Items 51 to 60 of 129 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Atto 520-Biotin | sc-300207 | 1 mg | $75.00 | |||
Atto 520-Biotin is a fluorescent dye that emits light within the 495-570 nm spectrum, characterized by its exceptional binding affinity to biotin. This compound features a unique structure that promotes specific interactions with biotinylated targets, leading to the formation of stable complexes. Its distinct photophysical properties, including enhanced brightness and stability under illumination, contribute to improved signal resolution in various analytical techniques. The rapid association kinetics of Atto 520-Biotin facilitate efficient labeling, making it a versatile tool in biochemical research. | ||||||
N-(6-Aminohexyl)rhodamine 6G-amide bis(trifluoroacetate) | 1140505-40-3 | sc-301226 | 10 mg | $141.00 | ||
N-(6-Aminohexyl)rhodamine 6G-amide bis(trifluoroacetate) is a fluorescent compound that emits light in the 495-570 nm range, distinguished by its robust interaction with amine groups. This dye exhibits unique photostability and high quantum yield, allowing for prolonged observation without significant photobleaching. Its structural design enables effective energy transfer and resonance effects, enhancing fluorescence intensity. The compound's reactivity as an acid halide facilitates selective conjugation with various substrates, promoting diverse applications in molecular imaging and detection. | ||||||
N-(8-Amino-3,6-dioxaoctyl)rhodamine 6G-amide bis(trifluoroacetate) | sc-301228 sc-301228A | 10 mg 50 mg | $104.00 $462.00 | |||
N-(8-Amino-3,6-dioxaoctyl)rhodamine 6G-amide bis(trifluoroacetate) is a vibrant fluorescent dye that emits in the 495-570 nm range, characterized by its unique dioxaoctyl chain which enhances solubility and molecular flexibility. This compound exhibits exceptional photophysical properties, including high extinction coefficients and efficient energy transfer mechanisms. Its acid halide functionality allows for versatile coupling reactions, enabling tailored modifications for specific interactions in complex environments. | ||||||
N-[2-(2-Aminoethylamino)ethyl]rhodamine 6G-amide bis(trifluoroacetate) | sc-301259 | 10 mg | $106.00 | |||
N-[2-(2-Aminoethylamino)ethyl]rhodamine 6G-amide bis(trifluoroacetate] is a striking fluorescent compound that emits light in the 495-570 nm spectrum. Its unique structure features a flexible aminoethylamino chain, which facilitates strong intermolecular interactions and enhances its photostability. The presence of trifluoroacetate groups contributes to its solubility in various solvents, while its acid halide characteristics enable selective reactivity, making it suitable for diverse chemical transformations. | ||||||
Atto 565-Biotin | sc-319833 | 1 mg | $171.00 | |||
Atto 565-Biotin is a vibrant fluorescent dye that emits light in the 495-570 nm range, characterized by its unique biotin moiety, which allows for specific binding interactions with avidin or streptavidin. This compound exhibits exceptional photostability and a high quantum yield, making it ideal for sensitive detection applications. Its hydrophilic properties enhance solubility in aqueous environments, facilitating versatile labeling and tracking in various biochemical assays. | ||||||
Phalloidin CruzFluor™ 532 Conjugate | sc-363793 | 300 tests | $186.00 | |||
Phalloidin CruzFluor™ 532 Conjugate is a specialized fluorescent probe that selectively binds to F-actin, enabling detailed visualization of cytoskeletal structures. Emitting light in the 495-570 nm range, it showcases remarkable photostability and a high signal-to-noise ratio. This conjugate's unique affinity for filamentous actin allows for precise imaging of cellular dynamics, enhancing the understanding of cellular architecture and motility in various biological contexts. | ||||||
4-Dimethylamino-4′-nitrostilbene | 2844-15-7 | sc-214235 | 500 mg | $124.00 | ||
4-Dimethylamino-4'-nitrostilbene is a notable organic compound characterized by its strong fluorescence in the 495-570 nm range. Its unique electron-donating dimethylamino group enhances its photophysical properties, leading to efficient light absorption and emission. The nitro group introduces significant electron-withdrawing effects, influencing its reactivity and interaction with various solvents. This compound exhibits distinct solvatochromic behavior, making it valuable for studying solvent effects on fluorescence. | ||||||
Acridine Orange hemi(zinc chloride) salt | 10127-02-3 | sc-214488 sc-214488A | 10 g 25 g | $62.00 $79.00 | 1 | |
Acridine Orange hemi(zinc chloride) salt is a fluorescent compound that exhibits remarkable photostability and a broad emission spectrum, particularly in the 495-570 nm range. Its unique structure allows for intercalation with nucleic acids, facilitating specific binding interactions. The presence of zinc enhances its luminescent properties, while the salt form contributes to improved solubility in various media. This compound also demonstrates distinct pH-dependent fluorescence, making it an intriguing subject for studying molecular interactions in diverse environments. | ||||||
Resorufin sodium salt | 34994-50-8 | sc-206019 sc-206019A sc-206019B | 500 mg 1 g 5 g | $250.00 $374.00 $1431.00 | 5 | |
Resorufin sodium salt is a highly fluorescent compound characterized by its vibrant emission in the 495-570 nm range. Its unique structure enables efficient electron transfer processes, leading to rapid reaction kinetics in various biochemical assays. The compound's anionic nature enhances solubility in aqueous environments, promoting interactions with proteins and other biomolecules. Additionally, Resorufin exhibits notable sensitivity to environmental changes, making it a valuable tool for probing dynamic molecular interactions. | ||||||
Oxonol VI | 64724-75-0 | sc-212489 | 100 mg | $415.00 | ||
Oxonol VI is a distinctive dye known for its strong fluorescence within the 495-570 nm spectrum. Its unique molecular structure facilitates specific interactions with lipid membranes, allowing it to act as a probe for membrane potential changes. The compound exhibits rapid photophysical responses, influenced by its environment, which can alter its emission properties. This sensitivity to ionic strength and pH variations enhances its utility in studying membrane dynamics and cellular processes. | ||||||