User:Michael S. Bible/Notebook/571/2014/10/08

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Run Bradford Analysis on Post-Dialysis Solutions

Post-dialysis solutions from all of the wells in the dialysis chamber were analyzed using UV-Vis using the following protocol:

  • Remove 20 μL of solution from each chamber (10 in all) and run Bradford analysis
    • Bradford reagent should be diluted 1:4 with water.
    • Recall, 20 μL solution + 200 μL diluted Bradford + 780 μL Tris/NaCl buffer
    • PS cuvettes, measuring 400 - 800 nm
    • Run a blank with just Bradford & buffer


Procedure taken from Dr. Fox

Run Ca2+ ISE on Dialyed Samples

  • Place the contents of each dialysis well in a scintillation vial.
  • Use the ISE probe to measure the potential of each solution.
  • Use values obtained along with the equation from the Ca2+ Calibration Curve to determine the final concentration of Ca2+ in the solutions.

Data

Ca2+ ISE Data

Above are the final concentrations of Ca2+ in the post-dialysis solutions. The final two initial concentrations do not give good data as the final concentrations measured between the protein and ion side add to a greater concentration of ions than was originally present in the initial solution. These two data points should be disregarded and Lysozyme should be dialyzed against additional concentrations of Calcium ions in order to form a better curve later.

Bradford Data

Above are the results of Bradford anlysis of the post-dialysis protein solutions. The data does not look good, and suggests that there is no protein present. The most likely reason for such data is that the wrong side of the dialysis chamber was tested using Bradford Analysis. The samples are still stored from this experiment, so it may be possible to re-run this UV-Vis experiment.

Notes

This area is for any observations or conclusions that you would like to note.


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