Scientific Industries SI-BG05 Glass Disruptor Beads Bottle for Yeast/Fungi, 0.5mm Diameter, 8oz Capacity

Scientific Industries SI-BG05 Glass Disruptor Beads Bottle for Yeast/Fungi, 0.5mm Diameter, 8oz Capacity Review

Scientific Industries SI-BG05 Glass Disruptor Beads Bottle for Yeast/Fungi, 0.5mm Diameter, 8oz Capacity Feature

• Disruption of bacterial cultures for nucleic acid isolation and downstream processing
• Grinding plant tissue for DNA extractions
• Preparation of cell lysates from yeast or fungi
• Rapid resuspension of pellets
• Dissolution of chemical substances

Spherical lead free soda lime glass beads are commonly used for mechanical disruption of many yeast. Glass beads of a pre-determined size and volume are placed in a 1.5ml or 2.0ml microtube along with a pre-determined sample amount. The closed tube is then shaken vigorously at high speed, causing collisions between the glass beads and sample material. Scientific Industries Disruptor Genie and TurboMix attachment for the Vortex-Genie 2 family of mixers are excellent choices for this process as they both simultaneously agitate and vortex at high speed, dramatically increasing cell or sample disruption. Each can hold up to twelve 1.5 ml or 2.0 ml microtubes at once. The disrupted cells may be removed after shaking for downstream processing. Disruptor Beads, 0.5 mm diameter, are recommended for disruption of yeast or fungi samples. A typical sample ratio would be 50 percent Disruptor Beads to 50 percent of yeast or fungus suspension by volume. This ratio may be adjusted as necessary. Allow head space (20 percent) within the microtube to facilitate disruption action. It is recommended that beads and yeast or fungus suspension be chilled prior to disrupting in order to offset any temperature rise within the microtube. Yeast cells and fungi are generally more difficult to shear than bacterial cells, so increased disruption times may be necessary. Disruption in a cold room with chilled materials for 5 to 7 minutes at highest speed should be sufficient to disrupt the cell sample. Samples should not be run for longer than 10 minutes consecutively to avoid any temperature rise.