Items 21 to 27 of 27 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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CruzFluor sm 4 acid | sc-362591 | 10 mg | $195.00 | |||
CruzFluor sm™ 4 acid is a specialized fluorescent compound exhibiting emission in the 590-620 nm range. Its unique structure enables strong interactions with polar solvents, enhancing its solubility and reactivity. The acid's distinctive electrophilic nature allows for rapid acylation reactions, making it a versatile tool for modifying biomolecules. Its exceptional photostability and high quantum yield contribute to reliable performance in various analytical applications, ensuring consistent results in fluorescence assays. | ||||||
CruzFluor sm™ 4 amine | sc-362592 | 1 mg | $195.00 | |||
CruzFluor sm™ 4 amine is a specialized fluorescent compound that emits light in the 590-620 nm range. Its unique amine functional group facilitates strong hydrogen bonding interactions, enhancing its affinity for various substrates. This compound exhibits remarkable stability under diverse conditions, allowing for consistent fluorescence. Additionally, its ability to participate in nucleophilic reactions broadens its applicability in synthetic pathways, making it a valuable asset in research settings. | ||||||
CruzFluor sm™ 4 maleimide | sc-362593 | 1 mg | $195.00 | |||
CruzFluor sm™ 4 maleimide is a distinctive fluorescent compound characterized by its emission in the 590-620 nm range. Its maleimide group enables selective thiol-reactivity, promoting efficient conjugation with biomolecules. This compound demonstrates exceptional photostability, ensuring reliable fluorescence over extended periods. Furthermore, its unique electronic structure allows for rapid reaction kinetics, making it an intriguing choice for exploring molecular interactions in various experimental contexts. | ||||||
CruzFluor sm™ 4 succinimidyl ester | sc-362595 | 5 mg | $195.00 | |||
CruzFluor sm™ 4 succinimidyl ester is a specialized fluorescent dye that emits light in the 590-620 nm range. Its succinimidyl ester functionality facilitates efficient amine coupling, enhancing specificity in labeling applications. The compound exhibits remarkable stability under various conditions, allowing for consistent performance in diverse environments. Additionally, its unique reactivity profile enables rapid conjugation, making it a versatile tool for probing complex molecular interactions. | ||||||
3,3′-Dipropylthiacarbocyanine iodide | 53336-12-2 | sc-209689 | 250 mg | $102.00 | ||
3,3'-Dipropylthiacarbocyanine iodide is a vibrant fluorescent dye characterized by its emission spectrum in the 590-620 nm range. This compound features a unique thiacarbocyanine structure that enhances its photostability and allows for strong interactions with biomolecules. Its distinct electronic properties facilitate efficient energy transfer processes, making it suitable for studying dynamic molecular environments. The dye's robust nature ensures reliable performance across a variety of experimental conditions. | ||||||
6-Carboxy-X-rhodamine N-succinimidyl ester | 216699-36-4 | sc-214364 | 5 mg | $266.00 | ||
6-Carboxy-X-rhodamine N-succinimidyl ester is a highly versatile fluorescent dye known for its emission in the 590-620 nm range. This compound exhibits a reactive N-succinimidyl ester group, enabling efficient conjugation to amine-containing molecules. Its carboxylic acid moiety enhances solubility in aqueous environments, while the rhodamine core contributes to its exceptional brightness and photostability. The dye's unique structure allows for specific interactions with target molecules, facilitating detailed studies of molecular dynamics. | ||||||
Propidium iodide solution | 25535-16-4 | sc-477277 | 1 ml | $130.00 | 2 | |
Propidium iodide solution is a potent fluorescent intercalator that emits light in the 590-620 nm range. Its unique ability to penetrate compromised cell membranes allows it to bind to nucleic acids, resulting in a strong fluorescence signal. This compound exhibits high affinity for double-stranded DNA, leading to enhanced brightness upon binding. Its stability and distinct spectral properties make it an effective tool for studying cellular integrity and nucleic acid interactions in various experimental settings. |