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                <text>H, Herrialfian</text>
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                <text>Widayanti, Rini</text>
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                <text>Wijayanto, Hery</text>
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                <text>J, Jalaluddin</text>
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                <text>Penelitian ini bertujuan mengkaji keragaman genetik gen penyandi ND4 pada Tarsius bancanus, T. b. borneanus, T. dianae dan T. spectrum dan untuk penegakan taksonominya. Deoxyribonucleic acid (DNA) diisolasi dari biopsi jaringan masing-masing spesies Tarsius dengan cara diekstraksi untuk digunakan sebagai DNA cetakan dalam proses amplifikasi dengan metode polymerase chain reaction (PCR). Primer yang digunakan dalam penelitian ini didesain untuk mengamplifikasi gen ND4 dan dilanjutkan dengan elektroforesis. Produk PCR hasil amplifikasi yang telah dimurnikan, selanjutnya dipergunakan sebagai DNA cetakan untuk reaksi penentuan runutan nukleotida. Runutan nukleotida gen ND4 hasil pengurutan dilakukan penjajaran berganda dengan primata lain yang diambil dari Genbank menggunakan Clustal W. Selain berdasarkan runutan nukleotida, gen ND4 dianalisis berdasarkan runutan asam amino dari basa-basa yang diterjemahkan mengikuti vertebrate mitochondrial translation code yang ada pada program MEGA versi 4.1. Konstruksi pohon filogenetika menggunakan metode neighbor joining. Hasil penelitian menunjukkan dari 1378 nukleotida ditemukan 119 situs yang bersifat beragam. Jarak genetika berdasarkan nukleotida gen ND4 yang dihitung menggunakan model dua parameter Kimura, terdapat nilai paling kecil 0,6%, nilai terbesar 13%, dan nilai rata-rata sebesar 6,1%. Filogram berdasarkan hasil runutan nukleotida gen ND4 yang menggunakan metode neighbor joining, dapat mengidentifikasi dan membedakan percabangan antar spesies Tarsius.</text>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/1247</text>
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                <text>10.21157/j.ked.hewan.v8i1.1247</text>
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                <text>en</text>
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            <name>Publisher</name>
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                <text>Syiah Kuala University</text>
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                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 8, No 1 (2014): J. Ked. Hewan</text>
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                <text>Jurnal Kedokteran Hewan; Vol 8, No 1 (2014): J. Ked. Hewan</text>
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                <text>2502-5600</text>
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                <text>1978-225X</text>
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                <text>KAJIAN DIVERSITI GENETIKA Tarsius sp. ASAL INDONESIA MENURUT URUTAN GEN NADH DEHIDROGENASE SUBUNIT 4 (ND4)</text>
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                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
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            <name>Creator</name>
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                <text>Saptiani, Gina</text>
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                <text>Prayitno, Slamet Budi</text>
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                <text>Anggoro, Sutrisno</text>
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                <text>Untuk mengetahui potensi antibakteri dan konsentrasi optimal jeruju (Acanthus ilicifolius), dilakukan uji daya hambat ekstrak dan fraksi daun terhadap pertumbuhan Vibrio harveyi, bakteri penyebab penyakit pada udang. Daun yang sudah dikeringanginkan diekstraksi dengan metanol, sehingga didapatkan ekstrak kasar (crude). Sebagian dari ekstrak kasar dilakukan fraksinasi dengan metode kolom silika gel dengan pelarut n-heksan, etil asetat, n-butanol, etanol, dan metanol. Uji daya hambat dilakukan dengan agar disc diffusion method. Perlakuan yang diberikan adalah ekstrak kasar, fraksi n-heksan, etil asetat, n-butanol, etanol, dan metanol yang masing-masing konsentrasinya 50-1000 ppm, yang diberikan pada kultur V. harveyi pada media Triptic Soy Agar (TSA). Fraksi etil asetat menunjukkan daya hambat terbaik (12 mm), diikuti ekstrak (11,33 mm), dan fraksi n-butanol (11 mm).</text>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/558</text>
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                <text>10.21157/j.ked.hewan.v7i1.558</text>
