Team:Mississippi State/YPD Plate
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Revision as of 13:34, 19 June 2008 by Caleb Dulaney (Talk | contribs)
Preparing YPD Plates
- Prepare 20% Dextrose solution by weighing out 40g Dextrose. Pour into dry beaker. Also get an autoclaved 500ml bottle.
- Add 50ml water to beaker, stirring with stirbar.
- When dissolved, pour contents into graduated cylinder.
- Add water until volume is 200ml.
- Pour contents into 500ml Bottle.
- Get another beaker.
- Add 2.5g yeast extract, 5g Peptone, and 200ml H2O.
- Stir using stirbar.
- When dissolved, pour contents into graduated cylinder.
- Add H2O until volume is 225ml.
- Weigh out 5g Agar, and pour into empty, autoclaved flask.
- Pour contents of graduated cylinder into flask, covering with foil.
- Take both Dextrose solution and Yeast/Peptone/Agar solution to autoclave: 20min, liquid exhaust.
- Go to fume hood on 3rd floor and turn on UV light to sterilize area.
- When autoclave finishes, immediately swirl Yeast/Peptone/Agar solution insuring everything is well dissolved.
- Go to fume hood on 3rd floor.
- Turn off UV light, and turn on normal light.
- Place Bottle and flask into hood.
- Using sterile graduated cylinder, measure out 25ml 20% Dextrose solution.
- Add solution to Yeast/Peptone/Agar solution to get 250ml YPD media.
- Allow to cool to 55C in waterbath.
- Pour plates (7).