Hemoglobin E detection using PCR with confronting two-pair primers
Objective: To develop and apply the polymerase chain reaction with confronting two-pair primers (PCR-CTPP) for detection and identification of hemoglobin E (Hb E). Material and Method: Fifty unrelated northern Thais were included in the present study. DNA was extracted from peripheral blood mononucl...
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th-cmuir.6653943832-605732018-09-10T03:45:35Z Hemoglobin E detection using PCR with confronting two-pair primers Sorasak Intorasoot Rachanu Thongpung Khajornsak Tragoolpua Mongkol Chottayaporn Medicine Objective: To develop and apply the polymerase chain reaction with confronting two-pair primers (PCR-CTPP) for detection and identification of hemoglobin E (Hb E). Material and Method: Fifty unrelated northern Thais were included in the present study. DNA was extracted from peripheral blood mononuclear cells and targeted to amplify by PCR-CTPP. The amplified product was analyzed and compared with the reference hemoglobin electrophoresis and polymerase chain reactionrestriction fragment length polymorphism (PCR-RFLP) analysis. Results: The results validated a completely concordant among these three methods consisting of 74%, 24%, and 2% identified as normal, heterozygous, and homozygous Hb E type, respectively. Conclusion: Successful Hb E genotyping by PCR-CTPP was introduced. It allows for confirming and simultaneously detection with other thalassemia mutations. 2018-09-10T03:45:35Z 2018-09-10T03:45:35Z 2008-11-01 Journal 01252208 01252208 2-s2.0-57149086322 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=57149086322&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60573 |
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Medicine Sorasak Intorasoot Rachanu Thongpung Khajornsak Tragoolpua Mongkol Chottayaporn Hemoglobin E detection using PCR with confronting two-pair primers |
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Objective: To develop and apply the polymerase chain reaction with confronting two-pair primers (PCR-CTPP) for detection and identification of hemoglobin E (Hb E). Material and Method: Fifty unrelated northern Thais were included in the present study. DNA was extracted from peripheral blood mononuclear cells and targeted to amplify by PCR-CTPP. The amplified product was analyzed and compared with the reference hemoglobin electrophoresis and polymerase chain reactionrestriction fragment length polymorphism (PCR-RFLP) analysis. Results: The results validated a completely concordant among these three methods consisting of 74%, 24%, and 2% identified as normal, heterozygous, and homozygous Hb E type, respectively. Conclusion: Successful Hb E genotyping by PCR-CTPP was introduced. It allows for confirming and simultaneously detection with other thalassemia mutations. |
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Journal |
author |
Sorasak Intorasoot Rachanu Thongpung Khajornsak Tragoolpua Mongkol Chottayaporn |
author_facet |
Sorasak Intorasoot Rachanu Thongpung Khajornsak Tragoolpua Mongkol Chottayaporn |
author_sort |
Sorasak Intorasoot |
title |
Hemoglobin E detection using PCR with confronting two-pair primers |
title_short |
Hemoglobin E detection using PCR with confronting two-pair primers |
title_full |
Hemoglobin E detection using PCR with confronting two-pair primers |
title_fullStr |
Hemoglobin E detection using PCR with confronting two-pair primers |
title_full_unstemmed |
Hemoglobin E detection using PCR with confronting two-pair primers |
title_sort |
hemoglobin e detection using pcr with confronting two-pair primers |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=57149086322&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60573 |
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