Items 11 to 20 of 198 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
FlAsH-EDT2 | 212118-77-9 | sc-363644 sc-363644A sc-363644B | 25 mg 100 mg 1 g | $490.00 $1498.00 $9364.00 | 5 | |
FlAsH-EDT2 is a specialized fluorescent probe that exhibits remarkable selectivity for specific protein interactions, particularly with tetracysteine motifs. Emitting light in the 495-570 nm range, it undergoes a unique reaction mechanism that involves covalent bonding, leading to enhanced fluorescence upon binding. This compound's distinct photophysical properties, including high quantum yield and photostability, make it an exceptional tool for probing molecular dynamics and cellular localization in real-time studies. | ||||||
Lucigenin | 2315-97-1 | sc-202698 sc-202698A sc-202698B sc-202698C | 10 mg 50 mg 500 mg 1 g | $30.00 $54.00 $179.00 $308.00 | 17 | |
Lucigenin is a luminescent compound that emits light in the 495-570 nm range, characterized by its unique ability to interact with reactive oxygen species. Its distinct electron transfer properties facilitate the generation of singlet oxygen, influencing various biochemical pathways. The compound exhibits notable stability under varying conditions, allowing for consistent fluorescence. Additionally, its specific binding affinity to certain metal ions enhances its photophysical behavior, making it a valuable tool for studying redox processes. | ||||||
FURA 2/AM | 108964-32-5 | sc-203052 sc-203052A sc-203052B | 50 µg 1 mg 50 mg | $33.00 $149.00 $3951.00 | 17 | |
FURA 2/AM is a fluorescent probe that exhibits excitation and emission in the 495-570 nm range, primarily utilized for monitoring intracellular calcium levels. Its unique esterified form allows for cell permeability, enabling real-time imaging of calcium dynamics. Upon de-esterification within cells, it binds calcium ions, resulting in a significant increase in fluorescence intensity. This property facilitates the exploration of calcium signaling pathways and cellular responses to stimuli, providing insights into various physiological processes. | ||||||
FURA-PE3/AM | 172890-84-5 | sc-203960 | 50 µg | $77.00 | 1 | |
FURA-PE3/AM is a fluorescent indicator that operates within the 495-570 nm range, designed for the detection of intracellular calcium fluctuations. Its distinctive acetoxymethyl (AM) ester form enhances cellular uptake, allowing for effective visualization of calcium interactions. Upon hydrolysis, the probe reveals a marked increase in fluorescence upon binding calcium ions, enabling detailed studies of calcium-mediated signaling pathways and cellular behavior under various conditions. | ||||||
BCECF/AM | 117464-70-7 | sc-202492 | 1 mg | $123.00 | 6 | |
BCECF/AM is a fluorescent probe that emits light in the 495-570 nm range, primarily utilized for monitoring pH changes within cells. Its unique acetoxymethyl ester modification facilitates membrane permeability, allowing for efficient intracellular accumulation. Once inside the cell, hydrolysis occurs, converting it to a free acid form that exhibits a significant fluorescence shift in response to pH variations, making it an effective tool for studying cellular acid-base dynamics and metabolic processes. | ||||||
Fluorescein sodium salt | 518-47-8 | sc-206026 sc-206026A sc-206026B sc-206026C | 100 g 500 g 1 kg 5 kg | $53.00 $155.00 $245.00 $767.00 | 8 | |
Fluorescein sodium salt is a highly fluorescent compound that exhibits vibrant emission in the 495-570 nm range, characterized by its strong light absorption and rapid photophysical transitions. Its unique structure allows for efficient resonance energy transfer, enhancing its brightness. The compound's anionic form facilitates interactions with cationic species, leading to distinct aggregation behaviors in various environments. Additionally, its solubility in aqueous solutions promotes versatile applications in fluorescence-based assays. | ||||||
3,3′-Dihexyloxacarbocyanine Iodide | 53213-82-4 | sc-205905 | 250 mg | $87.00 | 6 | |
3,3′-Dihexyloxacarbocyanine Iodide is a lipophilic dye known for its striking fluorescence in the 495-570 nm range. Its unique cyanine structure enables strong π-π stacking interactions, which can influence its photostability and emission characteristics. The compound exhibits notable solvatochromism, with its spectral properties varying significantly in different solvent environments. This behavior is attributed to intramolecular charge transfer, making it sensitive to local polarity changes. | ||||||
5-Carboxyfluorescein-N-hydroxysuccinimide Ester | 92557-80-7 | sc-210302 | 25 mg | $456.00 | ||
5-Carboxyfluorescein-N-hydroxysuccinimide Ester is a fluorescent probe that exhibits vibrant emission in the 495-570 nm range. Its reactivity stems from the N-hydroxysuccinimide moiety, which facilitates efficient conjugation to amine-containing biomolecules. This compound demonstrates exceptional stability under physiological conditions and exhibits a high quantum yield, making it ideal for tracking molecular interactions. Its unique structure allows for specific binding, enhancing its utility in various biochemical applications. | ||||||
Lucifer Yellow VS dilithium salt | 71231-14-6 | sc-215269 sc-215269A | 25 mg 100 mg | $250.00 $595.00 | 4 | |
Lucifer Yellow VS dilithium salt is a fluorescent dye characterized by its striking emission spectrum in the 495-570 nm range. This compound features a unique sulfonate group that enhances solubility and facilitates strong ionic interactions with biological substrates. Its photostability and high extinction coefficient contribute to its effectiveness in visualizing cellular processes. The dye's distinct molecular architecture allows for selective binding, enabling detailed studies of dynamic biological systems. | ||||||
2′,7′-Dichlorodihydrofluorescein Diacetate | 4091-99-0 | sc-359840 sc-359840A sc-359840B | 100 mg 250 mg 500 mg | $124.00 $286.00 $416.00 | 40 | |
2′,7′-Dichlorodihydrofluorescein Diacetate is a fluorescent probe notable for its emission in the 495-570 nm range. This compound undergoes deacetylation in biological environments, leading to enhanced fluorescence upon cellular uptake. Its unique dichlorofluorescein structure allows for specific interactions with reactive oxygen species, making it a valuable tool for studying oxidative stress. The compound's high quantum yield and stability under various conditions further enhance its utility in fluorescence-based applications. | ||||||