Items 1 to 10 of 31 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
ADHP | 119171-73-2 | sc-291898 | 25 mg | $507.00 | 1 | |
ADHP is a distinctive acid halide known for its reactivity and ability to form stable intermediates through nucleophilic acyl substitution. Its unique electronic structure promotes rapid reaction kinetics, making it an efficient acylating agent. The compound exhibits strong dipole interactions, enhancing its solubility in polar solvents. Additionally, ADHP's propensity to engage in specific molecular interactions allows for the formation of diverse derivatives, expanding its utility in synthetic pathways. | ||||||
Phalloidin CruzFluor™ 594 Conjugate | sc-363795 | 300 tests | $184.00 | 23 | ||
Phalloidin CruzFluor™ 594 Conjugate is a specialized fluorescent probe that selectively binds to F-actin, facilitating the visualization of cytoskeletal structures. Its unique conjugation with the CruzFluor™ 594 dye enables excitation at 570-590 nm, producing bright fluorescence. This compound exhibits high affinity for actin filaments, allowing for precise imaging of cellular dynamics. Its stability and low photobleaching make it ideal for long-term studies in fluorescence microscopy. | ||||||
7-Ethoxyresorufin | 5725-91-7 | sc-200606 sc-200606A | 2 mg 10 mg | $138.00 $270.00 | 6 | |
7-Ethoxyresorufin is a fluorescent compound characterized by its unique ability to undergo specific molecular interactions that enhance its photophysical properties. Excitable within the 570-590 nm range, it exhibits distinct reaction kinetics, particularly in enzymatic assays, where it serves as a substrate for cytochrome P450 enzymes. Its structural features allow for selective binding and transformation, making it a valuable tool for studying metabolic pathways and enzyme activity in various biological systems. | ||||||
Resorufin | 635-78-9 | sc-206039 sc-206039B | 1 g 5 g | $270.00 $823.00 | 2 | |
Resorufin is a highly fluorescent compound notable for its exceptional photostability and sensitivity to environmental changes. Emitting light in the 570-590 nm range, it engages in unique electron transfer processes, facilitating rapid redox reactions. Its structural configuration promotes specific interactions with various biomolecules, allowing for the exploration of metabolic dynamics and cellular responses. The compound's distinct optical properties make it a key player in fluorescence-based assays and studies of biochemical pathways. | ||||||
Sulforhodamine 101 | 60311-02-6 | sc-215929 sc-215929A | 50 mg 100 mg | $92.00 $169.00 | 4 | |
Sulforhodamine 101 is a vibrant fluorescent dye characterized by its strong absorption and emission in the 570-590 nm range. Its unique structure allows for robust interactions with proteins and nucleic acids, enhancing its utility in various analytical applications. The compound exhibits remarkable stability under light exposure, enabling prolonged observation in dynamic systems. Additionally, its high quantum yield and low background fluorescence contribute to its effectiveness in detecting subtle changes in molecular environments. | ||||||
5-Carboxy-X-rhodamine N-succinimidyl ester | 344402-35-3 | sc-214317 sc-214317A | 5 mg 100 mg | $390.00 $1821.00 | ||
5-Carboxy-X-rhodamine N-succinimidyl ester is a highly fluorescent compound that exhibits strong excitation and emission in the 570-590 nm range. Its reactive N-succinimidyl ester group facilitates efficient conjugation with amine-containing biomolecules, promoting specific labeling. The dye's unique carboxylic acid functionality enhances solubility in aqueous environments, while its robust photostability allows for reliable imaging over extended periods. This compound's distinct spectral properties make it ideal for discerning intricate molecular interactions. | ||||||
Resorufin benzyl ether | 87687-02-3 | sc-208301 sc-208301A | 5 mg 10 mg | $100.00 $169.00 | 1 | |
Resorufin benzyl ether is a fluorescent compound characterized by its vibrant emission in the 570-590 nm range. Its unique ether linkage enhances lipophilicity, allowing for selective partitioning in lipid environments. The compound undergoes rapid de-esterification, leading to the formation of resorufin, which exhibits heightened fluorescence. This transformation is influenced by pH and ionic strength, making it a valuable tool for studying dynamic molecular processes and interactions in various environments. | ||||||
CruzQuench™ 3 maleimide | sc-362645 | 5 mg | $234.00 | |||
CruzQuench™ 3 maleimide is a specialized fluorescent probe that emits light in the 570-590 nm range, distinguished by its maleimide functional group, which facilitates selective thiol labeling. This compound exhibits unique reactivity with sulfhydryl groups, enabling specific covalent bond formation. Its stability under varying conditions and rapid reaction kinetics make it an effective tool for probing molecular interactions, enhancing the understanding of biochemical pathways and cellular dynamics. | ||||||
Resorufin pentyl ether | 87687-03-4 | sc-208304 sc-208304A | 1 mg 5 mg | $204.00 $632.00 | 2 | |
Resorufin pentyl ether is a fluorescent compound that emits light in the 570-590 nm range, characterized by its ether linkage which enhances solubility and stability in various environments. This compound undergoes rapid electron transfer processes, leading to efficient fluorescence. Its unique structural features allow for specific interactions with biological molecules, making it a valuable tool for studying dynamic cellular processes and molecular interactions in real-time. | ||||||
Resorufin methyl ether | 5725-89-3 | sc-208303 sc-208303A | 1 mg 5 mg | $62.00 $213.00 | 1 | |
Resorufin methyl ether is a fluorescent dye that exhibits strong emission in the 570-590 nm range, attributed to its unique conjugated system. The presence of the methyl ether group enhances its hydrophobicity, facilitating membrane permeability. This compound engages in rapid photophysical processes, including excited-state intramolecular proton transfer, which contributes to its distinct fluorescence properties. Its structural design allows for selective interactions with various substrates, influencing reaction kinetics and pathways in diverse chemical environments. | ||||||