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If the plates are unused, just wrap them up and throw them out. They aren't hazardous.

If they are used, you need to decontaminate them before disposal. If you don't have access to an autoclave, my recommendation would be to open them in a big beaker or other big container and submerge them in full strength bleach for a few hours to overnight (wear gloves). You can dispose of the bleach down the sink and them re-close the plates, wrap them in saran wrap and throw them out. Its not a perfect solution, but for three plates it will do.

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13y ago
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12y ago
1. Bleach Method1. Add 1 to 2 milliliters of bleach to each test tube. Allow the bleach to contact the test tube for 15 minutes, then pour the liquid down a drain.

2. Make a water bath containing 10 percent bleach, and soak the instruments for at least one hour.

3. Pour the solution down a drain and allow the instruments to dry completely before re-using.

2. Autoclave Method1. Place the contaminated instruments in unsealed biohazard bags so the bacteria doesn't leak into the autoclave. Make sure the bags are open so steam can escape.

2. Turn on the autoclave to 15 pounds per square inch (psi) at 121 degrees C for 30 minutes.

3. Allow the biohazard bags to cool. Seal the bags and place in a tightly secured garbage bag. Dispose of the garbage bag.

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11y ago

Disinfect the plate by adding 200-300ml of 10% bleach to the plate; wait for at least one hour; dispose the plate.

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13y ago

put it in your shoe

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Q: How do you dispose of inoculated agar plates?
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Why the inoculated agar medium plate must be inverted position in incubator?

Moisture in the air condenses on the lid of the plate and drops on top the agar if the plates are place right way up. The falling water droplets will spread the bacteria and especially ruin streak plates and spead plates where you need clear distict separate colonies.


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Yes, you can streak some green algae of agar, but you have to known the nutrients you need to add to the agar. For instance Chlamydomonas reinhardtii can be grown on TAP plates, or on high salt plates.


Prewarm agar plates?

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Why do streak plates need to be dry before inoculated?

If by inoculated you mean used, here is my answer if that is true; streak plates need to be dry because the powder left behind may react and change color to whatever that liquid is on the streak plate.


Why did you stab the peptone iron agar instead of inoculating only the surface?

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