Team:Glendale CC AZ/Protocols/SurivalGrowth
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+ | == Survival Growth Assay == | ||
+ | |||
+ | |||
+ | == Materials == | ||
+ | |||
+ | -P200 micropipette | ||
+ | -10 microliters bacteria | ||
+ | -90 mictroliters LB media | ||
+ | -Agar plates with appropriate antibiotic | ||
+ | -Spreader | ||
+ | -20mL ethanol (to sterilize spreader) | ||
+ | -Incubator set to 37 degrees celcius. | ||
+ | |||
+ | |||
+ | == Procedure == | ||
+ | |||
+ | 1. Label all plates (Keep upside down to avoid condensation on agar) | ||
+ | 2. Pipette LB media into tube containing bacteria; aspirate. | ||
+ | 3. Using P200 micropipette, extract all 100 microliters of solution and place onto appropriate agar plate. | ||
+ | 4. Briefly flame the spreader and let cool momentarily. | ||
+ | 5. Spread bacteria-LB solution all over plate. | ||
+ | 6. Incubate at 37 degrees celcius for up to 24 hours. |
Revision as of 18:58, 11 August 2013
Survival Growth Assay
Materials
-P200 micropipette -10 microliters bacteria -90 mictroliters LB media -Agar plates with appropriate antibiotic -Spreader -20mL ethanol (to sterilize spreader) -Incubator set to 37 degrees celcius.
Procedure
1. Label all plates (Keep upside down to avoid condensation on agar) 2. Pipette LB media into tube containing bacteria; aspirate. 3. Using P200 micropipette, extract all 100 microliters of solution and place onto appropriate agar plate. 4. Briefly flame the spreader and let cool momentarily. 5. Spread bacteria-LB solution all over plate. 6. Incubate at 37 degrees celcius for up to 24 hours.