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            <description>A language of the resource</description>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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                <text>Syiah Kuala University</text>
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            <description>A related resource</description>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/558/467</text>
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            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="49318">
                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 7, No 1 (2013): J. Ked. Hewan</text>
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                <text>Jurnal Kedokteran Hewan; Vol 7, No 1 (2013): J. Ked. Hewan</text>
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                <text>2502-5600</text>
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                <text>1978-225X</text>
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                <text>POTENSI ANTIBAKTERI EKSTRAK DAUN JERUJU (Acanthus ilicifolius) TERHADAP Vibrio harveyi SECARA IN VITRO</text>
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                <text/>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="136908">
                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
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              <elementText elementTextId="136909">
                <text>http://creativecommons.org/licenses/by-sa/4.0</text>
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              <name>Title</name>
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                  <text>e-Journal USK</text>
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            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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              <elementText elementTextId="49268">
                <text>Wahyuni, Sri</text>
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                <text>Agungpriyono, Srihadi</text>
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                <text>Agil, Muhammad</text>
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                <text>Yusuf, Tuty Laswardi</text>
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            <name>Date</name>
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                <text>2011-03-01</text>
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                <text>Penelitian ini bertujuan menggambarkan morfologi pertumbuhan ranggah velvet (RV) dua ekor muncak jantan (M1 dan M2) yang dipelihara di kandang penelitian secara terpisah. Tanggal lepas ranggah dan hari pertama percabangan RV serta awal pengelupasan kulit velvet diamati dan dicatat. Pengukuran meliputi panjang dan diameter ranggah velvet utama (RVU) dan ranggah velvet cabang (RVC) dexter et sinister, serta durasi pertumbuhan RV. Rataan ± SD panjang dan diameter maksimum RVU dan RVC muncak M1 adalah 148,25±1,12 mm; 46,26±0,68 mm (panjang), 19,21±2,35 mm; 9,12±0,21 mm (diameter) dengan durasi pertumbuhan 104 hari; sedangkan muncak M2 berturut-turut adalah: 146,44±1,58 mm; 46,94±1,97 mm (panjang); 13,65±1,27 mm; 8,49±0,29 mm (diameter) dengan durasi pertumbuhan 98 hari. Tidak terdapat perbedaan tahapan pertumbuhan RVU dan RVC antara muncak M2 dan M1, namun berbeda pada ukuran RV dan durasi pertumbuhannya. Muncak M2 memasuki ranggah keras setelah pengelupasan kulit velvet lebih cepat dibandingkan M1. Dapat disimpulkan bahwa ukuran pertumbuhan RV berkorelasi erat dengan faktor umur, berat badan, dan postur tubuh muncak jantan.</text>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/419</text>
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                <text>10.21157/j.ked.hewan.v5i1.419</text>
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                <text>eng</text>
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                <text>Syiah Kuala University</text>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/419/388</text>
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                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 5, No 1 (2011): J. Ked. Hewan</text>
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                <text>Jurnal Kedokteran Hewan; Vol 5, No 1 (2011): J. Ked. Hewan</text>
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                <text>2502-5600</text>
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                <text>MORFOLOGI DAN MORFOMETRI PERTUMBUHAN RANGGAH VELVET MUNCAK JANTAN (Muntiacus muntjak muntjak)</text>
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            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="136868">
                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
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                <text>http://creativecommons.org/licenses/by-sa/4.0</text>
