Difference between revisions of "YPD Media and Agar"
From Bridges Lab Protocols
Davebridges (Talk | contribs) (Created page with '==Materials== *YPD Medium (Clontech 630409) *Agar (if making plates) *Adenine Hemisulfate if making YPDA. Dissolve to 0.2% and autoclave. ==Preparation== *Weigh out 5g/100 mL o...') |
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*If making rapamycin plates let cool to ~55C add desired amount of rapamycin | *If making rapamycin plates let cool to ~55C add desired amount of rapamycin | ||
*Pour plates, let dry and store in the cold room | *Pour plates, let dry and store in the cold room | ||
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| + | [[Category:Buffers]] | ||
| + | [[Category:Media]] | ||
Revision as of 12:57, 9 October 2009
Materials
- YPD Medium (Clontech 630409)
- Agar (if making plates)
- Adenine Hemisulfate if making YPDA. Dissolve to 0.2% and autoclave.
Preparation
- Weigh out 5g/100 mL of media
- If making plates, add 2g/100mL of bacto-agar
- Stir to dissolve and check that pH is at 5.8
- Autoclave for 15 min at 121C using the liquid cycle
- If making YPDA plates let cool to ~55C add 1.5 mL/100mL adenine
- If making rapamycin plates let cool to ~55C add desired amount of rapamycin
- Pour plates, let dry and store in the cold room
