누에 RAPD - PCR 분석을 위한 기초연구

Reproducible the random amplified polymorphic DNAs(RAPDS) patterns were obtained in the two silkworm strains(J111, Galwon) by adjusting concentration optimized of Taq DNA polymerase(one unit), dNTP(200 μM), MgCl2,(1.5 mM) and template DNA(30 ng). In addition, anealing temperature ranging 35°C to 42°...

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Veröffentlicht in:한국잠사곤충학회지 1996-06, Vol.38 (1), p.7
Hauptverfasser: 황재삼, Jae Sam Hwang, 이진성, Jin Sung Lee, 이상몽, Sang Mong Lee, 강현아, Hyun Ah Kang, 황석조, Seok Jo Hwang, 서동상, Dong Sang Suh
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container_title 한국잠사곤충학회지
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creator 황재삼
Jae Sam Hwang
이진성
Jin Sung Lee
이상몽
Sang Mong Lee
강현아
Hyun Ah Kang
황석조
Seok Jo Hwang
서동상
Dong Sang Suh
description Reproducible the random amplified polymorphic DNAs(RAPDS) patterns were obtained in the two silkworm strains(J111, Galwon) by adjusting concentration optimized of Taq DNA polymerase(one unit), dNTP(200 μM), MgCl2,(1.5 mM) and template DNA(30 ng). In addition, anealing temperature ranging 35°C to 42°C by the adjusted condition was investigated and fixed at 35°C in this study. Variation among individuals and between male and female of Jam 113 strain was not authorized. DNA polymorphisms among silkworms were authorized by five RAPD markers using OPM04 random primer. Using the primer showing polymorphims between parents(J111, Galwon) in thirty three individuals, RAPD-PCR for F2 analysis was performed and segregated 3 : 1 in the F2 population. Consequently, RAPDS detected in the parents were obtained as genetic markers, which can be used for construction of genetic map for this industrially particular insect, silkworm Bombyx mori.
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In addition, anealing temperature ranging 35°C to 42°C by the adjusted condition was investigated and fixed at 35°C in this study. Variation among individuals and between male and female of Jam 113 strain was not authorized. DNA polymorphisms among silkworms were authorized by five RAPD markers using OPM04 random primer. Using the primer showing polymorphims between parents(J111, Galwon) in thirty three individuals, RAPD-PCR for F2 analysis was performed and segregated 3 : 1 in the F2 population. 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title 누에 RAPD - PCR 분석을 위한 기초연구
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