Team:GeorgiaTech/Agar Plates and Media Protocol
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(Created page with "*Add (35 g/L of LB Agar) or (25 g/L LB broth and 15 g/L Agar) to a flask with distilled water *Dissolve and autoclave for 30 mins (Basement lab [[Autoclave ...")
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(Created page with "*Add (35 g/L of LB Agar) or (25 g/L LB broth and 15 g/L Agar) to a flask with distilled water *Dissolve and autoclave for 30 mins (Basement lab [[Autoclave ...")
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Revision as of 19:54, 27 September 2013
- Dissolve and autoclave for 30 mins (Basement lab autoclave machine) or 1 hour ( Barker lab autoclave machine)
- Antibiotics should be added at the correct concentration and volume when the agar has cooled to around 50°C or cool enough for hands to be touching the exterior of the flask.
- Concentrations of antibiotics:
- Chloramphenicol 34 µg/µL - Blue
- Kanamycin 50 µg/µL - Green
- Ampicillin 100 µg/µL - Red
- For every mL of LB agar solution, add 1 µL of antibiotics.
- Since I was using 300 mL of water, I added .3 mL of kanamycin
- The plates are poured and cooled, then marked with a marker to signify the antibiotic.
- Agar stabs are from the same protocol, just poured into tubes and capped.
- Media solution is made from LB broth (25 g/L), autoclaved, and antibiotics added to it.
- From the toothpick used to create an agar stab, the toothpick is placed into the media solution to start the culture.