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                <text>Muchtaromah, Bayyinatul</text>
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                <text>Sumitro, Sutiman B.</text>
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                <text>Penelitian ini bertujuan mengetahui pengaruh dosis dan lama inkubasi anti MPS ecto-CIK dalam menghambat viabilitas spermatozoa kambing dan sapi. Rancangan penelitian yang digunakan adalah rancangan acak lengkap (RAL) dengan pola faktorial yang terdiri atas 2 faktor yakni dosis pengenceran (0, 5, 10, dan 15 µl) dan lama inkubasi (5, 30, 60, dan 120 menit) masing-masing 6 kali ulangan. Data yang diperoleh dianalisis dengan analisis varian dua arah, yang dilanjutkan dengan uji jarak Duncan dengan taraf signifikansi 5%. Pemberian anti MPS ecto-CIK membran spermatozoa kambing dengan konsentrasi 0, 5, 10, dan 15 µl dan lama inkubasi 5, 30, 60, dan 120 menit berpengaruh signifikan terhadap viabilitas spermatozoa kambing dan sapi (P&lt;0,05). Perlakuan anti MPS ecto-CIK pada dosis 15 µl dan lama inkubasi 120 menit terhadap spermatozoa kambing dan sapi merupakan perlakuan yang paling optimal dalam menghambat viabilitas spermatozoa kambing (45,50±11,16 dan 44,87±9,40%) dan sapi (39,08±14,40 dan 36,67±11,93%).</text>
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                <text>KEMAMPUAN ANTI MAYOR PHYSIOLOGICAL PROTEIN SUBSTRAT ECTO CYCLIC AMP INDEPENDENT SERIN/THEONIN PROTEIN KINASE (MPS ecto-CIK) DALAM MENGHAMBAT VIABILITAS SPERMATOZOA KAMBING DAN SAPI</text>
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                <text>Penelitian ini menggunakan klorin dalam bentuk natrium hipoklorit yang dipaparkan secara in vitro untuk menguji kemampuan oosit ikan lele dalam menoleransi kehadiran klorin sebagai bahan oksidatif stres dalam medium kultur. Konsentrasi klorin yang digunakan adalah 0, 10, 20, 40, 80, 160, dan 320 μM. Hasil penelitian menunjukkan bahwa semakin tinggi konsentrasi paparan semakin rendah jumlah oosit yang mampu bertahan hidup hingga 4 jam pengamatan. Konsentrasi klorin 320 μM menghasilkan jumlah oosit yang mampu bertahan hidup paling optimum. Disimpulkan bahwa oosit ikan lele mampu menoleransi kehadiran bahan oksidatif stres dalam medium kultur dengan konsentrasi paparan klorin sebanyak 320 μM.</text>
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                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 8, No 1 (2014): J. Ked. Hewan</text>
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                <text>KEMAMPUAN OOSIT IKAN LELE (Clarias grapienus) DALAM MENOLERANSI KLORIN SEBAGAI BAHAN OKSIDATIF STRES</text>
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            <description>Information about rights held in and over the resource</description>
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                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
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                <text>Tujuan dari penelitian ini adalah melakukan analisis kuantitatif risiko mengonsumsi ayam panggang apabila terjadi salah penanganan. Proses pemanggangan yang digunakan pada penelitian ini menggunakan suhu dan waktu komersial yaitu 150 C selama 30 menit. Simulasi penambahan kultur Campylobacter sp. 106 cfu/ml sebelum dilakukan pemanggangan dilakukan untuk mengetahui angka reduksi Campylobacter sp. Model probabilitas digunakan untuk memperkirakan variabilitas data yang digunakan pada penelitian ini adalah model beta poisson. Hasil yang diperoleh adalah terjadi penurunan jumlah mikroorganisme sebanyak 2 log cfu/gram dan peluang sakit bagi manusia yang mengonsumsi daging ayam yang dipanggang berkisar antara 9 dari 1.000 manusia.</text>
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                <text>KAJIAN RISIKO Campylobacter sp. PADA AYAM PANGGANG</text>
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                <text>Virus avian influenza (AI) merupakan virus dengan materi genetik RNA single-stranded sense negatif, beramplop yang termasuk dalam famili Orthomyxoviridae. Onestep simplex reverse transcriptase-polymerase chain reaction (RT-PCR) merupakan salah satu metode diagnosis yang dapat diandalkan untuk mendeteksi virus AI. Tujuan dari penelitian ini adalah untuk menerapkan metode diagnosis cepat virus AI pada spesimen lapangan secara langsung dari pasar unggas berdasarkan amplifikasi RT-PCR gen M dan H5 dengan metode yang berbasis onestep simplex RT-PCR tanpa melalui proses inokulasi dan propagasi virus AI dalam telur ayam berembrio (TAB). Sebanyak 35 sampel spesimen lapangan dari swab trakea unggas yang berasal dari pasar unggas di Terban, Kotamadya Yogyakarta digunakan dalam penelitian ini. Amplifikasi DNA secara onestep simplex RT-PCR pada gen