Ex 495-570 nm Green

CruzQuench™ 3 amine is a distinctive compound known for its robust hydrogen bonding capabilities and unique steric effects. Its molecular structure facilitates specific interactions with electrophiles, leading to tailored reactivity profiles. The compound demonstrates remarkable solubility in various solvents, enhancing its versatility in synthetic applications. Additionally, its ability to stabilize transition states contributes to efficient reaction pathways, making it a noteworthy choice for complex chemical processes.

CruzQuench™ 3 CPG 500 Å is characterized by its exceptional photophysical properties, particularly its fluorescence emission in the 495-570 nm range. This compound exhibits unique interactions with light, leading to enhanced quantum yields and stability under excitation. Its structural design promotes effective energy transfer mechanisms, allowing for distinct pathways in photochemical reactions. The material's high surface area and porosity further optimize its performance in various applications, making it a compelling choice for advanced chemical systems.

Phalloidin CruzFluor™ 514 Conjugate is distinguished by its ability to selectively bind to filamentous actin, facilitating the visualization of cytoskeletal structures. Its fluorescence emission in the 495-570 nm range is enhanced by specific molecular interactions that stabilize the conjugate, resulting in robust signal intensity. The compound's unique structural features promote effective binding kinetics, allowing for precise tracking of dynamic cellular processes and enhancing imaging resolution in complex biological systems.

Chromeo™ 505 NHS-ester is characterized by its reactive NHS-ester functionality, which enables efficient coupling with amine-containing biomolecules. This compound exhibits a distinct fluorescence emission in the 495-570 nm range, attributed to its unique chromophore structure. The rapid reaction kinetics facilitate swift conjugation, while its stability under physiological conditions ensures reliable performance in various applications. Its selective reactivity enhances specificity in labeling, making it a versatile tool for probing molecular interactions.

Chromeo™ 546 NHS-ester features a highly reactive NHS-ester group, promoting targeted conjugation with amines. Its fluorescence emission in the 495-570 nm range is a result of a carefully designed chromophore, which enhances visibility in complex environments. The compound demonstrates exceptional stability, allowing for prolonged interactions without degradation. Its unique reactivity profile enables precise labeling, making it ideal for studying intricate molecular dynamics and interactions.

Chromeo™ P540 is characterized by its distinctive reactivity as an acid halide, facilitating rapid acylation reactions with nucleophiles. Its fluorescence emission within the 495-570 nm spectrum is attributed to a specialized chromophore structure, which enhances its photostability and minimizes quenching effects. This compound exhibits unique kinetic properties, allowing for efficient and selective labeling of biomolecules, thereby enabling detailed exploration of molecular interactions and pathways.

Chromeo™ P543 stands out for its exceptional ability to engage in electrophilic acylation, showcasing a unique affinity for specific nucleophiles. Its fluorescence emission in the 495-570 nm range is driven by a tailored chromophore that enhances its stability under various conditions. The compound's distinctive reaction kinetics allow for precise modulation of reaction rates, making it an intriguing candidate for studying complex molecular dynamics and interactions in diverse environments.

5(6)-Carboxyrhodamine 6G ethylenediamine exhibits remarkable photophysical properties, characterized by its strong fluorescence in the 495-570 nm range. This compound demonstrates unique interactions with metal ions, leading to enhanced luminescence and potential shifts in emission spectra. Its robust structure allows for effective energy transfer processes, making it a valuable tool for probing molecular environments and understanding dynamic interactions in various chemical systems.

1,1-Dioctadecyl-3,3,3,3-tetramethylindocarbocyanine triflate is a highly fluorescent dye that exhibits exceptional stability and solubility in organic solvents. Its unique structure facilitates strong π-π stacking interactions, which can influence aggregation behavior and fluorescence intensity. The compound's distinct absorption and emission characteristics enable it to serve as a sensitive probe for studying lipid membranes and other complex environments, revealing insights into molecular dynamics and interactions.

MMP-3 Green™ substrate is a specialized chemical that exhibits remarkable photophysical properties, particularly in the 495-570 nm range. Its unique molecular architecture allows for selective interactions with specific biomolecules, enhancing its reactivity. The substrate's ability to undergo rapid electron transfer processes contributes to its dynamic behavior in various environments, making it an effective tool for probing intricate biochemical pathways and reaction kinetics.