User:Puja Mody/Notebook/Chem 571: Gold Nanoparticles/2012/11/13

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* The Adenosine Deaminase Kinetic assay was done by following the Assay [[AU Biomaterials Design Lab:Protocols/ADA Activity Assay| Protocol]]
* The Adenosine Deaminase Kinetic assay was done by following the Assay [[AU Biomaterials Design Lab:Protocols/ADA Activity Assay| Protocol]]
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# The potassium Phosphate Buffer was actually sodium phosphate and was made at a pH of 7.4
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#* We made 50mL of .05M sodium phosphate buffer 
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.05 x .05= .0025 moles
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.0025 moles x 268.07g/1mol = .6702g sodium phosphate in 50 mL H<sub>2</sub>0. Actual amount = .6705. pH of 7.4 was achieve by adding roughly 3 drops of 12M HCl from a glass pasture pipette.
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#*
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Revision as of 14:10, 15 November 2012

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ADA Kinetics and more

Goals

  • Run UV-Vis and AA on HRP/AuNPs samples
  • Adenosine Deaminase Kinetics Assay

Procedure

  • For procedure and data regarding the UV-Vis and the AA of the HRP and gold nanoparticle solutions, please see either Melissa's notebook or Dhea's notebook.
  • The Adenosine Deaminase Kinetic assay was done by following the Assay Protocol
  1. The potassium Phosphate Buffer was actually sodium phosphate and was made at a pH of 7.4
    • We made 50mL of .05M sodium phosphate buffer

.05 x .05= .0025 moles .0025 moles x 268.07g/1mol = .6702g sodium phosphate in 50 mL H20. Actual amount = .6705. pH of 7.4 was achieve by adding roughly 3 drops of 12M HCl from a glass pasture pipette.


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