| 摘要 |
PROBLEM TO BE SOLVED: To shorten a creation time of a PCR product.SOLUTION: In a nucleic acid amplification device 50 of the present invention, a control part 80, after giving heat to a nucleic acid covering body covering template nucleic acid for a predetermined period at temperature which is set in order to break the body, controls a moving mechanism 60 so as to repeat a cycle having a denaturation step of allowing a droplet 20 to stay in a first region 36A which is set to denaturation temperature of target nucleic acid and a synthesis step of allowing the droplet 20 to stay in a second region 36B which is set to synthesis temperature of the target nucleic acid for a plurality of times.SELECTED DRAWING: Figure 7 |
