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Aug 06, 2020 · Then 1 mL of the growth media with 0.1% of raw, cooked, and vacuum-prepared honey was added. Pictures were taken at time 0, 4, 8, and 24 h (6 h for the insert condition). Each experiment was done

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Insert the sterile pipette tip into the vial and aspirate 0.1 mL of PBS. Remove the pipette from the vial, replace the cap, and set it aside. Carefully hold the pipette, do not touch the tip or lay the pipette on the bench top. With your free hand, pick up the lid to the petri dish and hold it at an angle over the plate.

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