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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 muscle tissue 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.
> Established Protocols
Protocol for Striated Muscle Tissue Homogenization in the Bullet Blender™
The protocol described in this document is for the use of the Bullet Blender™ for the
homogenization of striated / skeletal muscle tissue (from a variety of animals). Note
that the time and speed settings may differ due to the variation in consistency/texture
of tissue from species to species. 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:
muscle tissue, Bullet Blender™, homogenization buffer,
pipettor, microcentrifuge tubes, and 0.5mm zirconium oxide beads (part
number ZrOB05).
Instructions:
- Cut muscle tissue into appropriately sized pieces for analysis (50mg-300mg)
and place into a microcentrifuge tube. Typical sample size: 200mg.
- OPTIONAL: Wash tissue 3x with ~1mL PBS. Aspirate. NOTE: This step
removes external contaminants (blood, etc.).
- Add zirconium oxide beads (0.5mm) to the
tube. Use a mass of beads equal to 1.5x to 2x your mass of tissue. One scoop of zirconium oxide beads ≈ 190mg.
- Add 0.1mL to 0.6mL buffer (2 volumes of buffer for every mass of tissue).
- Close the microcentrifuge tubes.
- Place tubes 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
two minutes at the SPEED 10.
- Proceed with your downstream application.
Bullet Blender™ 50 Homogenization Protocol for Striated Muscle
The protocol described in this document is for the use of the Bullet Blender™ 50 for the
homogenization of Striated / Skeletal Muscle Tissue. 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:
Muscle , Bullet Blender™ 50, homogenization buffer, pipettor,
50mL centrifuge tubes, 4.8mm or 3.2mm stainless steel beads
(part number SSB48 or SSB32).
Instructions:
- Cut adipose into appropriately sized pieces for analysis (0.1g – 3g) and place into a
50mL centrifuge tube.
- OPTIONAL: If desired, wash the tissue 3x with 5mL PBS to remove blood and
other contaminants from the tissue.
- Add two times as much 4.8mm or 3.2mm stainless steel beads (by mass) as you
have sample (so for 1g sample, add 2g beads). A 3.2mm bead weighs 136mg. A 4.8mm bead weighs 457g.
- Add two volumes of buffer per mass of tissue (2mL of buffer per gram of tissue)
- Tightly screw the centrifuge tubes closed.
- Place tubes into the Bullet Blender™ 50.
- Set controls for SPEED 10 and TIME 15 minutes. Press start.
- After the run, remove the tubes from the instrument.
- Visually inspect samples, if homogenization is unsatisfactory, run for another nine
minutes at 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.
Typical Results
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