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Identification of Nematode Trapping Fungus Monacrosporium eudermatum Based on Genetic Diversity Using RAPD Technique

Ali A. Kasim, Maitham Dragh

American Journal of Microbiological Research. 2016, 4(6), 178-180 doi:10.12691/ajmr-4-6-4
  • Figure 1. RAPD-PCR amplification products were separated by agarose gel (1.4%) electrophoresis and detected by ethidium bromide staining. M marker (50-1500), amplified bands ranged between minimum50 bp in OPF-05 to maximum 750bp in OPA-16
  • Figure 2. Amplified bands were analyzed using Quantity one software to analyze size of the bands and relative relationship between primer APO-16 showed higher amplification as well as higher number of bands, while APB-08 was the less one