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The samples were placed on the agar surface for one minute to allow complete hydration and complete contact before detachment.
One 10 μg imipenem and one 30 μg ceftazidime disks were placed on the agar plate.
The percentage of infectious propagules that grew on the agar plates is graphed below.
Spots showed up on the agar as individual bacteria grew and multiplied.
Using a microdissection apparatus equipped microscope suitable for yeast (Singer Instruments), cells were transferred to defined places on the agar plates and virgin daughter cells were collected.
Multiple regression analysis indicated that plasma treatment at 40 W for 25 min is most effective for inhibiting growth of A. flavus on the agar medium.
Reason – this solution contains the bacteria that will grow on the agar.
Filter paper discs containing predetermined concentrations of M. persimmonesis were placed on the agar surface.
MBC were read as concentrations where no bacterial growth occurred on the agar plates [17].
Bacterial viability was assessed by counting the number of colonies formed on the agar plate.
Different concentrations of sLOX-1 were applied on the agar plates.
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CEO of Professional Science Editing for Scientists @ prosciediting.com