Decant supernatant and resuspend the pellet in 500 μl of a suitable buffer.
Transfer the yeast solution to a Yeast Lysing Bead Tube.
Homogenize for 5 minutes at 1500 rpm (press preset button).
To remove debris, centrifuge for 5 minutes at 12,000 × g.
Transfer the supernatant to a clean tube for processing or storage.
May be used for: yeast, algae, spores
Helpful Hints:
Longer processing times may be required to homogenize smaller yeasts (i.e. Pichia).
Homogenization can be evaluated by comparing homogenized yeast to a non-homogenized sample under a microscope. Yeast cells that are cracked open will appear dark gray.