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Making Agar Plates
From 2008.igem.org
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Riachalder (Talk | contribs) (New page: ===Basic Agar== * Melt 100ml of nutrient agar in the microwave on low heat until clear. * Leave to cool until the bottle can be handled comfortably. * Mix well by swirling the bottle gent...) |
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* Melt 100ml of nutrient agar in the microwave on low heat until clear. | * Melt 100ml of nutrient agar in the microwave on low heat until clear. | ||
Revision as of 14:46, 8 September 2008
Contents |
Basic Agar
- Melt 100ml of nutrient agar in the microwave on low heat until clear.
- Leave to cool until the bottle can be handled comfortably.
- Mix well by swirling the bottle gently.
- Remove the lid of a sterile petri dish just enough so that the liquid can be poured onto the plate (a 100ml bottle of agar will be enough to pour 4 plates) and slowly pour the liquid agar making sure you do not make it too thin or too thick.
- Remove any bubbles by quickly moving the flame of a bunsen over the poured agar.
- Leave to set at room temperature for around 45 minutes.
- Once set, leave the plates in a fan-cupboard for 10 minutes with their lids partially off to dry out any condensation.
Antibiotic Agar
For positive selection of cells that have the antibiotic resistance gene.
- Add the required antibiotic once the melted agar is cool enough to touch. Be sure to check the stock antibiotic concentration first. For example, for kanamycin of stock concentration 25mg/ml, we added 40μl to the 100ml of nutrient agar.
Starch Agar
For negative selcetion of cells that have interruption of amyE and therefore cannot make amylase.
- Add 1g starch powder and 1g bacterial agarose powder to 100ml LB and proceed to the microwaving stage. This agar does not need to be left to cool before pouring.
Sucrose Agar
For negative selcetion of cells that have interruption of sacA and therefore cannot make sucrase.
Make up the following:
- 100mL SMM (a mixture of essential salts)
- 500μl glutamate (nitrogen source)
- 500μl tryptophan
