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The media were poured into Petri dishes.
After preparing, PDAD media were poured in a petri dish (P5) and left to set.
Under inert atmosphere the nutrient agar media were poured aseptically into sterilized petri dishes in laminar flow.
The nutrient media were poured into 30 ml tubes.
To investigate genetic variation in oviposition-related decisions, we used a two choice assay: two media were poured side-by-side in a 35 mm petri plate lid, and this lid was presented overnight to single mated females inside a 170 cc plastic arena.
Twenty-mL aliquots of the seeded agar media were poured into 9-cm Petri plates.
Similar(52)
Mueller hinton agar (MHA) was prepared by dissolving 38 g in 1 litre of distilled water, boiling the mixture for 1 min, after cooling and autoclaving, the media was poured into petri dishes.
Diffusion controlled release of TiO2 nanoparticles loaded with streptomycin were studied by dialysis method wherein 10 mg of streptomycin dissolved in 2 µL PBS solution at pH 7.4 (release media) was poured into the inner tube of the dialyzer.
A layer of agar containing 2 ml of 0.5% low melting agar (Bio-Rad) dissolved in growth media was poured into wells of a 6 well cell culture dish and allowed to set at 4°C for 20 minutes.
Nutrient agar media was poured in Petri plates in laminar flow and allowed to solidify for 20 minutes.
Approximately 5 ml of the sterilized media was poured onto the dishes (65 × 15 mm), in an aseptic environment.
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