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==


==Data==
<u>Agar Plate Preparation</u>
* Add data and results here...


==Notes==
# Agar plate solution was prepared by adding 12.5 g LB and 10 g agar to 500 mL water.
This area is for any observations or conclusions that you would like to note.
# 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


Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.
==Notes==


[[Category:Course]]
<u>To Do List this Week</u>
[[Category:Miscellaneous]]
* 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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Objective

To prepare agar plates and to prepare the starter culture of bacteria.

Description

Agar Plate Preparation

  1. Agar plate solution was prepared by adding 12.5 g LB and 10 g agar to 500 mL water.
  2. The plates were autoclaved for one hour
  3. 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

To Do List this Week

  • 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.