Sandbox 323: Difference between revisions
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</StructureSection> | </StructureSection> | ||
== Materials == | |||
- Buffers: Sodium Phosphate buffer, Cell Lysis Buffer Tris-HCl, 10X SDS-PAGE Buffer, Re-Suspension Buffer, 1X Wash Buffer, 1X Elution Buffer | |||
- Solutions for SDS-Page: Coomassie Blue Stain, and Destain | |||
- Pre-cast SDS-Page Gel | |||
== Experimental and Results == | == Experimental and Results == | ||
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Fractions E1 through E6 were chosen to be run on an SDS-PAGE gel because they contained the highest amounts of protein. After running for an hour on 100-150 mV, the gel was stained and destained. The bands appeared around 30 kDa and fractions E2-E6 were pure. | Fractions E1 through E6 were chosen to be run on an SDS-PAGE gel because they contained the highest amounts of protein. After running for an hour on 100-150 mV, the gel was stained and destained. The bands appeared around 30 kDa and fractions E2-E6 were pure. The controls include running samples from before and after the column and wash. | ||