matriks (M) dilakukan terhadap seluruh sampel. Pada sampel-sampel yang menunjukkan hasil positif pada amplifikasi gen M kemudian dilakukan amplifikasi RT-PCR secara lebih lanjut untuk gen H5 virus AI. Produk hasil amplifikasi RT-PCR gen M dan H5 divisualisasikan menggunakan elektroforesis gel agarose konsentrasi 1% dengan pewarnaan SYBR® Safe DNA Gel Staining. Hasil amplifikasi RT-PCR gen M menunjukkan bahwa dari 35 sampel diperoleh 8 sampel positif terinfeksi virus AI tipe A yang ditunjukkan dengan adanya fragmen DNA sebesar 200 bp, sedangkan hasil amplifikasi gen H5 sebanyak 5 dari 8 sampel-sampel tersebut merupakan virus AI tipe A subtipe H5 yang ditunjukkan dengan adanya fragmen DNA sebesar 545 bp. Diagnosis cepat virus AI tipe A subtipe H5 secara langsung dari spesimen lapangan di pasar unggas dapat dilakukan dengan metode onestep simplex RT-PCR, namun metode diagnosis tersebut tidak dapat mendeteksi keberadaan virus AI dalam sampel yang virusnya terlalu sedikit.</text>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/346/331</text>
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                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 6, No 1 (2012): J. Ked. Hewan</text>
              </elementText>
              <elementText elementTextId="49164">
                <text>Jurnal Kedokteran Hewan; Vol 6, No 1 (2012): J. Ked. Hewan</text>
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              <elementText elementTextId="49165">
                <text>2502-5600</text>
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                <text>1978-225X</text>
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                <text>DIAGNOSIS CEPAT VIRUS AVIAN INFLUENZA TIPE A SUBTIPE H5 DARI SPESIMEN LAPANGAN DENGAN METODE ONESTEP SIMPLEX RT-PCR</text>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="137669">
                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
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              <elementText elementTextId="137670">
                <text>http://creativecommons.org/licenses/by-sa/4.0</text>
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          <element elementId="39">
            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
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              <elementText elementTextId="49107">
                <text>S, Sugito</text>
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                <text>N, Nurliana</text>
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              <elementText elementTextId="49110">
                <text>Aliza, Dwinna</text>
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                <text>S, Samadi</text>
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                <text>Penelitian  ini dilakukan untuk mengetahui  efek  suplementasi tepung daun jaloh  (Salix tetrasperma Roxb) (TDJ) dalam pakan  terhadap  nilai
diferensial leukosit dan ketahanan hidup setelah uji tantang dengan Aeromonas hydrophila pada ikan nila (Oreochromis niloticus) yang dipelihara 
pada akuarium diberi peningkatan suhu lingkungan.  Penelitian ini menggunakan rancangan acak lengkap faktorial 2x4. Faktor pertama adalah 
penambahan jumlah tepung daun jaloh dalam pakan   yaitu: 0% (P1), 5% (P2), 10% (P3), dan 15% (P4) dari berat pakan  dan faktor kedua adalah
suhu air dalam akuarium  yaitu 29±1  C (S1) dan 35±1 C (S2), sehingga didapat 8 kombinasi perlakuan  yaitu: P1S1, P2S1, P3S1, P4S1, P1S2, 
P2S2, P3S2, dan P4S2 dengan ulangan 10 ekor ikan per perlakuan. Sebanyak 80 ekor ikan nila dengan bobot badan 40-50 g secara acak dibagi ke 
dalam 8 perlakuan. Perlakuan dilakukan selama 30 hari. Pada hari ke 31 dilakukan pengambilan sampel darah dan uji tantang. Hasil penelitian ini 
menunjukkan bahwa suplementasi pakan dengan TDJ pada konsentrasi 5-15% tidak berpengaruh terhadap nilai diferensial leukosit ikan nila yang 
dipelihara pada suhu lingkungan yang berbeda.  Suplementasi TDJ dalam pakan sebanyak 5-10% dapat mengurangi kematian ikan akibat infeksi 
Aeromonas hydrophila  terutama  pada suhu 35±1 C.  Dari hasil penelitian ini dapat disimpulkan bahwa ikan nila yang dipelihara pada akuarium
dengan suhu air 35±1 C dan diberi pakan yang disuplementasi TDJ 5-10% dapat meningkatkan daya tahan tubuh ikan nila.</text>
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              <elementText elementTextId="49118">
                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/2652</text>
              </elementText>
              <elementText elementTextId="137965">
                <text>10.21157/j.ked.hewan.v8i2.2652</text>
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            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49120">
                <text>eng</text>
