VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000

Factor XIII (FXIII) Val34Leu is the most important polymorphism of the A subunit in factor XIII gene. The aim of the present study was to develop an efficient method based on real time PCR with Fluorescence resonance energy transfer (FRET) detection and melting curve analysis for the detection of...

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Main Authors: Maryam NASER KAMJOO, Ali NAZEMI
Format: Article
Language:English
Published: Rojan GÜMÜŞ 2016-01-01
Series:International Journal of Health Services Research and Policy
Subjects:
Online Access:http://dergipark.gov.tr/ijhsrp/issue/30684/331445
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spelling doaj-f92cb346f3fd4acd8aafc75126e4a2af2021-10-02T12:16:28ZengRojan GÜMÜŞInternational Journal of Health Services Research and Policy2602-34822016-01-0111151910.23884/ijhsrp.2016.1.1.02VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000Maryam NASER KAMJOO0Ali NAZEMI1Islamic Azad University/IRANIslamic Azad University/IRANFactor XIII (FXIII) Val34Leu is the most important polymorphism of the A subunit in factor XIII gene. The aim of the present study was to develop an efficient method based on real time PCR with Fluorescence resonance energy transfer (FRET) detection and melting curve analysis for the detection of Val34Leu polymorphism.Specific primers were used to amplify the relevant fragment of the factor XIII-A gene and fluorescence resonance energy transfer hybridization probes were used for detection in a Rotor-Gene Q 5Plex HRM platform. Melting temperature (Tm) for the wild type was at 68.8, while Tm for homozygote mutant was at 63.8; heterozygote demonstrated both peaks.Our results showed that primers and probes propoesd in this study demonstrated a high specificity to identify wild type , heterozygous and homozygous mutantgenotypes. Due to the increasing molecular diagnosis in developing countries and the importance of identifying polymorphisms, this real time PCR assay is of great importance. An important advantage of this approach is the high sensitivity and specificity.http://dergipark.gov.tr/ijhsrp/issue/30684/331445factor XIIIval34leuFluorescence resonance energy transfer
collection DOAJ
language English
format Article
sources DOAJ
author Maryam NASER KAMJOO
Ali NAZEMI
spellingShingle Maryam NASER KAMJOO
Ali NAZEMI
VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000
International Journal of Health Services Research and Policy
factor XIII
val34leu
Fluorescence resonance energy transfer
author_facet Maryam NASER KAMJOO
Ali NAZEMI
author_sort Maryam NASER KAMJOO
title VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000
title_short VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000
title_full VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000
title_fullStr VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000
title_full_unstemmed VAL34LEU POLYMORPHISM DETECTION BY REAL TIME PCR ASSAY USING FLUORESCENCE RESONANCE ENERGY TRANSFER ON ROTOR-GENE 6000
title_sort val34leu polymorphism detection by real time pcr assay using fluorescence resonance energy transfer on rotor-gene 6000
publisher Rojan GÜMÜŞ
series International Journal of Health Services Research and Policy
issn 2602-3482
publishDate 2016-01-01
description Factor XIII (FXIII) Val34Leu is the most important polymorphism of the A subunit in factor XIII gene. The aim of the present study was to develop an efficient method based on real time PCR with Fluorescence resonance energy transfer (FRET) detection and melting curve analysis for the detection of Val34Leu polymorphism.Specific primers were used to amplify the relevant fragment of the factor XIII-A gene and fluorescence resonance energy transfer hybridization probes were used for detection in a Rotor-Gene Q 5Plex HRM platform. Melting temperature (Tm) for the wild type was at 68.8, while Tm for homozygote mutant was at 63.8; heterozygote demonstrated both peaks.Our results showed that primers and probes propoesd in this study demonstrated a high specificity to identify wild type , heterozygous and homozygous mutantgenotypes. Due to the increasing molecular diagnosis in developing countries and the importance of identifying polymorphisms, this real time PCR assay is of great importance. An important advantage of this approach is the high sensitivity and specificity.
topic factor XIII
val34leu
Fluorescence resonance energy transfer
url http://dergipark.gov.tr/ijhsrp/issue/30684/331445
work_keys_str_mv AT maryamnaserkamjoo val34leupolymorphismdetectionbyrealtimepcrassayusingfluorescenceresonanceenergytransferonrotorgene6000
AT alinazemi val34leupolymorphismdetectionbyrealtimepcrassayusingfluorescenceresonanceenergytransferonrotorgene6000
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