Date published: 2026-4-1

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NBDs

Santa Cruz Biotechnology now offers a broad range of NBDs for use in various applications. NBDs, or nitrobenzoxadiazole derivatives, are a class of fluorescent probes widely utilized in the scientific community for their unique properties. These compounds are particularly valued for their high sensitivity and specificity in detecting and visualizing various biological molecules and processes. In research laboratories, NBDs are often used as markers in biochemical assays to track and measure interactions within cells and between proteins, lipids, and other biomolecules. The versatility of NBDs allows them to be incorporated into different molecular structures, enabling researchers to study complex biological systems with greater accuracy and detail. Their fluorescent nature also makes them ideal for applications in imaging and microscopy, providing vital insights into cellular dynamics and molecular mechanisms. As such, NBDs have become indispensable tools in fields such as molecular biology, biochemistry, and biophysics, aiding in the advancement of scientific knowledge and technological innovation. View detailed information on our available NBDs by clicking on the product name.

Items 31 to 32 of 32 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

N-Dodecanoyl-NBD-D-erythro-dihydrosphingosine

474943-05-0sc-364764
100 µg
$300.00
(0)

N-Dodecanoyl-NBD-D-erythro-dihydrosphingosine is characterized by its unique structural features that facilitate specific molecular interactions. The NBD moiety acts as a fluorescent tag, allowing for real-time monitoring of lipid dynamics. Its dodecanoyl chain enhances hydrophobic interactions, promoting membrane integration. Additionally, the dihydrosphingosine backbone contributes to distinct lipid bilayer properties, influencing phase behavior and stability, which can affect cellular signaling pathways.

4-(2-Aminoethylamino)-7-(N,N-dimethylsulfamoyl)benzofurazan

189373-41-9sc-214197
25 mg
$115.00
(0)

4-(2-Aminoethylamino)-7-(N,N-dimethylsulfamoyl)benzofurazan exhibits intriguing properties due to its unique functional groups. The sulfonamide moiety enhances solubility in polar environments, while the benzofurazan core provides strong electron-withdrawing characteristics, influencing reactivity. This compound can engage in specific hydrogen bonding and π-π stacking interactions, which may alter its kinetics in various chemical reactions, leading to distinct pathways in complex systems.