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. 2019 Aug 26;26:53. doi: 10.1051/parasite/2019056

Table 1.

The primers used in the characterization of G. duodenalis in the present study.

Gene Primer sequence (5′ – 3′) Fragment length (bp) Annealing temperature (°C) Usage (s) References
SSU rRNA Gia2029: AAGTGTGGTGCAGACGGACTC ~497 55 Specific nested PCR of G. duodenalis [2]
Gia2150c: CTGCTGCCGTCCTTGGATGT
RH11: CATCCGGTCGATCCTGCC ~292 59
RH4: AGTCGAACCCTGATTCTCCGCCCAGG
bg G7: AAGCCCGACGACCTCACCCGCAGTGC ~753 65 Genotyping of G. duodenalis [9]
G759: GAGGCCGCCCTGGATCTTCGAGACGAC
Forward: GAACGAGATCGAGGTCCG ~511 55
Reverse: CTCGACGAGCTTCGTGTT
gdh Ghd1: TTCCGTRTYCAGTACAACTC ~530 50 Genotyping of G. duodenalis [5]
Gdh2: ACCTCGTTCTGRGTGGCGCA
Gdh3: ATGACYGAGCTYCAGAGGCACGT 50
Gdh4: GTGGCGCARGGCATGATGCA
tpi AL3543: AAATIATGCCTGCTCGTCG) ~605 50 Genotyping of G. duodenalis [19]
AL3546: CAAACCTTITCCGCAAACC)
AL3544: CCCTTCATCGGIGGTAACTT) ~530 50
AL3545: GTGGCCACCACICCCGTGCC)