Table 1.
Primer | Sequence (5'→3') | Method | Company |
FLJforward | CCCAAGCTTGGGGCGGGGAGATGAACGGCTTC | EGFP-PCR | Genset Oligos |
FLJreverse | CCGGAATTCTCAAGCTGCTTGCCACCCTCCGA | EGFP-PCR | Genset Oligos |
EX1S | AGCACGGAGGAGGACAGCCGCGAA | Sequencing | Genset Oligos |
EX2S | GTAAGGCACCTATATATCTGTGAT | Sequencing | Genset Oligos |
EX2AS | GTGTCGTGCTCGGGAGAATCTCCG | Sequencing | Genset Oligos |
EX3S | GTTGATCTGTTCCAGCTGCAGGTG | Library screening LightCycler Northern probe |
Genset Oligos |
EX3AS | TTCTGCTAACTGGGCCTTATTGAA | Sequencing | Genset Oligos |
EX4AS | TCAAGCTGCTTGCCACCCTCCGA | Library screening LightCycler Northern probe |
Genset Oligos |
3G3TNLSfor | CGAAATAAAAGTAACAGGAAGACAAGT | NLS mutation | TAG Copenhagen |
3G3TNLSrev | ACTTGTCTTCCTGTTACTTTTATTTCG | NLS mutation | TAG Copenhagen |
The table indicates the names and sequences of the primers used in given experiments.