| ACROSS | DOWN |
| 1 Neutral pH region used by Laemmli to start all of his samples moving at the same time (2 wds) | 1 Region at pH 8.8 used by Laemmli to sort his proteins by size (2 wds) |
| 3 Matrix material for nucleic acid electrophoresis | 2 Provides motive force to samples in gel |
| 5 Using current to move protein bands onto a plastic matrix and then IDing them with antibodies is called this (2 wds) | 4 In this form of electrophoresis, the sample proteins are first separated by charge and then separated by size (2 wds) |
| 6 The point in a pH gradient at which a protein will stop moving | 7 Matrix material for protein electrophoresis |
| 8 This dye which glows under UV is common for visualizing nucleic acids in gel (2 wds) | 9 ___________ focusing uses the inherent charge of proteins to separate them in a gel with a pH gradient |
| 11 What you have to do to visualize samples in gel | 10 Used to neutralize inherent charges of proteins |
| 12 Coommassie Blue is used to visualize proteins, as is this (2 wds) |