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            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
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              <elementText elementTextId="49122">
                <text>Syiah Kuala University</text>
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            <description>A related resource</description>
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                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/2652/2504</text>
              </elementText>
            </elementTextContainer>
          </element>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49126">
                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
              </elementText>
              <elementText elementTextId="137966">
                <text>http://creativecommons.org/licenses/by-sa/4.0</text>
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            <description>A related resource from which the described resource is derived</description>
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              <elementText elementTextId="49128">
                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 8, No 2 (2014): J. Ked. Hewan</text>
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              <elementText elementTextId="49130">
                <text>Jurnal Kedokteran Hewan; Vol 8, No 2 (2014): J. Ked. Hewan</text>
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                <text>2502-5600</text>
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            <name>Title</name>
            <description>A name given to the resource</description>
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              <elementText elementTextId="49134">
                <text>DIFERENSIAL LEUKOSIT DAN KETAHANAN HIDUP PADA UJI  TANTANG Aeromonas hydrophila IKAN NILA YANG DIBERI STRES PANAS DAN SUPLEMENTASI TEPUNG DAUN JALOH DALAM PAKAN</text>
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              <name>Title</name>
              <description>A name given to the resource</description>
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                  <text>e-Journal USK</text>
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        <name>Dublin Core</name>
        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <element elementId="39">
            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49077">
                <text>Helmi, Teuku Zahrial</text>
              </elementText>
              <elementText elementTextId="49079">
                <text>Widayanti, Rini</text>
              </elementText>
              <elementText elementTextId="49081">
                <text>Haryanto, Aris</text>
              </elementText>
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          <element elementId="40">
            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="49082">
                <text>2014-03-01</text>
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            </elementTextContainer>
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          <element elementId="41">
            <name>Description</name>
            <description>An account of the resource</description>
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              <elementText elementTextId="49083">
                <text>Tujuan dari penelitian ini adalah mengidentifikasi keberadaan gen M, H5, dan N1 virus avian influenza (AI) melalui metode single step multiplex reverse transcriptase-polymerase chain reaction (RT-PCR), sebagai acuan untuk peneguhan diagnosis secara molekuler virus AI di Provinsi Aceh. Penelitian ini menggunakan 11 isolat virus AI asal Provinsi Aceh yang diperoleh dari Laboratorium Balai Penyidikan dan Pengujian Veteriner (BPPV) Regional I Medan di Sumatera Utara dari tahun 2006-2008. Penelitian dilakukan di Laboratorium Virologi BPPV Regional I di Medan, Sumatera Utara. Amplifikasi terhadap gen matriks (M) virus AI menggunakan metode simplex RT-PCR. Hasil simplex RT-PCR terhadap gen M diperoleh 10 isolat yang menunjukkan pita deoxyribonucleic acid (DNA) pada 276 bp dan satu isolat yang tidak muncul, kemudian dilanjutkan dengan metode single step multiplex RT-PCR menggunakan pasangan primer gen penyandi protein N1, H5, dan M. Produk PCR 131 bp (N1), 189 bp (H5), dan 276 bp (M) muncul sebagai hasil elektroforesis dari semua isolat virus AI. Semua virus AI yang mewabah dari tahun 2006-2008 di Provinsi Aceh termasuk ke dalam virus influenza A subtipe H5N1.</text>
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            <name>Format</name>
            <description>The file format, physical medium, or dimensions of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49085">
                <text>application/pdf</text>
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          <element elementId="43">
