate specificity in various biochemical assays. | ||||||
DEAC,SE | 139346-57-9 | sc-495737 | 25 mg | $121.00 | ||
DEAC,SE is a versatile acid halide characterized by its reactivity and ability to form stable intermediates through nucleophilic acyl substitution. Its unique electronic structure enhances electrophilicity, promoting rapid reaction kinetics with amines and alcohols. This compound exhibits distinct solubility properties, allowing for efficient incorporation into various organic synthesis pathways. Additionally, DEAC,SE's ability to participate in coupling reactions makes it a key player in generating complex molecular architectures. | ||||||
7-Hydroxycoumarin-3-carboxylic acid, succinimidyl ester | sc-495740 | 50 mg | $119.00 | |||
7-Hydroxycoumarin-3-carboxylic acid, succinimidyl ester is a reactive compound known for its ability to facilitate acylation reactions through its electrophilic succinimidyl group. This ester exhibits strong fluorescence under UV light, making it useful for tracking molecular interactions. Its unique structure allows for selective binding with nucleophiles, leading to the formation of stable conjugates. The compound's solubility profile enhances its compatibility in diverse organic reactions, promoting efficient synthesis pathways. | ||||||