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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Main Authors: Wongsawad P., Wongsawad C.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-70349789724&partnerID=40&md5=2de8ebf2670d6e7ef619db7268ba24ae
http://www.ncbi.nlm.nih.gov/pubmed/19842374
http://cmuir.cmu.ac.th/handle/6653943832/5822
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-58222014-08-30T03:23:30Z Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui Wongsawad P. Wongsawad C. 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. 2014-08-30T03:23:30Z 2014-08-30T03:23:30Z 2009 Article 01251562 19842374 http://www.scopus.com/inward/record.url?eid=2-s2.0-70349789724&partnerID=40&md5=2de8ebf2670d6e7ef619db7268ba24ae http://www.ncbi.nlm.nih.gov/pubmed/19842374 http://cmuir.cmu.ac.th/handle/6653943832/5822 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description 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.
format Article
author Wongsawad P.
Wongsawad C.
spellingShingle Wongsawad P.
Wongsawad C.
Development of PCR-based diagnosis of minute intestinal fluke, Haplorchis taichui
author_facet Wongsawad P.
Wongsawad C.
author_sort Wongsawad P.
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
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-70349789724&partnerID=40&md5=2de8ebf2670d6e7ef619db7268ba24ae
http://www.ncbi.nlm.nih.gov/pubmed/19842374
http://cmuir.cmu.ac.th/handle/6653943832/5822
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