User:Elizabeth Ghias/Notebook/Experimental Chemistry/2013/03/07
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<u>Agar Plate Preparation</u> | <u>Agar Plate Preparation</u> | ||
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| + | * 50 mL of bacteria was pipetted onto each plate | ||
| + | * The inoculation loop was placed in ethanol and then placed through a flame. | ||
| + | * The loop was then used to spread around the bacteria. | ||
| + | * Samples were then added to the bacteria (see above). For the samples containing half of a film, the flattest portions of the films were used. Tape was used to try and push the films flat against the surface of the plate | ||
| + | * The plates were then covered and placed in an oven set to 37°C overnight. | ||
| + | * The films will be visualized on Friday. | ||
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==Notes== | ==Notes== | ||
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| - | + | * Sterile techniques were used for all of these tests (flame) | |
| - | + | * The tape was ineffective at holding the film against the plate b/c it could not stick to the plate. It also blocked portions of the sample and made visualization more difficult. | |
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ObjectiveTo inoculate the agar plates and the previously autoclaved LB broth for bacterial testing DescriptionLB broth large flask testing
DataUV Vis Data
Notes
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