Table 1.
Sequences of the primers used in this study
Peptides | Primer sequences (5’→3’) | Position | Size of amplicon |
---|---|---|---|
tM-His6 |
F: ATACATATGAGCATTCGGTTGTGGCG |
295–678 |
384bp |
R: CGCCTCGAGGACTAAATGAAGCACT | |||
F: TAAGGATCCAGCATTCGGTTGTGGCGCAG | |||
GST-tM |
R: CGGCTCGAGGACTAAATGAAGCACTTTCTCAC |
295–678 |
384bp |
F: TATCATATGAGCATTCGGTTGTGG | |||
M1 |
R: TATCTCGAGTACGCCAGTAGCAAC |
295–480 |
186bp |
F: GCGCATATGCTCACTACTTCTGTGAT | |||
M2 |
R: GCGCTCGAGATAGACAATTGTTGTAG |
358–540 |
183bp |
F: GCACATATGGTACAGGTAAGTCAAT | |||
M3 |
R: CTACTCGAGGACTAAATGAAGCACT |
478–678 |
201bp |
F: gatccGTACAGGTAAGTCAATTACCTAATTTCGTCACAGTCGCCA | |||
M4 |
AGGCCACTACAACAATTGTCTATGGACGTGTTtaac |
478-549 |
72bp |
R: tcgagttaAACACGTCCATAGACAATTGTTGTAGTGGCCTTGGCGA | |||
CTGTGACGAAATTAGGTAATTGACTTACCTGTACg | |||
F: gatccGGACGTGTTGGTCGTTCAGTCAATGCTTCATCTGGCACTG | |||
M5 |
GTTGGGCTTTCTATGTCCGGtaac |
541–600 |
60bp |
R: tcgagttaCCGGACATAGAAAGCCCAACCAGTGCCAGATGAAGCA | |||
TTGACTGAACGACCAACACGTCCg | |||
M6 |
F: gatccTCAGCTGTGAGTAATCCGAGTGCGGTTCTCACAGATtaac |
592–627 |
36bp |
R: tcgagttaCACAGCTGAGTAGTCGCCGTGTTTTGACCGGACATAg | |||
M7 |
F: gatccTCAGCTGTGAGTAATCCGAGTGCGGTTCTCACAGATtaac |
619–654 |
36bp |
R: tcgagttaATCTGTGAGAACCGCACTCGGATTACTCACAGCTGAg F: gatccCTCACAGATAGTGAGAAAGTGCTTCATTTAGTCtaac | |||
M8 |
R: tcgagttaGACTAAATGAAGCACTTTCTCACTATCTGTGAGg |
646–678 |
33bp |
M9 |
F: gatccGGACGTGTTGGTCGTTCAGTCAATtaac |
541–564 |
24bp |
R: tcgagttaATTGACTGAACGACCAACACGTCCg | |||
M10 |
F: gatccCGTTCAGTCAATGCTTCATCTGGCtaac |
553–576 |
24bp |
R: tcgagttaATTGACTGAACGACCAACACGTCCg | |||
M11 |
F: gatccGCTTCATCTGGCACTGGTTGGGCTtaac |
565–588 |
24bp |
R: tcgagttaAGCCCAACCAGTGCCAGATGAAGCg | |||
M12 |
F: gatccACTGGTTGGGCTTTCTATGTCCGGtaac |
577–600 |
24bp |
R: tcgagttaCCGGACATAGAAAGCCCAACCAGTg | |||
M13 |
F: gatccGGTTGGGCTTTCTATGTCCGGtaac |
580–600 |
21bp |
R: tcgagttaCCGGACATAGAAAGCCCAACCg | |||
M14 |
F: gatccTGGGCTTTCTATGTCCGGtaac |
583–600 |
18bp |
R: tcgagttaCCGGACATAGAAAGCCCAg | |||
F003A gatccGCTTTCTATGTCCGGtaac | |||
M15 |
R: tcgagttaCCGGACATAGAAAGCg |
586–600 |
15bp |
R: tcgagttaGACATAGAAAGCCCAg | |||
M16 |
F: gatccTGGGCTTTCTATtaac |
583–597 |
15bp |
R: tcgagttaGACATAGAAAGCCCAg | |||
M17 | F: gatccTGGGCTTTCTATtaac |
583–594 | 12bp |
R: tcgagttaATAGAAAGCCCAg |
The introduced restriction enzyme sites (NdeI and XhoI or BamHI and XhoI) are underlined. At the 5’ and 3’ terminal of each forward strand there is a sequence “gatcc” and “taac” (in italics), respectively. At the 3’ and 5’ terminal of each reverse strand there is a sequence “g” and “tcgagtta” (in italics), respectively. When the forward and reverse oligonucleotides annealed they form a cohesive BamHI site or NdeI at the 5’ terminus and a cohesive XhoI site at the 3’ terminus. The bases “taa” and “tta” (in bold) were introduced into each pair of oligonucleotides to form a stop codon.