2009Hubei nongye kexueRequires access

Optimization of RAPD-PCR Reaction Conditions for Sweet Potato

Xinsun Yang

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Abstract

In this paper,CTAB method was used to extract genomic DNA from sweet potato Xushu No.22.High purity DNA was selected as DNA template.Use random primers to run RAPD-PCR reaction.Through setting a gradient concentrations of the Taq DNA polymerase,MgCl2,dNTPs,DNA template and primers,the suitable conditions for RAPD-PCR reaction of sweet potato was obtained: 25.0 μL reaction system which contains 2.5 μL PCR 10×Buffer,0.15U Taq DNA polymerase;3.0 nmol·μL-1 MgCl2;0.6 nmol·μL-1 dNTPs;40 ng DNA template and 40 ng primer.

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What this paper is about

In this paper,CTAB method was used to extract genomic DNA from sweet potato Xushu No.22.High purity DNA was selected as DNA template.Use random primers to run RAPD-PCR reaction.Through setting a gradient concentrations of the Taq DNA polymerase,MgCl2,dNTPs,DNA template and primers,the suitable conditions for RAPD-PCR reaction of sweet potato was obtained: 25.0 μL reaction system which contains 2.5 μL PCR 10×Buffer,0.15U Taq DNA polymerase;3.0 nmol·μL-1 MgCl2;0.6 nmol·μL-1 dNTPs;40 ng DNA template and 40 ng primer.

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Available abstract

In this paper,CTAB method was used to extract genomic DNA from sweet potato Xushu No.22.High purity DNA was selected as DNA template.Use random primers to run RAPD-PCR reaction.Through setting a gradient concentrations of the Taq DNA polymerase,MgCl2,dNTPs,DNA template and primers,the suitable conditions for RAPD-PCR reaction of sweet potato was obtained: 25.0 μL reaction system which contains 2.5 μL PCR 10×Buffer,0.15U Taq DNA polymerase;3.0 nmol·μL-1 MgCl2;0.6 nmol·μL-1 dNTPs;40 ng DNA template and 40 ng primer.

Key concepts: RAPD, Primer (cosmetics), genomic DNA, DNA, Polymerase chain reaction, Taq polymerase, Biology, Molecular biology

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