Skip to main content
. 2015 Jun 17;24(18):5093–5108. doi: 10.1093/hmg/ddv227

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.