            <name>Identifier</name>
            <description>An unambiguous reference to the resource within a given context</description>
            <elementTextContainer>
              <elementText elementTextId="49087">
                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/1265</text>
              </elementText>
              <elementText elementTextId="136701">
                <text>10.21157/j.ked.hewan.v8i1.1265</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="44">
            <name>Language</name>
            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49089">
                <text>eng</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="49091">
                <text>Syiah Kuala University</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="46">
            <name>Relation</name>
            <description>A related resource</description>
            <elementTextContainer>
              <elementText elementTextId="49092">
                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/1265/1152</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="48">
            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="49093">
                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 8, No 1 (2014): J. Ked. Hewan</text>
              </elementText>
              <elementText elementTextId="49095">
                <text>Jurnal Kedokteran Hewan; Vol 8, No 1 (2014): J. Ked. Hewan</text>
              </elementText>
              <elementText elementTextId="49097">
                <text>2502-5600</text>
              </elementText>
              <elementText elementTextId="136704">
                <text>1978-225X</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="50">
            <name>Title</name>
            <description>A name given to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49099">
                <text>PENENTUAN SUBTIPE VIRUS AVIAN INFLUENZA DENGAN METODE SINGLE STEP MULTIPLEX REVERSE TRANSCRIPTASE- POLYMERASE CHAIN REACTION (RT-PCR) ISOLAT ASAL PROVINSI ACEH</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="51">
            <name>Type</name>
            <description>The nature or genre of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49101">
                <text>info:eu-repo/semantics/article</text>
              </elementText>
              <elementText elementTextId="49102">
                <text>info:eu-repo/semantics/publishedVersion</text>
              </elementText>
              <elementText elementTextId="49103">
                <text>Peer-reviewed Article</text>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="37">
            <name>Contributor</name>
            <description>An entity responsible for making contributions to the resource</description>
            <elementTextContainer>
              <elementText elementTextId="136700">
                <text/>
              </elementText>
            </elementTextContainer>
          </element>
          <element elementId="47">
            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="136702">
                <text>Copyright (c) 2016 by author and J. Ked. Hewan</text>
              </elementText>
              <elementText elementTextId="136703">
                <text>http://creativecommons.org/licenses/by-sa/4.0</text>
              </elementText>
            </elementTextContainer>
          </element>
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    <collection collectionId="26">
      <elementSetContainer>
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          <name>Dublin Core</name>
          <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
          <elementContainer>
            <element elementId="50">
              <name>Title</name>
              <description>A name given to the resource</description>
              <elementTextContainer>
                <elementText elementTextId="31035">
                  <text>e-Journal USK</text>
                </elementText>
              </elementTextContainer>
            </element>
          </elementContainer>
        </elementSet>
      </elementSetContainer>
    </collection>
    <elementSetContainer>
      <elementSet elementSetId="1">
        <name>Dublin Core</name>
        <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <element elementId="39">
            <name>Creator</name>
            <description>An entity primarily responsible for making the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49047">
                <text>M. Kaiin, Ekayanti</text>
              </elementText>
              <elementText elementTextId="49049">
                <text>Djuwita, Ita</text>
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              <elementText elementTextId="49050">
                <text>Yusuf, Tuty L.</text>
