User:Elizabeth Ghias/Notebook/Experimental Chemistry/2013/03/04: Difference between revisions
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==Objective== | ==Objective== | ||
To prepare agar plates and to prepare the starter culture of bacteria. | |||
==Description== | ==Description== | ||
<u>Agar Plate Preparation</u> | |||
== | # Agar plate solution was prepared by adding 12.5 g LB and 10 g agar to 500 mL water. | ||
# The plates were autoclaved for one hour | |||
# Once the solution was cooled, 25 mL aliquots were poured into Petri dishes. | |||
#* This made 20 agar plates | |||
==Data==y | |||
No data was collected today | |||
==Notes== | |||
<u>To Do List this Week</u> | |||
* Make additional quaternary ammonium salt films (wed or tues, Noah) | |||
* Crosslink quaternary ammonium salt films (thurs/fri) | |||
* Split the bacteria from the starter culture between the flasks for testing. | |||
* Measure UV Vis of bacteria in starter culture before adding films | |||
* Put films (cut in half) in flasks, then take periodic UV vis throughout the test. | |||
Revision as of 12:24, 4 March 2013
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ObjectiveTo prepare agar plates and to prepare the starter culture of bacteria. DescriptionAgar Plate Preparation
No data was collected today NotesTo Do List this Week
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