Sandbox 323: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
Emma Caszatt (talk | contribs) No edit summary |
||
| (6 intermediate revisions by 3 users not shown) | |||
| Line 23: | Line 23: | ||
- Buffers: Sodium Phosphate buffer, Cell Lysis Buffer Tris-HCl, 10X SDS-PAGE Buffer, Re-Suspension Buffer, 1X Wash Buffer, 1X Elution Buffer | - 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 | - Solutions for SDS-Page: Coomassie Blue Stain, and Destain | ||
- Pre-cast SDS-Page Gel | - Pre-cast SDS-Page Gel | ||
== Experimental and Results == | == Experimental and Results == | ||
| Line 68: | Line 69: | ||
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. | ||