Labeled Nucleotides

Biotin-16-dUTP can be enzymatically incorporated into DNA via nick translation, random priming, or 3′ end terminal labeling. The terminal deoxynucleotidyl transferase (TdT)-mediated biotin-dUTP nick end-labeling (TUNEL) method has been commonly used for apoptosis studies.

Biotin-16-dUTP can be enzymatically incorporated into DNA via nick translation, random priming, or 3′ end terminal labeling. The terminal deoxynucleotidyl transferase (TdT)-mediated biotin-dUTP nick end-labeling (TUNEL) method has been commonly used for apoptosis studies.

Biotin-16-UTP can be enzymatically incorporated into RNA. The number 16 indicates the number of atoms between biotin and UTP.

This product is similar to biotin-11-dUTP (40029) and biotin-16-dUTP (40022) except that it has a longer and water-soluble spacer group, which should facilitate interaction between the biotin group and avidin or streptavidin.

This product is similar to biotin-11-dUTP (40029) and biotin-16-dUTP (40022) except that it has a longer and water-soluble spacer group, which should facilitate interaction between the biotin group and avidin or streptavidin.

This product is similar to biotin-11-UTP (40033) and biotin-16-UTP (40023) except that it has a longer and water soluble spacer group, which should facilitate interaction between the biotin group and avidin or streptavidin.

BrdU (5-Bromo-2′-deoxyuridine) can be incorporated into DNA during cell division and subsequently detected by a BrdU antibody. The probe can be used to study cell-cycle kinetics (1).

BrUTP (5-Bromouridine-5′-triphosphate) can be enzymatically incorporated into RNA and detected with anti-BrdU antibodies.

CF® dye dCTP can be used to synthesize labeled DNA probes for in-situ hybridization, microarray or blotting applications.

DEAC-dUTP (diethylaminocoumarin-dUTP) can be used to synthesize fluorescent DNA probes for in situ hybridization, microarray or blotting techniques. DEAC has absorption at 426 nm and emission at 480 nm.

Digoxigenin-dUTP can be enzymatically incorporated into DNA via nick translation, random priming, or 3′-end terminal labeling to synthesize labeled DNA probes for in-situ hybridization, microarray or blotting techniques.  The digoxigenin labeled probe could be detected by using fluorescent labeled or enzyme labeled anti-digoxigenin antibody.

Fluorescein-12-dUTP can be used to synthesize fluorescent DNA probes.