Development of mitochondrial 12S rRNA gene for identification of dog and rat in beef using multiplex PCR

The 12S rRNA gene is one of unique regions in mitochondrial genome usually used for phylogenetic studies and species identification. The objective of present study was to develop species specific primers from mitochondrial 12S rRNA gene for identification of dog and rat in beef by using multiplex PC...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Cahyadi, M. (Yazar), Taufik, I. M. (Yazar), Pramono, A. (Yazar), Abdurrahman, Z. H. (Yazar)
Materyal Türü: EJournal Article
Baskı/Yayın Bilgisi: Diponegoro University, 2019-03-21.
Konular:
Online Erişim:Get Fulltext
Get Fulltext
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
LEADER 02905 am a22003133u 4500
001 JITAA_UNDIP_19471_pdf
042 |a dc 
100 1 0 |a Cahyadi, M.  |e author 
100 1 0 |e contributor 
700 1 0 |a Taufik, I. M.  |e author 
700 1 0 |a Pramono, A.  |e author 
700 1 0 |a Abdurrahman, Z. H.  |e author 
245 0 0 |a Development of mitochondrial 12S rRNA gene for identification of dog and rat in beef using multiplex PCR 
260 |b Diponegoro University,   |c 2019-03-21. 
500 |a https://ejournal.undip.ac.id/index.php/jitaa/article/view/19471 
520 |a The 12S rRNA gene is one of unique regions in mitochondrial genome usually used for phylogenetic studies and species identification. The objective of present study was to develop species specific primers from mitochondrial 12S rRNA gene for identification of dog and rat in beef by using multiplex PCR assay. Three primer pairs of mitochondrial 12S rRNA gene specific for bovine, dog and rat were designed and selected to evaluate their specificity and fidelity. Moreover, a total of twelve DNA samples extracted from meat tissue were also prepared to test those primers using simplex and multiplex PCR. The PCR products were then visualized using 2% of agarose gel under the UV light and three of them were sequenced. In addition, sequence data were analyzed using Clustal Omega software and BLAST. The result showed that simplex PCR assay successfully amplified DNA targets which are respectively indicated by 155 bp (bovine), 244 bp (dog), and 491 bp (rat) of DNA bands. Furthermore, DNA sample sequences were identically similar to reference sequence used in this study. Multiplex and simplex PCR analyses also indicated that these primer pairs specifically amplified DNA target for each species in the samples containing various species. The results suggested that designed primers in this study could be used to identify dog and rat in raw beef containing these species meat. Further experiment should be conducted using meat-processed products and commercial meat products as samples. 
540 |a Copyright (c) 2019 Journal of the Indonesian Tropical Animal Agriculture 
546 |a eng 
690 |a beef; dog; rat; species identification; 12S rRNA 
655 7 |a info:eu-repo/semantics/article  |2 local 
655 7 |a info:eu-repo/semantics/publishedVersion  |2 local 
655 7 |a Peer-reviewed Article  |2 local 
786 0 |n Journal of the Indonesian Tropical Animal Agriculture; Vol 44, No 1 (2019): March; 10-18 
786 0 |n 2460-6278 
786 0 |n 2087-8273 
787 0 |n https://ejournal.undip.ac.id/index.php/jitaa/article/view/19471/pdf 
787 0 |n https://ejournal.undip.ac.id/index.php/jitaa/article/downloadSuppFile/19471/2650 
856 4 1 |u https://ejournal.undip.ac.id/index.php/jitaa/article/view/19471/pdf  |z Get Fulltext 
856 4 1 |u https://ejournal.undip.ac.id/index.php/jitaa/article/downloadSuppFile/19471/2650  |z Get Fulltext