《Table 1 qRT-PCR primers of MdCER family》

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《"The Characterization, Authentication, and Gene Expression Pattern of the MdCER Family in Malus domestica"》

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Total RNA was extracted using an RNA plant reagent（Tiangen，China）.The RNA（1–7μg）was reverse-transcribed using the Prime Script first-strand cDNA synthesis kit（Ta Ka Ra，China）.Quantitative real-time（q RT）PCR was used to detect the expression level of the Md CER family in different apple organs and in response to ABA and PEG.Md Actin（GenBank accession number:CN938024）was selected as an internal control gene.All of the primers are shown in Table 1.The results were based on the average of three parallel experiments.