Benzoxadiazoles

Apexbio Technology LLC NBD-F 29270-56-2 50mg

NBD-F (29270-56-2) is a fluorescent derivatization reagent utilized for the detection and quantification of amino acids and low molecular weight amines NBD-F exerts its activity by selectively reacting with primary and secondary amines through its benzofurazan structure forming fluorescent conjugates detectable in biological samples Based on these properties NBD-F holds research potential in biochemical analysis metabolic profiling disease pathology investigation and fluorescent labeling in proteomics and molecular biology

Apexbio Technology LLC NBD-F 29270-56-2 100mg

NBD-F (29270-56-2) is a fluorescent derivatization reagent utilized for the detection and quantification of amino acids and low molecular weight amines NBD-F exerts its activity by selectively reacting with primary and secondary amines through its benzofurazan structure forming fluorescent conjugates detectable in biological samples Based on these properties NBD-F holds research potential in biochemical analysis metabolic profiling disease pathology investigation and fluorescent labeling in proteomics and molecular biology

Apexbio Technology LLC NBD-Cl 10199-89-0 500mg

NBD-Cl (10199-89-0) is a fluorescent labeling reagent that covalently reacts with nucleophilic groups specifically amines and thiols It is designed to derivatize these functional groups enabling detection through the formation of highly fluorescent conjugates NBD-Cl exerts its biological utility primarily through its electrophilic reaction mechanism with free amino and thiol groups in biomolecules No specific experimental model or quantitative activity metric is provided Based on these chemical properties NBD-Cl holds research potential in the labeling and detection of amino acid residues peptides proteins and thiol-containing enzymes as well as in studies of enzyme activities and biomolecular interactions

Apexbio Technology LLC NBD-Cl 10199-89-0 1g

NBD-Cl (10199-89-0) is a fluorescent labeling reagent that covalently reacts with nucleophilic groups specifically amines and thiols It is designed to derivatize these functional groups enabling detection through the formation of highly fluorescent conjugates NBD-Cl exerts its biological utility primarily through its electrophilic reaction mechanism with free amino and thiol groups in biomolecules No specific experimental model or quantitative activity metric is provided Based on these chemical properties NBD-Cl holds research potential in the labeling and detection of amino acid residues peptides proteins and thiol-containing enzymes as well as in studies of enzyme activities and biomolecular interactions