Ex 495-570 nm Green

CruzFluor sm™ 2 azide is a distinctive chemical characterized by its exceptional fluorescence properties within the 495-570 nm spectrum. Its unique azide functional group facilitates specific interactions with target molecules, promoting selective reactivity. The compound exhibits notable stability under various conditions, allowing for consistent performance in diverse applications. Its ability to engage in unique photochemical reactions enhances its utility in studying molecular dynamics and interaction mechanisms.

CruzFluor sm™ 3 azide stands out for its remarkable photophysical characteristics, particularly its fluorescence emission in the 495-570 nm range. The presence of the azide group enables it to participate in unique click chemistry reactions, fostering rapid and selective bonding with alkyne-containing partners. This compound also demonstrates robust stability, making it suitable for various experimental conditions, while its distinct electronic properties allow for enhanced energy transfer processes, enriching studies in molecular interactions.

3,3'-Dipropylthiacarbocyanine iodide exhibits exceptional optical properties, particularly in the 495-570 nm range, where it displays strong fluorescence. Its unique structure facilitates effective stacking interactions, enhancing its photostability and allowing for efficient energy transfer in complex systems. The compound's hydrophobic nature promotes aggregation in aqueous environments, influencing its behavior in various experimental setups. Additionally, its distinct charge distribution contributes to selective binding with specific targets, making it a versatile tool in studies of molecular dynamics.

5(6)-Carboxytetramethylrhodamine is a highly fluorescent dye that exhibits remarkable photophysical properties, particularly in the 495-570 nm range. Its carboxyl group enhances solubility in polar solvents, facilitating interactions with biomolecules. The compound's rigid structure promotes efficient intramolecular charge transfer, resulting in high quantum yields. Additionally, its ability to form stable conjugates with amines allows for specific labeling in various experimental contexts, enhancing its utility in fluorescence-based assays.

Fluorescein-diacetate-5-isothiocyanate is a vibrant fluorescent compound that operates effectively within the 495-570 nm spectrum. Its isothiocyanate group enables robust covalent bonding with nucleophiles, facilitating selective labeling of proteins and other biomolecules. The compound's unique reactivity allows for rapid conjugation, while its diacetate moiety enhances membrane permeability, promoting cellular uptake. This dynamic behavior underpins its utility in various biochemical applications, showcasing its versatility in fluorescence studies.

DiIC16(3) perchlorate is a lipophilic fluorescent dye that exhibits strong emission in the 495-570 nm range. Its unique structure allows for efficient incorporation into lipid membranes, enhancing its localization in cellular environments. The compound's hydrophobic nature promotes aggregation in aqueous solutions, influencing its photophysical properties. Additionally, its high quantum yield and stability under light exposure make it suitable for dynamic imaging studies, revealing intricate cellular processes.

Chromoionophore XI is a specialized fluorescent probe that operates effectively within the 495-570 nm emission spectrum. Its unique design facilitates selective ion binding, leading to distinct fluorescence changes upon ion interaction. This compound exhibits remarkable sensitivity to environmental factors, such as pH and ionic strength, which can modulate its optical properties. The dynamic response of Chromoionophore XI to varying conditions allows for real-time monitoring of ion concentrations, making it a versatile tool for studying ion transport mechanisms.

5,6-Diamino-N,N,N',N'-tetraethyl-rhodamin is a vibrant fluorescent compound that exhibits strong emission in the 495-570 nm range. Its structure allows for effective resonance energy transfer, enhancing its luminescence properties. The compound's interactions with specific metal ions can induce significant shifts in fluorescence intensity, making it a valuable tool for probing complexation dynamics. Additionally, its stability under varying conditions contributes to its reliability in diverse experimental setups.

Eosine-5-isothiocyanate is a distinctive fluorescent dye characterized by its strong emission in the 495-570 nm range. Its unique isothiocyanate functional group facilitates selective labeling of biomolecules through covalent bonding, enhancing specificity in various assays. The compound exhibits notable photostability, allowing for prolonged observation without significant degradation. Its ability to engage in specific molecular interactions makes it a versatile choice for studying dynamic biological processes.

DAR-4M is a specialized fluorescent compound that exhibits vibrant emission within the 495-570 nm spectrum. Its unique structure allows for efficient energy transfer and robust photophysical properties, making it suitable for various analytical applications. The compound's reactivity as an acid halide enables it to participate in selective acylation reactions, enhancing its utility in synthetic pathways. Additionally, DAR-4M demonstrates remarkable stability under diverse experimental conditions, ensuring reliable performance in complex environments.