2020
DOI: 10.20546/ijcmas.2020.904.308
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Morphological and Molecular Characterization of Gastrointestinal Nematodes in Sheep

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(1 citation statement)
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“…Conventional PCR targeting the internal transcribed spacer 2 gene with genus-specific primer pairs ( Table-1 ) [ 27 , 28 ] was used to detect resistant nematodes, namely, Haemonchus spp., Oesophagostomum spp., Trichostrongylus spp., and Teladorsagia spp. The PCR assays were conducted in a 25 μL reaction volume, using 12.5 μL HotStar Taq PCR (Qiagen, Valencia, CA) master-mix, 8.5 μL double distilled water, 1 μL forward primer, 1 μL of reverse primer, and 2 μL DNA template.…”
Section: Methodsmentioning
confidence: 99%
“…Conventional PCR targeting the internal transcribed spacer 2 gene with genus-specific primer pairs ( Table-1 ) [ 27 , 28 ] was used to detect resistant nematodes, namely, Haemonchus spp., Oesophagostomum spp., Trichostrongylus spp., and Teladorsagia spp. The PCR assays were conducted in a 25 μL reaction volume, using 12.5 μL HotStar Taq PCR (Qiagen, Valencia, CA) master-mix, 8.5 μL double distilled water, 1 μL forward primer, 1 μL of reverse primer, and 2 μL DNA template.…”
Section: Methodsmentioning
confidence: 99%