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. 2019 May 8;35(5):77. doi: 10.1007/s11274-019-2652-7

Table 2.

PCR Primers (5′→3′ direction) used in this study

ID Primers Sequence and description
1 fw_SEA0027

attagacgtcTAGTCGCCGCAGTAGTGATG

Cloning NSI from Synechococcus genome (AatII overhang)

2 rv_SEA0027

aatggatccACCCGGTAGGGATTTCG

Cloning NSI from Synechococcus genome (BamHI overhang)

3 fw_pDF_s_iq_e_t2

CTGGCTTTGCTTCCAGATGT

Cloning of pDF cassette containing Spr/Strr, LacIq, Ptrc, efe variants and two rrnB terminators

4 rv_pDF_s_iq_e_t2_EagI

taaacggccgCTTTCAGCTAGCGTACCA

Cloning of pDF cassette containing Spr/Strr, LacIq, Ptrc, efe variants and two rrnB terminators (Eagl overhang)

5 fw_seq_NSI_7942

TAGTCGCCGCAGTAGTGATG

Sequencing and colony PCR

6 rv_seq_NSI_7942

CTCCAGCAAGCTAGCGATTT

Sequencing and colony PCR

7 75_pUC_Rev

GCTCACTCATTAGGCACCCCAGG

Sequencing and colony PCR

8 rv_seq_NSI_ins

AGGGCCGTGATCTTGTCAT

Sequencing and colony PCR

Complementary regions are shown in capital letters and restriction sites are underlined