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. 2017 Dec 1;18:927. doi: 10.1186/s12864-017-4311-4

Table 9.

Primers used in this study

Primers 5′ to 3′ sequencea Use
XIS1_460109ApaUpF NNNNNNGGGCCCCAGGATATGCCATTCAGC Mutant construction
XIS1_460109BamUpR NNNNNNGGATCCCAATGACATCAGGCACAC Mutant construction
XIS1_460109BamDnF NNNNNNGGATCCGAACCATCGCAGATTGAG Mutant construction
XIS1_460109XbaDnR NNNNNNTCTAGAGCCCAATCGCTTCATATC Mutant construction
XIS1_460115ApaUpF NNNNNNGGGCCCGAATCGCCCTGGATTATG Mutant construction
XIS1_460115BamUpR NNNNNNGGATCCCCCTCTGGCTGATAATAG Mutant construction
XIS1_460115BamDnF NNNNNNGGATCCCTCAGGCTCGATTATTGG Mutant construction
XIS1_460115XbaDnR NNNNNNTCTAGACTGAATGTACTCCTGCTG Mutant construction
NilBF NNNCATATGAGGAAAACGCCACATTCCGG Confirmation PCR
NilBR NNNGGGCCCTTGCATGGTTTGGTTG Confirmation PCR
M13F (−20) GTAAAACGACGGCCAG Sequencing PCR
M13R CAGGAAACAGCTATGAC Sequencing PCR

aN represents A, T, G or C. Engineered restriction enzyme sites are underlined