User:Douglas M. Fox/Notebook/AU CHEM-571 F2011 Lab Support/2014/10/15

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Tasklist SDS-PAGE Warm your samples to about 40 °C using heating block Transfer solutions to a premade gel (2 groups should share a gel...I have 4 - 5 samples as well) Don't forget to use the premade protein ladder Run as previously described Dialysis Be sure to measure protein in solution using Bradford(don't contaminate with the precipitated protein) Set up for next week measure UV & fluorescence of your original colloid solution (run water first to ensure prior protein has been removed)