Table 2

Oligonucleotide primers used in this study

PrimerSequence (5′ –> 3′)Application
Pk 150R CTGGCAGGTTATAGAGCTGC 5′ RACE 
Pk 47R GTGCAGACCCGCTGCCTTG 5′ RACE 
Pk 2a-90R TCTCGAACTCCTGACTTCAAG 5′ RACE 
Pk 2a-R-con CAAAGTGCTGGGATTACAGGC 5′ RACE 
Pk ex1-F CCGGGGCCCCGCTGTC 3′ RACE 
Pk 69F CAGCGGGTCTGCACCCTG 3′ RACE 
Pk 110-F TGATCTACTGGCACGTTGTGGG 3′ RACE 
Pk −1070F TATTCAACGCGTACAGCCTGTGATGGGAATGAC Luciferase 
Pk −577F TATTCAACGCGTTTCTCACATTGAACAAATTACCA Luciferase 
Pk −382F TATTCAACGCGTCCCAGGGGTGACAGCGTC Luciferase 
Pk −316F TATTCAACGCGTAGTTTTCTCATCAGTTCAATGG Luciferase 
Pk −240F TATTCAACGCGTGACTGGGGACTGTCCGCA Luciferase 
Pk −136F TATTCAACGCGTGACCCGCAGGGTAGGTCG Luciferase 
Pk +6R TATTCAAAGCTTCTCTAGCTCCAGCGGCGG Luciferase 
Pk P1P2-F TTGAATGAATTAACCGAAAGAAGTAGG PCR-ASP 
Pk P1m-R* CCAAAGTGCTGGGATTACAGACG PCR-ASP 
Pk P2m-R* CCAAAGTGCTGGGATTACAGACA PCR-ASP 
JK ASP-CF GCATGCTGCCATAGGATCATTGC PCR-ASP 
JK ASP-CR GAGCCAGGAGGTGGGTTTGCC PCR-ASP 
Pk i1 2648R ATGACATAGCAAAATGCAAGCA i1-seq 
Pk i1 2145F TGAATTAACCGAAAGAAGTAGG i1-seq, PCR-RFLP 
Pk 2a-240-R CTCGGCTCACTGCACTCTCT PCR-RFLP 
PrimerSequence (5′ –> 3′)Application
Pk 150R CTGGCAGGTTATAGAGCTGC 5′ RACE 
Pk 47R GTGCAGACCCGCTGCCTTG 5′ RACE 
Pk 2a-90R TCTCGAACTCCTGACTTCAAG 5′ RACE 
Pk 2a-R-con CAAAGTGCTGGGATTACAGGC 5′ RACE 
Pk ex1-F CCGGGGCCCCGCTGTC 3′ RACE 
Pk 69F CAGCGGGTCTGCACCCTG 3′ RACE 
Pk 110-F TGATCTACTGGCACGTTGTGGG 3′ RACE 
Pk −1070F TATTCAACGCGTACAGCCTGTGATGGGAATGAC Luciferase 
Pk −577F TATTCAACGCGTTTCTCACATTGAACAAATTACCA Luciferase 
Pk −382F TATTCAACGCGTCCCAGGGGTGACAGCGTC Luciferase 
Pk −316F TATTCAACGCGTAGTTTTCTCATCAGTTCAATGG Luciferase 
Pk −240F TATTCAACGCGTGACTGGGGACTGTCCGCA Luciferase 
Pk −136F TATTCAACGCGTGACCCGCAGGGTAGGTCG Luciferase 
Pk +6R TATTCAAAGCTTCTCTAGCTCCAGCGGCGG Luciferase 
Pk P1P2-F TTGAATGAATTAACCGAAAGAAGTAGG PCR-ASP 
Pk P1m-R* CCAAAGTGCTGGGATTACAGACG PCR-ASP 
Pk P2m-R* CCAAAGTGCTGGGATTACAGACA PCR-ASP 
JK ASP-CF GCATGCTGCCATAGGATCATTGC PCR-ASP 
JK ASP-CR GAGCCAGGAGGTGGGTTTGCC PCR-ASP 
Pk i1 2648R ATGACATAGCAAAATGCAAGCA i1-seq 
Pk i1 2145F TGAATTAACCGAAAGAAGTAGG i1-seq, PCR-RFLP 
Pk 2a-240-R CTCGGCTCACTGCACTCTCT PCR-RFLP 
*

Mutations were introduced in the −3 position in both reverse primers to increase allele specificity.

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