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              <elementText elementTextId="49051">
                <text>Setiadi, M. Agus</text>
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            </elementTextContainer>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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              <elementText elementTextId="49053">
                <text>2013-03-01</text>
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            <description>An account of the resource</description>
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                <text>Penelitian ini bertujuan isolasi dan purifikasi sel Leydig dengan menggunakan gradien Nycodenz untuk meningkatkan jumlah perolehan sel Leydig yang hidup setelah purifikasi dan kultur. Isolasi dan purifikasi sel Leydig dilakukan dengan perlakuan gradien Nycodenz 3 kolom (5, 10, dan 15% sebagai Nycodenz I) dan 5 kolom (4, 8, 10, 12, dan 15% sebagai Nycodenz II) serta gradien Percoll 5 kolom (21, 26, 34, 40 dan 60%) sebagai kontrol. Parameter yang diamati adalah konsentrasi, kemurnian, dan viabilitas sel Leydig setelah isolasi dan purifikasi serta kultur in vitro. Hasil yang diperoleh menunjukkan bahwa isolasi dan purifikasi sel Leydig dengan gradien Nycodenz (I dan II) secara nyata (P&lt;0,01) menghasilkan konsentrasi sel yang lebih rendah dibandingkan dengan gradien Percoll. Namun penggunaan gradien Nycodenz II c enderung menghasilkan kemurnian sel yang lebih tinggi (91,40%) dibandingkan dengan Nycodenz I (85,53%). Hasil tersebut tidak berbeda nyata dibandingkan dengan gradien Percoll (92,20%). Viabilitas sel Leydig pada semua perlakuan hampir sama yaitu 98%. Namun demikia n, setelah dikultur selama 3 hari, konsentrasi sel Leydig pada perlakuan Percoll (2,44x106 sel/ml) dan Nycodenz I (3,21x106 sel/ml) secara statistik (P&lt;0,05) lebih rendah dan dibandingkan dengan Nycodenz II (3,88x10 6 sel/ml), sedangkan viabilitas sel Leydig setelah dikultur pada gradien Nycodenz I (90,00%) dan Nycodenz II (91,17%) secara sangat nyata (P&lt;0,01) menghasilkan viabilitas yang lebih tinggi dibandingkan dengan gradien Percoll (82,30%). Berdasarkan hasil tersebut dapat disimpulkan bahwa penggunaan gradien Nycodenz II efektif untuk mempurifikasi sel Leydig dan setelah dikultur menghasilkan konsentrasi dan viabilitas sel yang lebih tinggi dibandingkan dengan gradien Percoll.</text>
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            <description>The file format, physical medium, or dimensions of the resource</description>
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                <text>application/pdf</text>
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            <description>An unambiguous reference to the resource within a given context</description>
            <elementTextContainer>
              <elementText elementTextId="49058">
                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/580</text>
              </elementText>
              <elementText elementTextId="137099">
                <text>10.21157/j.ked.hewan.v7i1.580</text>
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            <name>Language</name>
            <description>A language of the resource</description>
            <elementTextContainer>
              <elementText elementTextId="49059">
                <text>eng</text>
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          <element elementId="45">
            <name>Publisher</name>
            <description>An entity responsible for making the resource available</description>
            <elementTextContainer>
              <elementText elementTextId="49061">
                <text>Syiah Kuala University</text>
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            </elementTextContainer>
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            <name>Relation</name>
            <description>A related resource</description>
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              <elementText elementTextId="49063">
                <text>http://jurnal.unsyiah.ac.id/JKH/article/view/580/490</text>
              </elementText>
            </elementTextContainer>
          </element>
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            <name>Source</name>
            <description>A related resource from which the described resource is derived</description>
            <elementTextContainer>
              <elementText elementTextId="49065">
                <text>Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences; Vol 7, No 1 (2013): J. Ked. Hewan</text>
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              <elementText elementTextId="49066">
                <text>Jurnal Kedokteran Hewan; Vol 7, No 1 (2013): J. Ked. Hewan</text>
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