2016
DOI: 10.13057/biodiv/d170246
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Short Communication: Identification of Growth Hormone gene polymorphism for beef cattle in Pesisir Selatan District, West Sumatra, Indonesia

Abstract: . Blood samples were collected from 66 individuals consist of 15 Pesisir cattle, 15 SimPes cattle, 15 SimPO cattle, 15 Bali cattle and 6 PO cattle. DNA was extracted from each blood samples after SDS-proteinase K digestion, and used for PCR-amplification for a region of growth hormone gene (211 bp), and then the PCR products were analyzed for restriction fragment length polymorphism (RFLP) using AluI restriction enzyme. The results showed that GH gene of Pesisir, PO and Bali cattle are monomorphic, which frequ… Show more

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Cited by 5 publications
(10 citation statements)
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“…DNA was isolated according to the procedure conducted by Putra et al (2016). Two hundreds microliters of blood sample in 1.5 mL microtubes were added with 800 µL of buffer A ((0.32 M Sucrose (Himedia, India); 10 mM TrisHCL pH 7.5; 5 mM MgCl 2 (Merck, Germany), 1% Triton X-100 (applichem); DDW)), and it was mixed carefully.…”
Section: Dna Isolationmentioning
confidence: 99%
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“…DNA was isolated according to the procedure conducted by Putra et al (2016). Two hundreds microliters of blood sample in 1.5 mL microtubes were added with 800 µL of buffer A ((0.32 M Sucrose (Himedia, India); 10 mM TrisHCL pH 7.5; 5 mM MgCl 2 (Merck, Germany), 1% Triton X-100 (applichem); DDW)), and it was mixed carefully.…”
Section: Dna Isolationmentioning
confidence: 99%
“…Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RLFP) method was employed for genotype analysis of GH891 using MspI restriction enzyme, according to the procedure of Putra et al (2013) and Putra et al (2016). Briefly, 10 µL of PCR products were digested using 3U of MspI enzyme (Fermentas, Life Science) and incubated for 5 hours at 37 o C. PCR-RFLP products were run on 2% agarose gel…”
Section: Polymerase Chain Reaction-restriction Fragment Length Polymomentioning
confidence: 99%
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“…Polimorfisme di daerah exon dan intron memiliki potensi digunakan sebagai penanda genetik untuk perbaikan genetik populasi (Falaki et al, 1996). Telah banyak penelitian mencari hubungan antara varian gen ini dan sifat-sifat produksi (Tatsuda et al, 2008;Yardibi et al, 2009;Matsuhashi et al, 2010;Mohammadabadi et al, 2010;Maylinda, 2011;Sami, 2010;Sami et al, 2011;Moravčíková et al, 2012;Putra et al, 2015). Yurnalis et al (2013) telah meneliti keragam gen GH sapi Pesisir pada exon 4 dan sebagian intron 4 sedangkan penelitian tentang keragaman gen GH pada daerah ujung belum pernah dilakukan.…”
Section: Pendahuluanunclassified
“…The GH gene polymorphism was intensively studied in many cattle breeds including local Indonesian cattle breeds (Paputungan et al 2012;Hartatik et al 2013;Putra et al 2014;Putra et al 2016) but limited reports for the Indonesian SO cattle GH gene. Up to present, information about the SO cattle GH gene polymorphism is limited only in the intron region (Agung et al 2017).…”
Section: Introductionmentioning
confidence: 99%