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. 2007 Sep 5;2(9):e828. doi: 10.1371/journal.pone.0000828

Table 1. Oligodeoxynucleotides used in subcloning, PCR, UV cross-linking and mutagenesis studies.

Name Sequence Experiment
pG3 forward 5′–CTGAGCTATTCCAGAAGTAGTGAGG-3′ Transfection analysis
pG3 reverse 5′-GCAAGAAGGGAGGGCGAGTTCAGCG-3′ Transfection analysis
WT forward 5′-AGAAACTGATCAGCTTGAAGAGGAAAAG-3′ MiniFosB gene
WT reverse 5′-GTACGAAGGGCTAACAACGG-3′ MiniFosB gene
5′ forward 5′-GCATGCTAATACGACTCACTATAGGGTGAGAGA TTTGCCAGG-3′ UV cross-linking
5′ reverse 5′-TCTTCCTTAGCGGATGTTG-3′ UV cross-linking
Middle forward 5′-GCATGCTAATACGACTCACTATAGGGCGGCTTCGGCTGGCTG-3′ UV cross-linking
Middle reverse 5′-CTGCTCTGGAAGGGCAGG-3′ UV cross-linking
3′ forward 5′-GCATGCTAATACGACTCACTATAGGGCCGAGACGCACCCCCCA-3′ UV cross-linking
3′ reverse 5′-TGTGTGTAAAGAGAGAAGCCGTCAG-3′ UV cross-linking
ISS/T6 forward 5′-CACCCCCCAACCTGACGGCTTTTTTCTTTACACACAGTGAAGTTC-3′ ISS/T6 mutagenesis
ISS/T6 reverse 5′-GAACTTCACTGTGTGTAAAGAAAAAAGCCGTCAGGTTGGGGGGTG-3′ ISS/T6 mutagenesis
Exon 4 forward 5′-AAAAGGCAGAGCTGGAGTCG-3′ PCR of splice products
Exon 5 reverse 5′-GTACGAAGGGCTAACAACGG-3′ PCR of splice products
Intron 4 forward 5′GCATGCTAATACGACTCACTATAGGGCGGCTTCGGCTGGCTG-3′ PCR of splice products