大豆腺苷酸激酶基因GmADK 的克隆与表达分析
盖江涛, 赵团结, 李艳* , 盖钧镒*
南京农业大学大豆研究所 / 国家大豆改良中心 / 农业部大豆生物学与遗传育种重点实验室 / 作物遗传与种质创新国家重点实验室,江苏南京210095
GAI Jiang-Tao, ZHAO Tuan-Jie, LI Yan* , GAI Jun-Yi*
图6 盐胁迫下南农1138-2、科丰1号幼苗叶片A和根B中 GmADK 基因的相对表达量 误差线表示3次重复的标准误。分别对2个品种南农1138-2、科丰1号作LSD多重比较分析, 根据α=0.05对每个品种在盐胁迫不同时间后的相对表达量分等级, 南农1138-2的等级用大写字母表示, 科丰1号的等级用小写字母表示。
Fig. 6 Relative expression of GmADK in leaves A and roots B of Nannong 1138-2 and Kefeng-1 under salt stress Error bars represent the standard error of three replicates. Least Significant Difference LSD tests were performed for each cultivar α=0.05, the groups were labeled using letters in capital case for Nannong 1138-2 and lower case for Kefeng-1.
Fig. 6 Relative expression of GmADK in leaves A and roots B of Nannong 1138-2 and Kefeng-1 under salt stress Error bars represent the standard error of three replicates. Least Significant Difference LSD tests were performed for each cultivar α=0.05, the groups were labeled using letters in capital case for Nannong 1138-2 and lower case for Kefeng-1.