Difference between revisions of "User:Dhea Patel/Notebook/CHEM 572: ADA&Inhibitor Kinetics/2013/01/23"

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(Experimental Protocol)
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==Experimental Protocol==
'''Protocol for 0.1 M Sodium Phosphate Buffer (pH 7.4)'''
*Add 3.1 g of NaH<sub>2</sub>PO<sub>4</sub>•H<sub>2</sub>O and 10.9 g of Na<sub>2</sub>HPO<sub>4</sub> (anhydrous) to distilled H<sub>2</sub>O to make a volume of 1 L.
**The pH of the final solution will be 7.4.
**This buffer can be stored for up to 1 mo at 4°C.
*Dilute to 0.05M: (take 50 mL of 1M solution and dilute in 1 Liter H<sub>2</sub>O)
'''Running ADA Kinetics'''
*The following table outlines the concentrations and volumes of the solutions used in the ADA kinetics assay to be performed [[User:Dhea_Patel/Notebook/Experimental_Biological_Chemistry_Notebook/2013/01/29| next Tuesday]].
*To prepare a 30 mM stock solution of adenosine:
<math>\frac{0.030mol}{L}</math> of adenosine × <math>\frac{267.24  g}{1  mol}</math> = <math>\frac{8.0172g}{L}</math> of adenosine in buffer
*To make 10mL of solution, 0.080172g of adenosine will be added to 10mL of phosphate buffer.

Revision as of 13:48, 8 May 2013

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