User:Megan L. Channell/Notebook/Horseradish/2013/09/24

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(Protocol)
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**The stock solution of pepsin was diluted from 12μM to 2nM using .83μL in 5mL total solution (solution being hemoglobin)
**The stock solution of pepsin was diluted from 12μM to 2nM using .83μL in 5mL total solution (solution being hemoglobin)
**For a reference in the UV-Vis, hemoglobin stock solution was diluted from 10μL to 1mL.
**For a reference in the UV-Vis, hemoglobin stock solution was diluted from 10μL to 1mL.
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==Data==

Revision as of 21:19, 30 September 2013

Biomaterials Design Lab Main project page
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Objective

Use pepsin to cleve the peptide bonds in hemoglobin and observe its catalytic activity with and without pepstatin. The data collected will be used in a future experiment.

Protocol

The procedure for the lab can be found in Dr. Harting's lab notebook.

  • Noted differences:
    • Instead of 1.7 M perchloric acid, it was 1 M of perchloric acid.
    • For the concnetration of pepstatin added, the group decided upon 0.2 μM.
    • The stock solution of pepsin was diluted from 12μM to 2nM using .83μL in 5mL total solution (solution being hemoglobin)
    • For a reference in the UV-Vis, hemoglobin stock solution was diluted from 10μL to 1mL.

Data


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