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. 2017 Jul 27;12(7):e0181864. doi: 10.1371/journal.pone.0181864

Table 1. Oligonucleotide primers used in the study.

Primer Positiona Sequence (5′ to 3′)b Ref.
(for Eh Igls)
EhIgl-S14 40–59 CCCTCGAGGATTATACTGCTGATAAGCT [9, 12]
EhIgl2-S14 40–70 CCCTCGAGGATTATACTGCTGATAAACTCATTAATAACC [7]
EhIgl-S294 880–898 CCCTCGAGACAGAAGAAAATAAATGTA [9, 12]
EhIgl-S603 1807–1827 CCCTCGAGGAAGGACCAAATGCAGAAGAT [9, 12]
EhIgl-AS753 2244–2259 CCCTCGAGTTATAGCCTTTGTTCAGTG [9, 12]
EhIgl-AS1088c 3247–3264 CCCTCGAGTTAAATGCCTTTAGCTCCATT [9, 12]
(for Ed Igls)
EdIgl-S14 40–59 CCCTCGAGGAGTACAAAGCTGATAAACT [8]
EdIgl2-S14 40–63 CCCTCGAGGATTACAAAGCTGATAAACTCATC [8]
EdIgl-S604 1810–1830 CCCTCGAGGAAGGACCAAATGAAGAAGAT *
EdIgl-AS1097c 3274–3291 CCCTCGAGTTAAATTCCTTTACTTCCATT [8]

a Nucleic acid numbering is based on the E. histolytica Igl1 and Igl2 gene sequences (AF337950 and XM_647302) and E. dispar Igl1 and Igl2 gene sequences (AB287423 and AB287424).

b Nucleotides added for cloning and translation termination are underlined.

c EhIgl-AS1088 and EdIgl-AS1097 are common for EhIgl2 and EdIgl2 respectively.

* This study.