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Multilevel D-loop PCR identification of hunting game

The control region of mtDNA (D-loop) was used for hair samples of the five hunting game species identification: red deer (Cervus elaphus), roe deer (Capreolus capreolus), fallow deer (Dama dama), mouflon (Ovis aries musimon), and wild boar (Sus scrofa). For D-loop multilevel PCR detection scheme was...

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Autores principales: Parkanyi, V., Ondruska, L., Vasicek, D., Slamecka, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881763/
https://www.ncbi.nlm.nih.gov/pubmed/27275406
http://dx.doi.org/10.1016/j.atg.2013.03.001
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author Parkanyi, V.
Ondruska, L.
Vasicek, D.
Slamecka, J.
author_facet Parkanyi, V.
Ondruska, L.
Vasicek, D.
Slamecka, J.
author_sort Parkanyi, V.
collection PubMed
description The control region of mtDNA (D-loop) was used for hair samples of the five hunting game species identification: red deer (Cervus elaphus), roe deer (Capreolus capreolus), fallow deer (Dama dama), mouflon (Ovis aries musimon), and wild boar (Sus scrofa). For D-loop multilevel PCR detection scheme was applied in six primers (CE CVZV 1 = 5′-GATCACGAGCTTGATCACCA-3′; CE CVZV 2 = 5′-AGGAGTGGGCGATTTTAGGT-3′; DD CVZV 3 = 5′-CGCGTGAAACCAACAACCCGC-3′; DD CVZV 4 = 5′-CCGGGTCGGGGCCTTAGACG-3′; SSW CVZV 5 = 5′-ACACGTGCGTACACGCGCATA-3′; SSW CVZV 6 = 5′-GGTGCCTGCT T TCGTAGCACG-3′) designed to identify unknown biological samples of the hunting game animals. The PCR reaction volume was 25 μl at conditions 95 °C for 2 min, 94 °C for 30 s, 60 °C for 30 s, 72 °C for 30 s, 35 cycles, with last extension at 72 °C for 10 min. D-loop mtDNA amplicons of the game animals are characterized with specific PCR product sizes depending on species: red deer = 163 bp and 140 bp, fallow deer = 280 bp and 138 bp, roe deer = 303 bp, 280 bp, 160 bp and 138 bp, mouflon = 299 bp and 178 bp, wild boar = 137 bp and 229 bp.
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spelling pubmed-48817632016-06-06 Multilevel D-loop PCR identification of hunting game Parkanyi, V. Ondruska, L. Vasicek, D. Slamecka, J. Appl Transl Genom Article The control region of mtDNA (D-loop) was used for hair samples of the five hunting game species identification: red deer (Cervus elaphus), roe deer (Capreolus capreolus), fallow deer (Dama dama), mouflon (Ovis aries musimon), and wild boar (Sus scrofa). For D-loop multilevel PCR detection scheme was applied in six primers (CE CVZV 1 = 5′-GATCACGAGCTTGATCACCA-3′; CE CVZV 2 = 5′-AGGAGTGGGCGATTTTAGGT-3′; DD CVZV 3 = 5′-CGCGTGAAACCAACAACCCGC-3′; DD CVZV 4 = 5′-CCGGGTCGGGGCCTTAGACG-3′; SSW CVZV 5 = 5′-ACACGTGCGTACACGCGCATA-3′; SSW CVZV 6 = 5′-GGTGCCTGCT T TCGTAGCACG-3′) designed to identify unknown biological samples of the hunting game animals. The PCR reaction volume was 25 μl at conditions 95 °C for 2 min, 94 °C for 30 s, 60 °C for 30 s, 72 °C for 30 s, 35 cycles, with last extension at 72 °C for 10 min. D-loop mtDNA amplicons of the game animals are characterized with specific PCR product sizes depending on species: red deer = 163 bp and 140 bp, fallow deer = 280 bp and 138 bp, roe deer = 303 bp, 280 bp, 160 bp and 138 bp, mouflon = 299 bp and 178 bp, wild boar = 137 bp and 229 bp. Elsevier 2013-03-14 /pmc/articles/PMC4881763/ /pubmed/27275406 http://dx.doi.org/10.1016/j.atg.2013.03.001 Text en © 2013 Elsevier B.V. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Parkanyi, V.
Ondruska, L.
Vasicek, D.
Slamecka, J.
Multilevel D-loop PCR identification of hunting game
title Multilevel D-loop PCR identification of hunting game
title_full Multilevel D-loop PCR identification of hunting game
title_fullStr Multilevel D-loop PCR identification of hunting game
title_full_unstemmed Multilevel D-loop PCR identification of hunting game
title_short Multilevel D-loop PCR identification of hunting game
title_sort multilevel d-loop pcr identification of hunting game
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881763/
https://www.ncbi.nlm.nih.gov/pubmed/27275406
http://dx.doi.org/10.1016/j.atg.2013.03.001
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