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. 2007 May 30;35(12):3907–3917. doi: 10.1093/nar/gkm374

Table 1.

Oligoribonucleotides and PNA used in this study

A: Oligoribonucleotides used as PNA binding target for thermal denaturation experiments
RNA-I-wt: 5′AAAAGAAAAGGGG3′
RNA-I-mut: 5′AAAAGAAAAAGGA3′
RNA-II-wt: 5′AGAAAAGGGGGGA3′
RNA-II-mut: 5′AGAAAAAGAGAGA3′
B: Oligoribonucleotides used as PNA binding target for gel shift assays
RNA-III-wt: 5′UUAAAAGAAAAGGGGGGAU3′
RNA-III-mut: 5′AUAAAAGAAAAAGGAGGAU3′
C: PNAas used in this study
13mer-I PNA: NH2-CCCCTTTTCTTTT-Lys
13mer-II PNA: NH2-TCCCCCCTTTTCT-Lys
13mer-I-Acr PNA: Acr-eg1-CCCCTTTTCTTTT-Lysb
9mer PNA: NH2-TTTTCTTTT-Lys
9mer-Acr PNA: Acr-AEEA-TTTTCTTTT-Lysc
9mer-bis-PNA: NH2-TTTTCTTTT-AEEA-TTTTCTTTT-Lysc
11mer-bis-PNA: NH2-CCTTTTCTTTT-AEEA-TTTTCTTTTCC-Lysc
13mer-scr PNA: NH2-TTTTCCTCTCCCT-Lys
D: ODNs used for RNAse H cleavage
15mer-PPT: 5′ TCTTTTAAAATTGTG3′
15mer-PPT-I: 5′ AATTTTCTTTAATTC3′
15mer-PPT-II: 5′ TTATTCTTTAGTTTG3′

aPNA base sequences are written from N to C terminus.

beg1, 8-amino-3, 6 dioxaoctanoic acid.

cAEEA, 2-(2aminoethoxy) ethoxy acetic acid.