Items 61 to 70 of 83 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4,7-Dioxaoctylenediamine N-[(Cyanine 3) Monofunctional Hexanoic Acid]-N′-[2-fluoro-4′-phosphophenylacetic Acid] Diamide | sc-223673 | 500 µg | $380.00 | |||
4,7-Dioxaoctylenediamine N-[(Cyanine 3) Monofunctional Hexanoic Acid]-N'-[2-fluoro-4'-phosphophenylacetic Acid] Diamide showcases unique molecular interactions that enhance its affinity for specific protein targets. Its dual functional groups facilitate robust binding through electrostatic and hydrophobic interactions, promoting stability in complex environments. The compound's distinct reactivity allows for selective conjugation, enabling precise tracking of biomolecular pathways and interactions in various assays. | ||||||
Ethylenediamine N-[(Cyanine 3) Monofunctional Hexanoic Acid]-N′-[3-difluoromethyl-4-phosphoanilinamidosuccinic Acid] Diamide | sc-223980 | 500 µg | $305.00 | |||
Ethylenediamine N-[(Cyanine 3) Monofunctional Hexanoic Acid]-N'-[3-difluoromethyl-4-phosphoanilinamidosuccinic Acid] Diamide exhibits remarkable specificity in protein and antibody interactions. Its unique structural design incorporates multiple functional moieties that enable strong non-covalent binding, enhancing selectivity. The compound's ability to modulate conformational dynamics allows for effective engagement with target biomolecules, facilitating detailed studies of cellular mechanisms and signaling pathways. | ||||||
CruzFluor™ 350 succinimidyl ester | sc-362615 | 1 mg | $114.00 | |||
CruzFluor™ 350 succinimidyl ester is a highly reactive compound that facilitates efficient conjugation with proteins and antibodies through its succinimidyl ester functionality. This ester undergoes rapid hydrolysis in aqueous environments, releasing reactive intermediates that form stable amide bonds with primary amines. Its unique fluorophore properties enable enhanced fluorescence, making it ideal for sensitive detection and visualization in complex biological systems. The compound's distinct spectral characteristics allow for multiplexing in assays, providing versatility in experimental design. | ||||||
CruzFluor™ 700 succinimidyl ester | sc-362622 | 1 mg | $195.00 | |||
CruzFluor™ 700 succinimidyl ester is a potent labeling agent that exhibits exceptional reactivity towards nucleophilic sites on proteins and antibodies. Its unique structure promotes rapid conjugation, leading to the formation of stable amide bonds. The compound's advanced fluorophore characteristics provide high quantum yield and photostability, enabling precise tracking in dynamic biological environments. Additionally, its distinct emission spectrum allows for effective multiplexing, enhancing experimental flexibility. | ||||||
CruzFluor™ 750 succinimidyl ester | sc-362623 | 1 mg | $195.00 | |||
CruzFluor™ 750 succinimidyl ester is a highly reactive labeling reagent designed for efficient conjugation with proteins and antibodies. Its unique succinimidyl ester moiety facilitates rapid formation of covalent bonds with primary amines, ensuring robust and stable conjugates. The compound's superior fluorescence properties, including enhanced brightness and a distinct emission profile, enable sensitive detection and quantification in complex biological assays. Its optimized spectral characteristics support diverse experimental applications, making it a versatile tool in biochemical research. | ||||||
Chromeo™ 494 alkyne | sc-364700 | 1 mg | $286.00 | |||
Chromeo™ 494 alkyne is a specialized chemical that exhibits remarkable reactivity through its alkyne functional group, enabling selective click chemistry with azide-containing biomolecules. This compound facilitates precise labeling and tracking of proteins and antibodies, enhancing visualization in various assays. Its unique electronic properties contribute to efficient energy transfer, making it ideal for applications requiring high sensitivity and specificity in molecular interactions. | ||||||
Chromeo™ 505 NHS-ester | sc-364706 | 1 mg | $273.00 | |||
Chromeo™ 505 NHS-ester is a highly reactive compound designed for efficient conjugation with amine-containing biomolecules, such as proteins and antibodies. Its NHS-ester functionality promotes rapid and stable formation of amide bonds, ensuring robust labeling. The compound's unique steric and electronic characteristics enhance its solubility and reactivity, allowing for precise modifications in complex biological systems. This specificity aids in elucidating molecular pathways and interactions. | ||||||
Chromeo™ 546 NHS-ester | sc-364710 | 1 mg | $275.00 | |||
Chromeo™ 546 NHS-ester is an advanced reagent that facilitates targeted conjugation with amine-rich biomolecules, including proteins and antibodies. Its NHS-ester group enables swift and efficient amide bond formation, optimizing reaction kinetics. The compound's distinctive steric properties and electronic configuration enhance its reactivity, allowing for selective modifications. This specificity is crucial for studying intricate molecular interactions and pathways in diverse biological contexts. | ||||||
Chromeo™ 642 alkyne | sc-364714 | 1 mg | $275.00 | |||
Chromeo™ 642 alkyne is a specialized reagent designed for precise labeling and modification of biomolecules, particularly proteins and antibodies. Its unique alkyne functionality enables click chemistry reactions, promoting rapid and selective conjugation with azide-containing partners. This compound exhibits remarkable stability under physiological conditions, ensuring reliable performance in complex biological systems. Its distinct reactivity profile allows for the exploration of intricate molecular dynamics and interactions, making it a valuable tool in biochemical research. | ||||||
Chromeo™ 642 NHS-ester | sc-364716 | 1 mg | $287.00 | |||
Chromeo™ 642 NHS-ester is a versatile reagent tailored for the targeted modification of proteins and antibodies. Its NHS-ester functionality facilitates efficient amine coupling, enabling the formation of stable covalent bonds with primary amines. This compound exhibits a rapid reaction rate, enhancing the efficiency of conjugation processes. Additionally, its hydrophilic nature improves solubility in aqueous environments, making it ideal for diverse biochemical applications. | ||||||