Table 2.
Primers
cDNA primers for cloning of UBE2T into S91-IRES-NEO | |
5′ NotI | CATGCGGCCGCATGCAGAGAGCTTCA |
3′ BamH I | GTAGGATCCCTAAACATCAGGATG |
cDNA primers | |
1F | AGTCAGAGGTCGCGCAGGCGCTG |
1R | CCCTCACAACGCAGCAA |
2F | TGCATCCCAGGCAGCTCTTA |
2R | TAGAAGGAACCACACACAGTTC |
3R | CATAAGGTGTGTTGGCTCCACCTA |
4R | CATCCAGACAAATCCTTCCAGCAG |
5R | TGGGTTCTGACATGAGCAGCTGAA |
6F | CAAGAATGCCAGACAGTGGACAGA |
6R | CTTGAGGAAGGCTGGCTTATTA |
7R | GGTAGGCAACTTAGATCACCTTGGCA |
Genomic primers for the duplicationa | |
ivs5F | CCTCTGCAACACATATCCTACC |
ivs1R | CCTCTGTGCGTCTACATCTATTT |
e7R | TCTATGCCTACTAGCTGACTGG |
Genomic primers for the deletiona | |
1_7F | GCTTCTTTCCCGGTGGATTA |
1_7R | CCCAGACACACATTCAGGATAAA |
ivs1R | AAACTCATGCTTCAGCCACACTGC |
Primers for NMD detectiona | |
Exon 1 | tgtaaaacgacggccagtAGTCAGAGGTCG CGCAGGCGCTGb |
duplication-specific | gcctgggatgcActtttgtttctgc |
aAll primers shown as 5′ to 3′, F = forward, R = reverse.
bContains the M13 forward binding site (small letters).
cUnderlined A indicates the site of the junction in cDNA.