Biologically Active Small Molecules

A sulfhydryl-reactive biotinylation reagent that forms a reversible disulfide linkage, used to label protein cysteines and other substrates that contain sulfhydryl groups easily linked with target substrates at pH 6.5 to 7.

A sulfhydryl-reactive biotinylation reagent that forms a reversible disulfide linkage, used to label protein cysteines and other substrates that contain sulfhydryl groups easily linked with target substrates at pH 6.5 to 7.

A compound used to attach biotin to primary amines, such as lysines on the surface of proteins, under alkaline conditions (pH~8-9).

A compound used to attach biotin to primary amines, such as lysines on the surface of proteins, under alkaline conditions (pH~8-9).

A compound used to attach biotin to primary amines, such as lysines on the surface of proteins, under alkaline conditions (pH~8-9).

A compound used to attach biotin to primary amines, such as lysines on the surface of proteins, under alkaline conditions (pH~8-9).

A compound used to attach biotin to primary amines, such as those found on lysines on the surface of proteins contains six-atom spacer arm.

A compound used to attach biotin to primary amines, such as those found on lysines on the surface of proteins contains six-atom spacer arm.

A compound used to attach biotin to primary amines, such as those found on lysines on the surface of proteins contains six-atom spacer arm.

A compound used to attach biotin to primary amines, such as those found on lysines on the surface of proteins contains six-atom spacer arm.

A biotinylating reagent that contains two aminohexanoic spacers to increase the efficiency of avidin-binding by alleviating steric hindrance.

A biotinylating reagent that contains two aminohexanoic spacers to increase the efficiency of avidin-binding by alleviating steric hindrance.