Skip to content Skip to navigation menu

Caged Strand-Breaker II CE-Phosphoramidite

Caged Strand-Breaker II CE-Phosphoramidite

Caged Strand-Breaker II CE-Phosphoramidite, 250 mg, ABI (10 mL / 20 mm Septum)

CAS No.:2089442-43-1

After incorporation into an oligonucleotide, irradiation at 365 nm causes strand cleavage, leaving a phosphate on the 5' end and a hydroxyl residue on the 3' end.
Option 1: Select a Size
Option 2: Select a Bottle Type
Item ID BA0420-B250
TBD
Add to basket to request a quote

Product information

The introduction of nicks in DNA may be accomplished using photolabile nucleotides or nucleotide surrogates, resulting in so-called "caged strand-breaks".(1) Various non-nucleosidic monomers have been developed for this purpose.(2) Caged Strand-Breaker CE-Phosphoramidite is the most advanced example of this strategy, allowing complete removal of the photolabile protecting group from both phosphorylated daughter strands and the avoidance of a second step involving base treatment.2e Further, Caged Strand-Breaker CE-Phosphoramidite II also facilitates implementation of this strategy, but gives rise to daughter strands with a phosphate group on the 5'-terminus and a hydroxyl residue on the 3'-terminus.

Ref:

  1. Reviews: (a) Mayer, G.; Heckel, A. Angew. Chem. Int. Ed. 2006, 45, 4900-4921. (b) Young, D. D.; Deiters, A. Org. Biomol. Chem. 2007, 5, 999-1005. (c) Tang, X. Dmochowski, I. J. Mol. BioSyst. 2007, 3, 100-110.
  2. (a) Urdea, M. S.; Horn, T. US Patent 5,258,506, Nov. 2, 1993. (b) Ordoukhanian, P.; Taylor, J.-S. J. Am. Chem. Soc. 1995, 117, 9570-9571. (c) Zhang, K.; Taylor, J.-S. J. Am. Chem. Soc. 1999, 121, 11579-11580. (d) Ordoukhanian, P.; Taylor, J.-S. Bioconj. Chem. 2000, 11, 94-103. (e) Zhang, K.; Taylor, J.-S. Biochemistry 2001, 40, 153-159. (f) Dell'Aquila, C.; Imbach, J.-L.; Rayner, B. Tetrahedron Lett. 1997, 38, 5289-5292.

Access support

Need some support with placing an order, setting up an account, or finding the right protocol?

Contact us