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Establishment of the optimal RAPD reaction system of Setosphaeria turcica

Gui Xiu-mei, Jinlin Zhang, Dong Jin-gao, AN Xin-long

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Abstract

The optimal RAPD reaction system of Setosphaeria turcica was established through experimentaion. In the total volume of 25 μL, there were 2 U Taq DNA polymerase, 2 mmol/L Mg~(2+), 200 μmol/L dNTP, 30 ng arbitrary primer, 1 μL 10×PCR buffer and 30 ng template DNA. Amplification was performed by the following program: 3 min at 94℃,40 cycles of 1min at 94℃, (1 min) at 37℃, 2 min at 72℃ and a final extention of 6 min at 72℃.

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What this paper is about

The optimal RAPD reaction system of Setosphaeria turcica was established through experimentaion. In the total volume of 25 μL, there were 2 U Taq DNA polymerase, 2 mmol/L Mg~(2+), 200 μmol/L dNTP, 30 ng arbitrary primer, 1 μL 10×PCR buffer and 30 ng template DNA. Amplification was performed by the following program: 3 min at 94℃,40 cycles of 1min at 94℃, (1 min) at 37℃, 2 min at 72℃ and a final extention of 6 min at 72℃.

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Available abstract

The optimal RAPD reaction system of Setosphaeria turcica was established through experimentaion. In the total volume of 25 μL, there were 2 U Taq DNA polymerase, 2 mmol/L Mg~(2+), 200 μmol/L dNTP, 30 ng arbitrary primer, 1 μL 10×PCR buffer and 30 ng template DNA. Amplification was performed by the following program: 3 min at 94℃,40 cycles of 1min at 94℃, (1 min) at 37℃, 2 min at 72℃ and a final extention of 6 min at 72℃.

Key concepts: RAPD, Primer (cosmetics), Biology, Polymerase chain reaction, Botany, Chemistry, Genetics, Gene

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