User:Dhea Patel/Notebook/CHEM 572: ADA&Inhibitor Kinetics/2013/02/20: Difference between revisions
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==ADA Kinetic Assay for obtaining the zero point== | ==ADA Kinetic Assay for obtaining the zero point== | ||
* The procedure is taken from [[User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/02/20 Mary Mendoza]] | * The procedure is taken from [[User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/02/20|Mary Mendoza.]] | ||
* The objective of this laboratory period is to conduct adenosine deaminase (ADA) kinetic assay runs for the new calculated concentrations. | * The objective of this laboratory period is to conduct adenosine deaminase (ADA) kinetic assay runs for the new calculated concentrations. | ||
* UV 2550 Shimadzu spectrophotometer was baseline with 0.05 M sodium phosphate buffer. | * UV 2550 Shimadzu spectrophotometer was baseline with 0.05 M sodium phosphate buffer. |
Revision as of 12:26, 22 February 2013
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Aspirin concentration for ADA Kinetic AssayADA Kinetic Assay for obtaining the zero point
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