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.6653943832-7202014-08-29T09:02:00Z Hemoglobin E detection using PCR with confronting two-pair primers Intorasoot S. Thongpung R. Tragoolpua K. Chottayaporn M. 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. 2014-08-29T09:02:00Z 2014-08-29T09:02:00Z 2008 Article 01252208 19127788 JMTHB http://www.scopus.com/inward/record.url?eid=2-s2.0-57149086322&partnerID=40&md5=70943db6700e8e93ad07571f3d3ecdbc http://www.ncbi.nlm.nih.gov/pubmed/19127788 http://cmuir.cmu.ac.th/handle/6653943832/720 English |
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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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Article |
author |
Intorasoot S. Thongpung R. Tragoolpua K. Chottayaporn M. |
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Intorasoot S. Thongpung R. Tragoolpua K. Chottayaporn M. Hemoglobin E detection using PCR with confronting two-pair primers |
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Intorasoot S. Thongpung R. Tragoolpua K. Chottayaporn M. |
author_sort |
Intorasoot S. |
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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2014 |
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http://www.scopus.com/inward/record.url?eid=2-s2.0-57149086322&partnerID=40&md5=70943db6700e8e93ad07571f3d3ecdbc http://www.ncbi.nlm.nih.gov/pubmed/19127788 http://cmuir.cmu.ac.th/handle/6653943832/720 |
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