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. 2015 May 15;57(9):801–813. doi: 10.1007/s12033-015-9873-2

Table 1.

Oligonucleotide primers used in the work—a summary

Oligonucleotide name Sequence Remarks
Syncytin_out_F 5′-TGCCCCATCGTATAGGAGTC-3′ For the cloning procedure, PNA-mediated PCR and megaprimer mutagenesis
Syncytin_out_R 5′-CGGGTGAGTTGGGAGATTAC-3′ For the cloning procedure
sync1_REV/-2*) 5′-ATTCCACCCCCATCAGACATA-3′ *) Reverse primers used in the PNA-mediated PCR clamping together with Syncytin_out_F as forward primer
sync1_REV/-1*) 5′-AATTCCACCCCCATCAGACAT-3′ As above
sync1_REV/0*) 5′-GAATTCCACCCCCATCAGACA-3′ As above
Mutagenic MRSV 5′-CAGACATACTGGTATGGGTGAAGT-3′ For use in the megaprimer mutagenesis technique
PNA ERVWE1 N′-TACCAGTTTGGGTG-C′ For the PNA-mediated PCR clamping of ERVWE1
PNA ERVWE1-T N’-TACCAGTTTGGGTGA-C’ For the PNA-mediated PCR clamping of ERVWE1
MSRV Probe FAM 5′-CTTACTTCACCCATACCAGTATGTCTGATG- 3′ BHQ1 For the quantitation of MSRV sequences by means of QPCR