Difference between revisions of "User:Elizabeth Ghias/Notebook/Experimental Chemistry/2013/03/04"

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==Description==
 
==Description==
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<u>Starter Culture Preparation</u>
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# Make one solution of 1.875 g LB broth in 75 mL water and make 8 solutions of 1.25 g LB broth in 50 mL water
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# Cap all with foil
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# Autoclave solutions for one hour
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# For the 75 mL solution, take out 4 mL broth and put into 4 test tubes
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# To each tube, add bacteria by scraping frozen bacteria (BL21 E. coli) with a micropipette tip (should be about 5 uL). Do this in a sterile environment (flame)
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# Place the tubes on a shaker at 37°C overnight.
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<u>Agar Plate Preparation</u>
 
<u>Agar Plate Preparation</u>
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# The plates were autoclaved for one hour
 
# The plates were autoclaved for one hour
 
# Once the solution was cooled, 25 mL aliquots were poured into Petri dishes.  
 
# Once the solution was cooled, 25 mL aliquots were poured into Petri dishes.  
#* This made 20 agar plates
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#* This made about 20 agar plates
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# The plates were left in the fridge to set
  
  
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==Notes==
 
==Notes==
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* Because of snow day this week, bacteria were left on shaker until Thursday.
  
 
<u>To Do List this Week</u>
 
<u>To Do List this Week</u>

Revision as of 12:31, 8 March 2013

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Objective

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

Description

Starter Culture Preparation

  1. Make one solution of 1.875 g LB broth in 75 mL water and make 8 solutions of 1.25 g LB broth in 50 mL water
  2. Cap all with foil
  3. Autoclave solutions for one hour
  4. For the 75 mL solution, take out 4 mL broth and put into 4 test tubes
  5. To each tube, add bacteria by scraping frozen bacteria (BL21 E. coli) with a micropipette tip (should be about 5 uL). Do this in a sterile environment (flame)
  6. Place the tubes on a shaker at 37°C overnight.


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 about 20 agar plates
  4. The plates were left in the fridge to set


Data

No data was collected today

Notes

  • Because of snow day this week, bacteria were left on shaker until Thursday.

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.
  • DSC data analysis