User:Elizabeth Ghias/Notebook/Experimental Chemistry/2013/04/18

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(Autocreate 2013/04/18 Entry for User:Elizabeth_Ghias/Notebook/Experimental_Chemistry)
Current revision (15:28, 18 April 2013) (view source)
 
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==Objective==
==Objective==
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Added the calculated amounts of protein to the hydrogels + NHS-azide and plated the bacteria for the QAS test
==Description==
==Description==
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==Data==
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<u>Protein Addition</u>
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* Add data and results here...
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# 10 mL of phosphate buffer (ph = 7.6) was placed in a vial (repeat 4 times)
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# A hydrogel + NHS-azide and a stir bar was added to each vial
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# The corresponding amount of protein (see yesterday for calculations) was added to each vial
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# The vials were allowed to stir overnight
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==Notes==
 
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This area is for any observations or conclusions that you would like to note.
 
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<u>Bacterial Testing</u>
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# Each of the QAS films and a PVOH control were soaked in water and cut into small circles. 
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# 50 uL of bacteria was plated on each agar plate. Sterile techniques were used
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# The film sample was placed on the agar plate
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# 5 uL of bacteria was added to each circle/sample
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# The plates were placed in the incubator overnight. 
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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.
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==Data==
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[[Category:Course]]
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No data was collected today
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[[Category:Miscellaneous]]
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==Notes==
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* The QAS films used for testing were being reused from the last bacterial test.  Not all the bacteria could be washed away by ethanol.

Current revision

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Objective

Added the calculated amounts of protein to the hydrogels + NHS-azide and plated the bacteria for the QAS test

Description

Protein Addition

  1. 10 mL of phosphate buffer (ph = 7.6) was placed in a vial (repeat 4 times)
  2. A hydrogel + NHS-azide and a stir bar was added to each vial
  3. The corresponding amount of protein (see yesterday for calculations) was added to each vial
  4. The vials were allowed to stir overnight


Bacterial Testing

  1. Each of the QAS films and a PVOH control were soaked in water and cut into small circles.
  2. 50 uL of bacteria was plated on each agar plate. Sterile techniques were used
  3. The film sample was placed on the agar plate
  4. 5 uL of bacteria was added to each circle/sample
  5. The plates were placed in the incubator overnight.

Data

No data was collected today

Notes

  • The QAS films used for testing were being reused from the last bacterial test. Not all the bacteria could be washed away by ethanol.



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