Gene expression for suboptimal mycorrhizal colonization in wild-type and jasmonic acid deficient spr2 tomato mutants

The data were obtained from wild-type tomato plants (roots or leaves) and spr2 mutants, with different degrees of mycorrhization.<br> Amplifications were performed using SYBR Green detection chemistry and run in triplicate in 96-well reaction plates with the CFX96 Touch Real-Time PCR Detection System (Bio-Rad, Hercules, CA, USA). The data was analyzed by the delta delta ct method.本数据集的样本取自野生型番茄植株（根或叶）及spr2突变体，所有样本均具有不同程度的菌根定植（mycorrhization）。<br>扩增反应采用SYBR Green检测化学法开展，在96孔反应板中设置三次重复，并通过CFX96 Touch实时荧光定量PCR检测系统（Real-Time PCR Detection System，Bio-Rad，美国加利福尼亚州赫拉克勒斯市）完成检测。数据采用ΔΔCt法（delta delta ct method）进行分析。