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从筛选出的差异表达基因中随机挑选了6个与伸展蛋白相关的差异表达基因9个与AGPs相关的差异表达基因进行荧光定量PCR验证。结果证实，这15个基因的表达量均不同程度的响应了...
从筛选出的差异表达基因中随机挑选了6个与伸展蛋白相关的差异表达基因9个与AGPs相关的差异表达基因进行荧光定量PCR验证。结果证实，这15个基因的表达量均不同程度的响应了香蕉伤根及接菌处理。其中，基因LOC103997407、LOC103991051对香蕉伤根及接菌处理的响应明显高于其它基因。
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从筛选出的差异表达基因中随机挑选了6个与伸展蛋白相关的差异表达基因9个与AGPs相关的差异表达基因进行荧光定量PCR验证。结果证实，这15个基因的表达量均不同程度的响应了香蕉伤根及接菌处理。其中，基因LOC103997407、LOC103991051对香蕉伤根及接菌处理的响应明显高于其它基因。
Randomly selected from the screening of differentially expressed genes in six differentially expressed genes related to extensin nine of differentially expressed genes related to AGPs fluorescence quantitative PCR verification. Results confirmed that the 15 gene expression quantity response to different extent the banana root damage and the inoculation treatment. Among them, genetic LOC103997407, LOC103991051 on the banana roots and the response of the inoculation treatment was obviously higher than that of other genes.
Randomly selected from the screening of differentially expressed genes in six differentially expressed genes related to extensin nine of differentially expressed genes related to AGPs fluorescence quantitative PCR verification. Results confirmed that the 15 gene expression quantity response to different extent the banana root damage and the inoculation treatment. Among them, genetic LOC103997407, LOC103991051 on the banana roots and the response of the inoculation treatment was obviously higher than that of other genes.
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