Notes on the protocol: This protocol does not specify a particular buffer - you may choose which is most appropriate for your downstream application (nucleic acid isolation, protein extraction, etc.).
One of these Bullet Blenders
Bullet Blender (BBX24)
Bullet Blender Blue (BBX24B)
Bullet Blender Storm 24 (BBY24M)
Bullet Blender 24 Gold (BB24-AU)
2 x volume of sample
PINK bead lysis kit (PINK) (for samples up to 100 mg.)
RED bead lysis kit (RED) (for samples between 100 and 300 mg.)
0.5 mm zirconium oxide beads (ZROB05) Use a volume of beads equivalent to 1 x the volume of the sample
If your sample has been grown on a plate or other solid surface, detach it (e.g, by flooding the plate with PBS and scraping) and place the material in a microcentrifuge tube. Liquid cultures may be placed directly in the tube as long as they are of sufficient density.
Centrifuge the suspension to yield a pellet. The pellet should be no larger than 300 ul.
Pipette off the supernatant, and resuspend the pellet in 2 volumes of homogenization buffer.
Place the sample in the tube with the beads.
Close the tubes tightly and place them in the Bullet Blender.
Set the controls for Speed 10 and Time 3. Press Start.
After the run, remove the tubes from the instrument and visually inspect the samples. If homogenization is incomplete, repeat the homogenization step at a higher speed.