Ex 450-495 nm Blue

Fluorescent Red Mega 485 NHS-ester exhibits remarkable photophysical properties, particularly in the 450-495 nm excitation range. Its NHS-ester moiety enables efficient amine coupling, promoting specific interactions with biomolecules. The compound's high quantum yield and stability under various conditions enhance its utility in fluorescence applications. Additionally, its unique structural design allows for versatile conjugation pathways, facilitating the formation of diverse fluorescent conjugates.

Calcein, UltraPure Grade, is a highly fluorescent compound that exhibits strong emission in the 450-495 nm range. Its unique chelating properties allow it to form stable complexes with metal ions, influencing reaction kinetics and enhancing fluorescence intensity. The compound's robust photostability ensures consistent performance in various environments, while its distinct molecular structure facilitates selective interactions with an array of substrates, making it a versatile tool in fluorescence studies.

Flutax 1 is a distinctive acid halide characterized by its reactivity and ability to engage in nucleophilic acyl substitution reactions. Its unique electronic configuration enhances electrophilicity, promoting rapid interactions with amines and alcohols. The compound's hydrophobic nature influences solubility and partitioning behavior, while its specific steric properties can dictate reaction pathways. Additionally, Flutax 1's stability under varying conditions allows for controlled reactivity in synthetic applications.

5-FAM ethylenediamine is a notable compound that exhibits strong fluorescence properties, particularly in the 450-495 nm range. Its unique structure facilitates specific interactions with biomolecules, enhancing its ability to form stable complexes. The compound's dual amine functionality allows for versatile bonding with various substrates, influencing reaction kinetics. Additionally, its hydrophilic characteristics contribute to solubility in aqueous environments, impacting its behavior in diverse chemical contexts.

5(6)-FAM cadaverine is a fluorescent compound that exhibits remarkable stability and specificity in molecular interactions, particularly within the 450-495 nm excitation range. Its unique cadaverine backbone enhances binding affinity to various biological targets, promoting effective energy transfer processes. The presence of multiple amine groups facilitates diverse hydrogen bonding and electrostatic interactions, influencing its reactivity and solubility in polar solvents, thus broadening its applicability in biochemical studies.

DiOC16(3) perchlorate is a fluorescent dye characterized by its strong emission properties within the 450-495 nm range. Its unique structure allows for effective membrane partitioning, enhancing its ability to interact with lipid bilayers. The compound's hydrophobic tail promotes aggregation in nonpolar environments, while its perchlorate group contributes to ionic interactions, influencing its solubility and stability. This behavior facilitates dynamic cellular imaging and tracking in various experimental setups.

DiOC3(3) iodide is a fluorescent dye notable for its vibrant emission in the 450-495 nm spectrum. Its unique amphiphilic structure enables efficient incorporation into cellular membranes, where it exhibits selective binding to lipid domains. The compound's iodide moiety enhances its photostability and influences its interaction with polar and nonpolar environments. This property allows for distinct fluorescence characteristics, making it suitable for probing membrane dynamics and cellular architecture.

PerCP, a peridinin-chlorophyll-protein complex, exhibits remarkable fluorescence in the 450-495 nm range, driven by its unique protein-bound chlorophyll structure. This complex facilitates energy transfer through specific molecular interactions, enhancing light absorption and emission efficiency. Its distinct photophysical properties allow it to participate in photosynthetic pathways, where it plays a crucial role in capturing light energy and transferring it to reaction centers, influencing overall photosynthetic efficiency.

5(6)-FAM Mixed Isomers is a fluorescent dye characterized by its vibrant emission in the 450-495 nm range. Its unique structure allows for strong interactions with biomolecules, enhancing its photostability and quantum yield. The dye's ability to form non-covalent complexes facilitates specific binding to target molecules, making it an effective probe for studying molecular dynamics. Its distinct spectral properties enable precise tracking in various experimental conditions, revealing intricate biological processes.

Lucigenin is a highly pure chemiluminescent compound that exhibits notable fluorescence in the 450-495 nm range. Its unique electron-rich structure promotes efficient energy transfer and enhances its reactivity with reactive oxygen species. This property allows for distinct pathways in redox reactions, leading to the generation of light upon interaction with specific substrates. Additionally, Lucigenin's robust photophysical characteristics contribute to its stability under varying experimental conditions, making it a versatile tool for probing molecular interactions.