ライブ固定化酵母細胞の可視化のための高速手法

The aim of the Experiment is to be able to follow a population of providing sir one cells under the microscope so that I can see how the epigenetics states change how often the epigene states change with each, with each successive division of the cells, take a long cover slip, take about seven microliters of cells, place on the long cover slip and use a com, a synthetic media plate. Take a razor blade and then make cuts into the agar. So take an agar block, lift it up and place over the cells.

Okay, for short term experiments, up to three hours. This by itself is fine. The cells will be immobilized for longer term experiments, I add li liquid medium to the top of the agar pad, and then put a glass slide over top of the whole thing.

The media will provide us like a seal between the two. The, the slide is solely to prevent evaporation from the top of the of the agar block. So with this setup, the egger block will remain moist and the cells will continue dividing for up to eight, at least up to eight hours.