The suitable PCR system for loquat were found: μl reaction volume with .μl 0×PCR buffer, .pμlMg~(+), 0.μl Taq polymerase, 0.μl dNTP, .μl primer, .7μl ddH_0, ul template DNA.
The suitable PCR system for loquat were found: μl reaction volume with .μl 0×PCR buffer, .pμlMg~(+), 0.μl Taq polymerase, 0.μl dNTP, .μl primer, .7μl ddH_0, ul template DNA.
通过筛选优化了更加适宜枇杷的RAPD扩增体系：.μl 0×PCR buffer，.μlMg~(+)，0.μl Taq酶，0.μl dNTP，.μl随机引物，.7μl ddH_O，μl模板DNA。