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. 2012 Apr 18;12:57. doi: 10.1186/1471-2180-12-57

Table 2.

PCR primers used in this study


Primer Sequence (5'→ 3')

HlyAa GCGGGTACCAGGTAGAGCGGACATCCATTG
HlyBb, c, d GTTTTAGGATCCCCCGGGGGGTTTCACTCTCCTTCTAC
HlyCb, c CCCGGGGGATCCTAAAACCGCTTAACACACACG
HlyDe GCGTCTAGATTCTTCCCCGACAGAATCTGC
NisR F CCCACTAAACAATCGGAGG
NisK Rc GCGGGATCCCAGAAATTAAACCAAACAAAATTTTC
Oepbp3 F CGTGAAACTAAATTTTAGAAAAAAGAAAAAAG
Oepbp3 Rf GCGGCATGCGATTAATTTTCGGTTTGTTCTGATTG

a Nucleotide substitutions to create KpnI site are underlined

b Nucleotide substitutions to create SmaI site are underlined

c Nucleotide substitutions to create BamHI site are in boldface

d Overhang complementary to SOE primer is in italics

e Nucleotide substitutions to create XbaI site are underlined

f Nucleotide substitutions to create SphI site are underlined