2012
DOI: 10.3923/ijps.2013.55.63
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Polymorphism of D-Loop Mitochondrial DNA Region and Phylogenetic in Five Indonesian Native Duck Population

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Cited by 14 publications
(16 citation statements)
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“…The genetic distance between Tegal and Magelang duck population closer than genetic distance between Gallang and Maggal duck (Table 4). The genetic distance between Tegal and Magelang duck in this study according to the previous study was reported by Purwantini et al (2013a) about 0.009-0, 691 based on D-loop mtDNA region. Gallang and Maggal ducks as the offspring of reciprocal crosses has a similarity and relationship tend to be closer to Tegal ducks compared with Magelang ducks.…”
Section: Polymorphisms Of Cytochrome B and Genetic Distancementioning
confidence: 96%
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“…The genetic distance between Tegal and Magelang duck population closer than genetic distance between Gallang and Maggal duck (Table 4). The genetic distance between Tegal and Magelang duck in this study according to the previous study was reported by Purwantini et al (2013a) about 0.009-0, 691 based on D-loop mtDNA region. Gallang and Maggal ducks as the offspring of reciprocal crosses has a similarity and relationship tend to be closer to Tegal ducks compared with Magelang ducks.…”
Section: Polymorphisms Of Cytochrome B and Genetic Distancementioning
confidence: 96%
“…South-East Asian duck population were closely related to the mallard duck (Anas platyrhynchos) that indicated by their mean overall genetic distance. Indonesian domestic ducks has a relatively closed genetic relationship with Anas Platyrhynchos and Anas zonorhyncha as shown by the variation of the genetic distance ranged from 0.000 to 0.786 (Purwantini et al, 2013a).…”
Section: Introductionmentioning
confidence: 99%
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“…PCR process was performed with condition predenaturation at 94°C for 5 minutes, denaturation at 94°C for 30 seconds, annealing at 51°C for 45 seconds, elongation (extension) at 72°C for 1 minute and post elongation at 72°C for 5 minutes. PCR was repeated for 35 cycles for optimum result (Purwantini et al, 2013). PCR product was separated by electrophoresis agarose gel 1% using buffer 1x TBE in Submarine Electrophoresis (Hoefer, USA).…”
Section: Laboratory Proceduresmentioning
confidence: 99%
“…Primers used were forward primer DL-AnasPF (L56) 5'-GTTGCGGGGTTATTTGGTTA-3 'and reverse primer DL-AnasPR (H773) 5'-CCA-TATACGCCAACCGTCTC-3' (Purwantini, Yuwanta, & Hartatik, 2013). The PCR program was pre-denaturation 94 °C for 5 minutes, denaturation 94 °C for 30 seconds, annealing 56.1 °C for 45 seconds, extension 72 °C for 1 min, and a final extension 72 °C for 5 minutes.…”
Section: Methodsmentioning
confidence: 99%