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AP-dC G-Clamp (Aminoethyl-Phenoxazine-dC (AP-dC))


Code : [AP-dC]

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Modification : AP-dC

Catalog Reference Number
Modification Code
5 Prime
3 Prime
Molecular Weight (mw)
Extinction Coeficient (ec)
Technical Info (pdf)
Absorbance MAX
Emission MAX
Absorbance EC

Duplex Stability

Catalog NoScalePrice
26-6920-0550 nmol$497.00
26-6920-02200 nmol$497.00
26-6920-011 umol$969.00
26-6920-032 umol$969.00
26-6920-1010 umol$5,167.00
26-6920-1515 umol$6,458.00
Discounts are available for AP-dC!
Modification* Discount Price Structure
1 site/order List price
2 sites/order 10% discount
3 sites/order 20% discount
4 sites/order 30% discount
5-9 sites/order 50% discount
10+ sites/order 60% discount
*Exceptions apply

Aminoethyl-Phenoxazine-deoxycytosine (AP-dC), sometimes referred to as G-clamp, pairs with dG, and when substituted for dC in an oligonucleotide, is able to form both Watson-Crick and Hoogsteen hydrogen bonds with the guanine base. A total of four hydrogen bonds form between AP-dC and dG: the usual three Watson-Crick hydrogen bonds and a Hoogsteen hydrogen bond between the protonated amine of AP-dCs aminoethyl side-chain and the O6 position of the dG. As a result, an AP-dC:dG base pair significantly increases the stability of the resulting duplex relative to the comparable unmodified form. The increase in stability can be quite dramatic; in one study, a single incorporation of AP-dC in a 10-mer polypyrimidine oligonucleotide raised the Tm of the corresponding duplex by 18 degC over a control duplex containing 5-Me-dC at the same position (1). Moreover, the additional, specific presence of the Hoogsteen hydrogen bond leads to high specificity of AP-dC for dG over the other three bases (1). Thus, AP-dC may be useful in any application in which the ability to discriminate dG in a target is necessary.

Flanagan and co-workers tested AP-dC for its utility in anti-sense oligos. Based on studies of AP-dC-modified anti-sense oligos for sequence-context dependence, activity mismatch, sensitivity, RNAse-H cleavage, and hybridization kinetics, they concluded that AP-dC is a very potent, mis-match sensitive analog for dC, with high potential for improving the potency of anti-sense oligonucleotides (2). In another study, oligos containing one AP-dC at the 3-end confer resistance to 3-exonuclease digestion (3).

AP-dC is an excellent choice of modification whenever a large increase in duplex stability and/or specificity for dG in a target is required.

1. Lin, K.Y.; Matteucci, M.D. A cytosine analogue capable of clamp-like binding to a guanine in helical nucleic acids. J. Am. Chem. Soc. (1998), 120: 8531-8532.
2. Flanagan, W.M.; Wolf, J.J.; Olson, P.; Grant, D.; Kuei-Ying, L.; Wagner, R.W.; Matteucci, M.D. A cytosine analog that confers enhanced potency to antisense oligonucleotides.Proc. Natl. Acad. Sci. (USA) (1999), 96: 3513-3518.
3. Maier, M.A.; Leeds, J.M.; Balow, G.; Springer, R.H.; Bharadwaj, R.; Manoharan, M. Nuclease resistance of oligonucleotides containing the tricyclic cytosine analogues phenoxazine and 9-(2-aminoethoxy)-phenoxazine (G-clamp) and origins of their nuclease resistance properties.Biochem. (2002), 41: 1323-1327.
- AP-dC G-Clamp (Aminoethyl-Phenoxazine-dC (AP-dC))

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