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| - | ==Aspirin concentration for ADA Kinetic Assay==
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| - | * The assay for the concentrations below will be conducted next laboratory period.
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| - | [[Image:Screen_Shot_2013-02-19_at_1.13.00_PM.png|center]]
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| - | ==ADA Kinetic Assay for obtaining the zero point==
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| - | * The procedure was taken from [[User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/02/20|Mary Mendoza.]]
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| - | * The objective of this laboratory period is to conduct adenosine deaminase (ADA) kinetic assay runs for the new calculated concentrations.
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| - | * UV 2550 Shimadzu spectrophotometer was baseline with 0.05 M sodium phosphate buffer.
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| - | * The assays were prepared according to the data below.
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| - | [[Image:Screen_Shot_2013-02-19_at_2.46.05_PM.png|center]]
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| - | * After running the first trial, it was observed that the absorbance for 12.34 μM adenosine of trial 2 was superimposed over the 10.52 μM adenosine of trial 1.
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| - | * It was suggested by Dr. Hartings to use Beer's Law for accurate measurement of the concentration of adenosine in solution.
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| - | * An article was provided by Dr. Hartings with the molar extinction coefficient, 1.53 x 10<sup>-4</sup> of adenosine at 260 nm.
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| - | * Thus, it was decided to run a full spectrum of adenosine at each given concentration specified above for accurate measurement of the concentration of adenosine.
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| - | ==Data==
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| - | [[Image:Concen1.png|center]]
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| - | [[Image:AveVelo1.png|center]]
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| - | [[Image:1adeno.png|center]]
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| - | [[Image:Lin1.png|center]]
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| - | [[Image:UV2.20.png|center]]
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