Em 495-570 nm Green

Phalloidin CruzFluor™ 532 Conjugate is a highly specific fluorescent probe that emits light in the 495-570 nm range. This conjugate selectively binds to F-actin, stabilizing filamentous actin structures and enabling detailed visualization of cytoskeletal dynamics. Its robust photophysical properties ensure consistent signal intensity, while its unique affinity for actin facilitates the study of cellular architecture and motility, revealing intricate cellular behaviors and interactions.

Vitamin A is a fat-soluble compound that plays a crucial role in various biochemical pathways, particularly in vision and cellular differentiation. Its unique structure allows for efficient isomerization, enabling it to interact with light in the 495-570 nm range. This interaction facilitates the formation of retinoid signaling molecules, which are essential for gene expression regulation. Additionally, Vitamin A's hydrophobic nature influences its transport and storage in lipid-rich environments, impacting its bioavailability and metabolic pathways.

7-Hydroxy-4-(trifluoromethyl)coumarin exhibits remarkable fluorescence properties, particularly in the emission range of 495-570 nm. Its trifluoromethyl group enhances electron-withdrawing effects, leading to increased stability and altered photophysical behavior. This compound engages in specific π-π stacking interactions, influencing its aggregation state and luminescence efficiency. The unique hydrogen bonding capabilities of the hydroxyl group further modulate its reactivity and solubility in various solvents, making it a versatile candidate for diverse applications in chemical research.

Dansyl Chloride is a highly reactive acid chloride known for its distinctive fluorescence in the 495-570 nm range. Its sulfonamide moiety facilitates strong dipole-dipole interactions, enhancing solubility in polar solvents. The compound's electrophilic nature allows for rapid acylation reactions with amines, leading to the formation of stable dansyl derivatives. Additionally, its rigid structure promotes effective stacking interactions, influencing its photostability and emission characteristics.

3,3'-Diethyloxacarbocyanine iodide exhibits remarkable photophysical properties, particularly in the emission range of 495-570 nm. Its unique cyanine structure enables strong π-π stacking interactions, which enhance its fluorescence intensity and stability. The compound's ability to form J-aggregates under certain conditions leads to distinct spectral shifts, making it a subject of interest in studies of molecular aggregation. Additionally, its ionic nature contributes to effective solvation dynamics in various environments.

Fluorescein (free acid) is a highly fluorescent compound that exhibits vibrant emission in the 495-570 nm range due to its unique xanthene structure. Its strong intramolecular hydrogen bonding enhances photostability and influences its solubility in various solvents. The compound's ability to undergo protonation and deprotonation alters its spectral properties, allowing for dynamic shifts in fluorescence. Additionally, its propensity for forming aggregates can lead to intriguing changes in light absorption and emission characteristics.

6-Carboxyfluorescein diacetate is a fluorescent dye characterized by its ability to emit light in the 495-570 nm range, attributed to its unique structural features. The presence of carboxyl groups facilitates specific interactions with biological membranes, enhancing its permeability. Its diacetate form allows for rapid cellular uptake, where enzymatic hydrolysis converts it to a more polar, fluorescent form. This transformation is influenced by local pH and ionic strength, affecting its fluorescence intensity and stability.

Dansylamidoethyl Mercaptan is a fluorescent compound notable for its emission in the 495-570 nm range, driven by its dansyl moiety. The presence of the mercaptan group enhances its reactivity, allowing for specific thiol interactions with various substrates. This compound exhibits unique photophysical properties, including solvent-dependent fluorescence shifts, which can be influenced by hydrogen bonding and steric effects. Its distinct electronic structure contributes to its stability and reactivity in diverse chemical environments.

Acridine Orange hemi(zinc chloride) salt is a fluorescent dye characterized by its emission spectrum in the 495-570 nm range. This compound exhibits strong intercalation properties, allowing it to bind selectively to nucleic acids, which influences its fluorescence intensity. Its unique charge distribution and planar structure facilitate interactions with various biomolecules, leading to distinct photostability and enhanced quantum yield under specific conditions. The presence of zinc chloride further modulates its solubility and reactivity, impacting its behavior in complex environments.

Fluorescein di(β-D-galactopyranoside) is a fluorescent compound notable for its emission in the 495-570 nm range. This molecule features a galactopyranoside moiety that enhances its solubility and facilitates specific interactions with glycosylated targets. Its unique structure allows for efficient energy transfer and photophysical properties, resulting in high quantum yield. The compound's reactivity is influenced by its glycosidic bonds, which can undergo hydrolysis, impacting its fluorescence dynamics in various environments.