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Homogenization of Malanga Root Tuber
Instrument: Bullet Blender
Sample: Xanthosoma sagittifolium
Protocol:
- OPTIONAL: Wash malanga 3x with ~1mL PBS to remove soil and other surface contaminants and debris.
- Cut malanga into long, thin slices of 200mg or less and place each slice into a microcentrifuge tube.
- Add a volume of beads equal to the mass of the malanga. NOTE: 100mg ≅ 100μ
- Close the microcentrifuge tubes and place them into the Bullet Blender®. NOTE: There should be no buffer in the tubes at this point.
- Set controls for SPEED 8 and TIME 4.
- Remove the samples from the Bullet Blender. The malanga should be finely pulverized into a thick paste. If not, run for another three minutes at speed 10.
- Add 2 volumes of buffer to the tube for every mass of sample (ex. for 100 mg malanga add 200mL buffer).
- Close the microcentrifuge tubes and place them back into the Bullet Blender®.
- Set controls for SPEED 8 and TIME 3 minutes. Press Start.
- After the run, remove tubes from the instrument.
- Visually inspect samples. If homogenization is unsatisfactory, run for another three minutes at speed 10.
- Proceed with your downstream application.
Results: