Establishment and Optimization of ISSR Reaction System for Pea
Farong Yang
Abstract
Farong Yang
Abstract
The optimum ISSR-PCR system for peas is established using ISSR-PCR amplification with five factors(DNA template,primer,dNTPs,Taq DNA polymerase and annealing temperature).The optimum reaction system(20 μL) contains 15 ng DNA template,0.15 mmol·L-1 dNTP,0.5 μmol·L-1 ISSR primer,1U Taq DNA polymerase.The suitable annealing temperature of primer 842 is 50℃.This reaction system will provide a technological base for genetic diversity analysis of pea germplasm,genetic map construction and gene location.
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The optimum ISSR-PCR system for peas is established using ISSR-PCR amplification with five factors(DNA template,primer,dNTPs,Taq DNA polymerase and annealing temperature).The optimum reaction system(20 μL) contains 15 ng DNA template,0.15 mmol·L-1 dNTP,0.5 μmol·L-1 ISSR primer,1U Taq DNA polymerase.The suitable annealing temperature of primer 842 is 50℃.This reaction system will provide a technological base for genetic diversity analysis of pea germplasm,genetic map construction and gene location.
Key concepts: Germplasm, Primer (cosmetics), Polymerase chain reaction, DNA, Genetic diversity, Taq polymerase, Biology, DNA profiling