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Oligo Modifications List | Oligo Modifications Reference Category
Modification : L-RNA Bases
Reference Catalog Number 27-6940
Category Others
Modification Code L-rN
5 Prime Y
3 Prime Y
Internal Y
Molecular Weight (mw) 330.23
Extinction Coeficient (ec) 10.67
Technical Info (pdf) PS27-6940.pdf
Catalog NoScalePrice
27-6940-0550 nmol$187.00
27-6940-02200 nmol$187.00
27-6940-011 umol$336.60
27-6940-032 umol$504.90
27-6940-1010 umol$1,992.80
27-6940-1515 umol$2,266.00

Discounts are available for L-RNA Bases!
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

Related Modifications
L-RNA is the left-turning and mirror image version of natural RNA, as opposed to the naturally occurring right-turning version called D-RNA. L-RNA is more stable than D-RNA to enzymatic degradation by certain nucleases (1). Since the two enantiomers are identical in structure other than their chiral differences, their intrinsic physical properties are generally equal to each other. This includes duplex stability, solubility, and selectivity as D-RNA but form a left-helical double-helix. Because of its chiral difference, L-RNA does not bind to its naturally occurring D-RNA counterpart.

One important aspect of L-RNA is that it is poor at hybridizing to D-RNA (2). This confers multiple uses, one being that the incorporation of L-RNA into the stem of a molecular beacon as it allows stem invasion to be avoided (3). Other areas that it can play an important role in would be zip-code microarrays (2) and as molecular tags for PCR (4). When used in nanocarriers, L-DNA has greater cellular uptake as well as greater serum stability. It is good for also reducing interaction between aptamers and nanocarrier skeletons (5).

Gene Link synthesizes L-RNA oligos with any combination of D-RNA bases including fluorescent dyes and all other available modifications and chimeric bases.

L-DNA Applications


1) Damha M.J., Giannaris P.A., Marfey P. Antisense L/D-oligonucleotide chimeras: nuclease stability, base-pairing properties, and activity at directing ribonuclease H. Biochemistry. 1994;33:7877?7885.<
2) Utilising the left-helical conformation of L-DNA for analysing different marker types on a single universal microarray platform Nicole C. Hauser, Rafael Martinez, Anette Jacob, Steffen Rupp, J”rg D. Hoheisel, Stefan Matysiak Nucleic Acids Res. 2006 October; 34(18): 5101-5111. Published online 2006 September 20. doi:˙10.1093/nar/gkl671
3) Superior structure stability and selectivity of hairpin nucleic acid probes with an L-DNA stem. Youngmi Kim, Chaoyong James Yang, Weihong Tan Nucleic Acids Res. 2007 December; 35(21): 7279?7287. Published online 2007 October 24. doi:˙10.1093/nar/gkm771
4) Hayashi G., Hagihara M., Nakatani K. Application of L-DNA as a molecular tag. Nucleic Acids Symp. Ser. 2005;49:261?262
5) Utilizing the bioorthogonal base-pairing system of L-DNA to design ideal DNA nanocarriers for enhanced delivery of nucleic acid cargos Kyoung-Ran Kim, Taemin Lee, Byeong-Su Kim and Dae-Ro Ahn. Chem. Sci., 2014,5, 1533-1537

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