User:Paul Rothenberg/Notebook/Pauls Notebook/2013/02/04

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==Entry title==
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==4 February 2013==
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* Insert content here...
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* Objectives:
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*1. Run UV-VIS and Fluorescence on protein dissolved in Chloroform in Acetate buffer and water in acetate buffer (See Dhea Patel's Notebook - Insert link)
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*2. Use a Lyopholizer to solidify proteins dissolved in solution
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*Lyopholizer Procedure:
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*1. The Lyopholizer was turned on and let cool to -50 Centigrade.
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*2. The proteins were solidified in liquid nitrogen, and placed in the vacuum
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*Fluorescence and UV-VIS Procedure:
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*1. Chloroform and water samples were run in each spectroscope
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2*
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*10 mg of Sorbitol, Hemoglobin, and PEG previously solidifed was added to 5 out of 6 tubes for solvent to be added (See Dhea's Notebook)
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*Data:
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*

Revision as of 14:07, 4 February 2013

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4 February 2013

  • Objectives:
  • 1. Run UV-VIS and Fluorescence on protein dissolved in Chloroform in Acetate buffer and water in acetate buffer (See Dhea Patel's Notebook - Insert link)
  • 2. Use a Lyopholizer to solidify proteins dissolved in solution


  • Lyopholizer Procedure:
  • 1. The Lyopholizer was turned on and let cool to -50 Centigrade.
  • 2. The proteins were solidified in liquid nitrogen, and placed in the vacuum
  • Fluorescence and UV-VIS Procedure:
  • 1. Chloroform and water samples were run in each spectroscope

2*


  • 10 mg of Sorbitol, Hemoglobin, and PEG previously solidifed was added to 5 out of 6 tubes for solvent to be added (See Dhea's Notebook)


  • Data:



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