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. 2006 Dec 20;35(3):755–770. doi: 10.1093/nar/gkl1088

Table 1.

Primers used for isolation of RPA32 and RPA70 genes

Orientationa Sequence of primer (5′→3′)b Usage
S TTY RYK VTT GAY GAY GGH ACM GG Partial RPA32
A CTC RTC SAW WGT YGA GTA TAT KHR MCC
S CCG GAG CTC GAG CGC GCT AGC 5′ RPA32
A CACAG GCC TGA CAG ACA AGG C
S GGA ATA CAT GTT GAA GAA CTA GC 3′ RPA32
A GTC GTC GAC ATA TGA TCA AGC TT
S ATG GAT CCA TGT TCT CCA GCT CCC AAT TTG AC RPA32 full-length
A TTG AGT CGA CTC AAG CTT GTT TGT AGT GGG AGT C
S TCA ARR GGA ARY TTG ARR CCT GC Partial RPA70
A CCR WTC ATS WWA GGR CAA GC
S CTT ACG AGC CTG GTT TGA TCA AG 5′ RPA70
A GTC ACA GGC CTG ACA GAC AAG GC
S GGA ATA CAT GTT GAA GAA CTA GC 3′ RPA70
A GAA GGA TTC ACA GAT GTC ACA ACC
S CAT GGA TCC ATG TCG GTG AAT CTC ACG GCG AG RPA70 full-length
A TTG AGT CGA CTT ACT TCC TAC CGA ACT TGG AAA TC

aS, sense; A, antisense.

bThe primers underlined contained BamHI restriction site in the forward primer and SalI in the reverse primer preceded by a stop codon.