Molecular verification of VdCYC8 deletion mutants, and comparison of in vitro growth of wild type strain Vd080 and the CYC8 deletion mutant strains (ΔCYC8-45, ΔCYC8-55, ΔCYC8-56).
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https://figshare.com/articles/dataset/_Molecular_verification_of_VdCYC8_deletion_mutants_and_comparison_of_in_vitro_growth_of_wild_type_strain_Vd080_and_the_CYC8_deletion_mutant_strains_CYC8_45_CYC8_55_CYC8_56_/1618175
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A) PCR verification of vdCYC8 deletion mutants with primer CYC8test-F/R. Lanes 1–6 indicate PCR from DNA template extracted from strains ΔCYC8-45, ΔCYC8-55, ΔCYC8-56, Vd080, T286, and the positive control pGKO2-CYC8 plasmid, respectively. The molecular weight marker (M) is 1kb ladder. B) Tested with primer Hyg-F/R. C) Reverse-transcription PCR analysis of CYC8 expression in strains ΔCYC8-45 (lane 1), ΔCYC8-55 (lane 2), ΔCYC8-56 (lane 3), Vd080 (lane 4), T286 (lane 5), respectively. The V. dahliae β-tubulin (Bt), amplified using primers VerBt-F/R, is shown as a control. D) Characteristics of growth of different isolates of the V. dahliae CYC8 mutant strains on PDA.
创建时间：
2016-02-22
