User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/02/12: Difference between revisions
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==ADA Kinetic Assay== | ==ADA Kinetic Assay== | ||
*The assay runs were continued from last week's, [[User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/02/05|02/05/2013]] calculated values. | *The procedure was taken from [[User:Dhea Patel/Notebook/CHEM 572: ADA&Inhibitor Kinetics/2013/02/12|Dhea Patel's]] notebook entry. | ||
*The assay runs were continued from last week's, [[User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/02/05|02/05/2013]], calculated values. | |||
*The objective of performing the assay is to obtain the rate of the enzymatic reaction of adenosine into inosine by ADA. | *The objective of performing the assay is to obtain the rate of the enzymatic reaction of adenosine into inosine by ADA. | ||
*Baseline 200-400nm using pH 7.4, 0.05M phosphate buffer | *Baseline 200-400nm using pH 7.4, 0.05M phosphate buffer | ||
*Temperature control: 25°C | *Temperature control: 25°C | ||
*Phosphate buffer in reference cell | *Phosphate buffer in reference cell | ||
*Ran kinetics on 250uM solution (20uL ADA, 600uL | *Ran kinetics on 250uM solution (20uL ADA, 600uL 1250 uM adenosine, and 2.38mL pH 7.4, 0.05M phosphate buffer) for 5 minutes at 265 nm. | ||
**absorbance exceeded 4.00, so the assay was stopped and a new solution was prepared. | **absorbance exceeded 4.00, so the assay was stopped and a new solution was prepared. | ||
*Ran kinetics on 2.56uM solution (20uL ADA, 600uL 12. | *Ran kinetics on 2.56uM solution (20uL ADA, 600uL 12.8 uM adenosine, and 2.38mL pH 7.4, 0.05M phosphate buffer) for 5 minutes at 265 nm. | ||
**dAbs was obtained and plotted vs. time in excel | **dAbs was obtained and plotted vs. time in excel | ||
*Ran kinetics on 6.4uM solution (20uL ADA, 600uL | *Ran kinetics on 6.4uM solution (20uL ADA, 600uL 32 uM adenosine, and 2.38mL pH 7.4, 0.05M phosphate buffer) for 5 minutes at 265 nm. | ||
**dAbs was obtained and plotted vs. time in excel | **dAbs was obtained and plotted vs. time in excel | ||
*Ran kinetics on 16uM solution (20uL ADA, 600uL | *Ran kinetics on 16uM solution (20uL ADA, 600uL 80 uM adenosine, and 2.38mL pH 7.4, 0.05M phosphate buffer) for 5 minutes at 265 nm. | ||
**dAbs was obtained and plotted vs. time in excel | **dAbs was obtained and plotted vs. time in excel | ||
*The following table describes the volumes and concentrations of the components added to the cuvette. | *The following table describes the volumes and concentrations of the components added to the cuvette. | ||
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[[Image:Data_Table.JPG|center]] | [[Image:Data_Table.JPG|center]] | ||
* Note: Since the 250 μM adenosine assay exhibited a high absorbance, this concentration was replaced with two other adenosine concentrations, 150 and 200 μM. | |||
* The stock solution for 150 μM adenosine was made by diluting 150 μL of 5 mM adenosine into 850 ng/μL of 0.05 M phosphate buffer. The 200 μM adenosine was made by diluting 200 μL of 5 mM adenosine into 800 μL of 0.05 M phosphate buffer. | |||
==Graphs== | |||
[[Image:TableT1.JPG]] | |||
[[Image:Avg_Velocity_T1.JPG]] [[Image:Lineweaver-Burk_Plot_T1.JPG]] | |||
Revision as of 12:51, 13 February 2013
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ADA Kinetic Assay
Graphs
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