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. 2014 Nov;80(21):6591–6600. doi: 10.1128/AEM.01883-14

TABLE 2.

Oligonucleotides used for PCR amplification of RHD genes

Designation Sequence (5′–3′)a Targeted gene(s)
C095-F GAAGGAGATATATTATGGATAATAATTTCACCATC pahAa
C095-R CGTCGACTTAATAAAAACGGTCAAAATGC AACTG pahAa
C113-F GCTCGAGGAGATATTGTATGAATACCCGTGTCAA pahAb
C113-R CTTATTCTACTTCTGCCTCAA pahAb
C951-F GCATATGATAAATATAGATGATCTGATTGA pahAc2-pahAd2
C341-Rb CTCGAGTTAAAATAAAGTGTTCATGTTGCTATC pahAc2-pahAd2
C763-F GCATATGATGAAGCCAAGCGAGTTGATTGA pahAc4-pahAd4
C569-F GCATATGGTCGATGTAAACAGTCTG pahAc3-pahAd3
C2271-R GCCTACCCAATGGCTGATGCC pahAc3-pahAd3
C451-F1 GAAGGAGATATCATATGAATGAATGGCTGGAGGAG pahAc5-pahAd5
C451-R GTCTAGATCAGAAAAACATATTCAGATTTTTATC pahAc5-pahAd5
C451-F2*c GAAGGAGATATCATATGAAAAACATTAACTATCAGGAAC pahAc5-pahAd5
JCA7-R2* GGCTCGAGATCAGAAAAACATATTCAGA pahAc5-pahAd5
C5241-F GCATATGTTCGATATCAAGAATTTAATCAA pahAc8-pahAd8
C427-R2 CTCGAGTTACAAGATAAACAACAAGTTTTTCCC pahAc8-pahAd8
a

Letters in italics indicate restriction sites for one of the following enzymes: NdeI, SalI, XhoI, or XbaI.

b

This primer was used for the amplification of pahAc4-pahAd4, together with C763-F.

c

Primers used for subcloning pahAc5-pahAd5 in pET15b are indicated by an asterisk (*).