Items 41 to 50 of 108 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Fluorescein-dUTP | 214154-36-6 | sc-391125 | 25 nmol | $370.00 | ||
Fluorescein-dUTP is a modified nucleotide that incorporates a fluorescein moiety, enabling it to emit bright fluorescence when excited at 450-495 nm. This compound exhibits high affinity for DNA polymerases, facilitating incorporation into nucleic acid strands during replication. Its distinct photostability and low background fluorescence make it ideal for real-time monitoring of nucleic acid synthesis, providing insights into molecular dynamics and interactions in biological systems. | ||||||
MTSEA-Fluorescein | 1356019-48-1 | sc-218892 | 5 mg | $374.00 | 1 | |
MTSEA-Fluorescein is a fluorescent probe characterized by its unique ability to form covalent bonds with thiol groups, enhancing its specificity in labeling proteins. When excited at 450-495 nm, it exhibits strong fluorescence, allowing for precise tracking of molecular interactions. Its rapid reaction kinetics with cysteine residues enable real-time observation of conformational changes in proteins, making it a powerful tool for studying protein dynamics and interactions in various biochemical pathways. | ||||||
PerCP | sc-359908 sc-359908A | 1 mg 50 mg | $122.00 $3124.00 | 1 | ||
PerCP is a fluorescent dye characterized by its unique spectral properties, particularly its emission in the 450-495 nm range. It exhibits strong photostability and minimal photobleaching, making it ideal for long-term imaging applications. The dye's molecular structure allows for effective resonance energy transfer, enhancing its brightness. Additionally, PerCP's hydrophilic nature facilitates its incorporation into various biological systems, enabling precise tracking of cellular processes and interactions. | ||||||
CalciFluor™ Fluo-8, sodium salt | sc-362562A sc-362562 | 500 µg 1 mg | $254.00 $369.00 | 1 | ||
CalciFluor™ Fluo-8, sodium salt, is a fluorescent probe that exhibits remarkable sensitivity to calcium ions, emitting light in the 450-495 nm range. Its unique design allows for rapid binding to calcium, facilitating real-time monitoring of intracellular calcium dynamics. The compound's high quantum yield and low background fluorescence enhance signal clarity, while its water solubility promotes efficient cellular uptake, making it a powerful tool for studying calcium signaling pathways. | ||||||
3,3′-Diethyloxacarbocyanine iodide | 905-96-4 | sc-214157 | 1 g | $119.00 | ||
3,3'-Diethyloxacarbocyanine iodide is a highly fluorescent compound that emits light in the 450-495 nm range, distinguished by its unique oxacarbocyanine structure. This dye exhibits strong solvatochromism, where its fluorescence properties shift based on the solvent environment, allowing for versatile applications in various media. Its robust molecular interactions, including hydrogen bonding and electrostatic interactions, contribute to its stability and enhanced brightness, making it a valuable tool for probing dynamic biological systems. | ||||||
Fluorescein (free acid) | 2321-07-5 | sc-215040 sc-215040A sc-215040B | 2.5 g 100 g 250 g | $31.00 $50.00 $112.00 | 1 | |
Fluorescein (free acid) is a vibrant fluorescent dye that emits light in the 450-495 nm range, characterized by its unique xanthene structure. It exhibits notable photostability and high quantum yield, making it ideal for various applications. The compound's strong intermolecular interactions, such as π-π stacking and hydrogen bonding, enhance its solubility in aqueous environments. Additionally, its pH sensitivity allows for distinct fluorescence changes, providing insights into local chemical environments. | ||||||
6-Carboxyfluoresceine diacetate | 3348-03-6 | sc-207102 sc-207102A | 25 mg 100 mg | $80.00 $202.00 | ||
6-Carboxyfluorescein diacetate is a fluorescent compound that exhibits strong emission in the 450-495 nm range, attributed to its unique structural features. This dye is notable for its ability to undergo hydrolysis, releasing the free acid form, which enhances its fluorescence properties. Its lipophilic diacetate groups facilitate cellular permeability, while the carboxylate moiety enables specific interactions with biological macromolecules, influencing its reactivity and fluorescence intensity in various environments. | ||||||
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 emits light in the 450-495 nm range, characterized by its unique intercalation properties. This dye can bind to nucleic acids, leading to enhanced fluorescence upon complex formation. Its zwitterionic nature allows for versatile interactions with various substrates, while the presence of zinc ions can influence its photostability and reaction kinetics, making it a dynamic probe in diverse chemical environments. | ||||||
Fluorescein di(β-D-galactopyranoside) | 17817-20-8 | sc-221617 sc-221617B sc-221617A sc-221617C sc-221617D sc-221617E | 1 mg 2 mg 5 mg 10 mg 25 mg 50 mg | $89.00 $114.00 $212.00 $385.00 $877.00 $1574.00 | 1 | |
Fluorescein di(β-D-galactopyranoside) is a fluorescent compound that exhibits emission in the 450-495 nm range, notable for its specific glycosidic interactions. This compound undergoes hydrolysis in the presence of β-galactosidase, resulting in a significant increase in fluorescence. Its unique structure allows for selective binding to certain biomolecules, facilitating distinct pathways in enzymatic reactions. The compound's solubility and stability in aqueous environments enhance its utility in various biochemical assays. | ||||||
Fluorescein 6-Isothiocyanate, Isomer 2, 95% | 18861-78-4 | sc-218501 | 100 mg | $230.00 | ||
Fluorescein 6-Isothiocyanate, Isomer 2, is a vibrant fluorescent dye that emits light in the 450-495 nm range, characterized by its isothiocyanate functional group. This compound exhibits strong reactivity towards nucleophiles, enabling covalent bonding with amines and thiols, which enhances its utility in labeling studies. Its high solubility in organic solvents and stability under various conditions make it an excellent choice for probing molecular interactions and tracking dynamic processes in complex systems. | ||||||