Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui
Haplorchis taichui specific primers were designed using a high annealing temperature random amplified polymorphic DNA (HAT-RAPD) PCR method and 18 arbitrary primers (Operon Technologies) to generate polymorphic DNA profiles for 13 different parasites. The H. taichui specific fragment was screened. A...
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th-cmuir.6653943832-598012018-09-10T03:21:41Z Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui Pheravut Wongsawad Chalobol Wongsawad Medicine Haplorchis taichui specific primers were designed using a high annealing temperature random amplified polymorphic DNA (HAT-RAPD) PCR method and 18 arbitrary primers (Operon Technologies) to generate polymorphic DNA profiles for 13 different parasites. The H. taichui specific fragment was screened. A 256 bp HAT-RAPD marker generated from OPP-11 primer specific for H. taichui was cloned and sequenced. From the sequence data, specific primers were designed that generated a 256 bp amplicon. The minimum DNA template needed for PCR detection was 10 fg. The successful development of the H. taichui specific DNA-based detection will be beneficial in management and epidemiological control programs. 2018-09-10T03:21:41Z 2018-09-10T03:21:41Z 2009-09-01 Journal 01251562 2-s2.0-70349789724 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349789724&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59801 |
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Medicine Pheravut Wongsawad Chalobol Wongsawad Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui |
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Haplorchis taichui specific primers were designed using a high annealing temperature random amplified polymorphic DNA (HAT-RAPD) PCR method and 18 arbitrary primers (Operon Technologies) to generate polymorphic DNA profiles for 13 different parasites. The H. taichui specific fragment was screened. A 256 bp HAT-RAPD marker generated from OPP-11 primer specific for H. taichui was cloned and sequenced. From the sequence data, specific primers were designed that generated a 256 bp amplicon. The minimum DNA template needed for PCR detection was 10 fg. The successful development of the H. taichui specific DNA-based detection will be beneficial in management and epidemiological control programs. |
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Pheravut Wongsawad Chalobol Wongsawad |
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Pheravut Wongsawad Chalobol Wongsawad |
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Pheravut Wongsawad |
title |
Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui |
title_short |
Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui |
title_full |
Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui |
title_fullStr |
Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui |
title_full_unstemmed |
Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui |
title_sort |
development of pcr-based diagnosis of minute intestinal fluke, haplorchis taichui |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70349789724&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/59801 |
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