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No Cross Contamination
The samples are homogenized (or mixed)
non-invasively. The sample tubes are kept closed during
agitation, as the samples are processed. There are no probes to
clean between samples.
> Samples Stay Cool
The instrument uses very little power due to the
unique, patented design. It uses a small DC motor to agitate the
individual tubes, not ultrasonics. Also, because the motor
does not need to agitate any heavy platforms or plates, it is small and
will last for years.
> Convenient
to Use
Simply place your roundworms and other tissue samples or
cell cultures and some beads in standard high quality polypropylene
tubes, and load the tubes into the Bullet Blender™.
Set the duration (typically a few minutes) and speed
(vigorousness). There are no probes to clean. And it is
quieter than a sonicator and does not heat up your samples more than a
few degrees!
> Risk Free
Purchase
The Bullet
Blender™ comes with a 30-day
money back guarantee and a two year warranty, with a three year
warranty on the motor. The simple, reliable design enables the Bullet Blenders™ to sell for a fraction
of the price of ultrasonic or other agitation based instruments, yet
provides an easier, quicker technique.
> Protocol development assistance
We can help you use the Bullet
Blender™,
if protocols are lacking for your application. Our Technical
Support staff will advise you on setting up your experiment as well as
troubleshooting the experiments which didn't turn out like you planned.
Potential Applications
- homogenization
- embryos
- larvae
- dauer stage
- adult worms
- dissected portions of worm tissue
- washing prior to homogenization
- permeabilization for in situ staining
The Bullet
Blender™ home page shows the entire family of products and links to
other applications. Protocol for Brain Tissue Homogenization in the Bullet BlenderThe protocol described in this document is for the use of the Bullet Blender™ for the homogenization of Caenorhabditis elegans cultures (larval, dauer, and adult). 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.). Materials Required:worms, aspirator, Bullet Blender™, homogenization buffer, pipettor, microcentrifuge tubes, and 0.5mm zirconium oxidebeads (part number ZrOB05). Instructions:- Harvest worms from culture plate by washing (either with saline or water) into centrifuge tube.
- Centrifuge worm suspension to yield a pellet under the washing liquid (200-500g for five minutes).
- Completely aspirate the supernatant liquid.
- Inspect the volume of the pellet. It should be 300μL or less in order to get efficient homogenization.
- Add an equal volume of zirconium oxide beads (0.5mm) to the tube. One scoop of beads ≈ 50μL.
- Add 0.1mL to 0.6mL buffer (2 volumes of buffer for every volume of worms).
- Close the microcentrifuge tubes.
- Place tubes into the Bullet Blender™.
- Set controls for SPEED 8 and TIME 2 to 3 minutes.
- Remove tubes from the instrument.
- Visually inspect samples, if homogenization is unsatisfactory, run for another two minutes at the SPEED 10.
- Proceed with your downstream application.
SAFETY NOTE!!!When using a centrifuge to separate your homogenate from the debris and beads, make sure your tubes are balanced.
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