listed below, this declaration becomes invalid.
Device Name: BenchMixer™ Vortex mixer and Mortexer™ Vortex mixer
Device Model Number(s): BV1000-E and BV1005-E and Private label versions of these
Bench Mixer™ Vortexer
Mortexer™ Vortex Mixer
Model BV1005(E) Instruction Manual
The Mortexer™ is MORE than your standard vortexer mixer. The unique design of the Multi-
Head™
Bench Mixer™ Vortexer
Mortexer™ Vortex Mixer
Model BV1005(E) Instruction Manual
The Mortexer™ is MORE than your standard vortexer mixer. The unique design of the Multi-
Head™
Bench Mixer™ Vortexer
Mortexer™ Vortex Mixer
Model BV1005(E) Instruction Manual
The Mortexer™ is MORE than your standard vortexer mixer. The unique design of the Multi-
Head™
Assurance® GDS Vortex Mixer
Assembly
For use with Assurance® GDS assays, remove the standard attachment (gently pull up at the corners) and snap the
microtiter plate attachment onto the vortex mixer (align
therefore, correction factors must be used to calculate the
correct sizing volume for the mixer.
NA-mixers − the following sizes can be selected from the standard range
GMP 50
GMP 100
GMP 500
GMP
combination of a USM Mixer
and a standard NA-Mixer. This is called
Combo mixing.
How to control vortex
• Install the USM Mixer to achieve
vortex, see above.
• Install the NA-Mixer opposite to the
Shear Mixer and a standard
NovAseptic® Mixer. This is called Combo mixing.
How to control vortex
• Install the High Shear Mixer to achieve
vortex, see above.
• Install the NovAseptic® Mixer opposite
Impurities and Chemical
Residues
1. Use clean, dry glassware and PTFE accessories.
2. Use a vortex mixer instead of shaking the tube contents. The latter
action can introduce contaminants from the NMR
Substrate is dissolved with the Buffer solution. If the Substrate does
not dissolve completely, use a vortex mixer or a ultra sonic bath.
- Enzyme working solution
Pipette to mix Enzyme solution, and take
severely damage the vessel.
Sterilizing in Place (SIP)
GMP mixers are designed for SIP.
Sterilization by Pressurized Steam
The mixer can be intermittently operated during the initial
condensate
gentle rocking in a mixer, then carefully remove the supernatant without touching the beads.
6. Add 200 µl Blocking Buffer, incubate for 5 minutes with gentle rocking in a mixer and then carefully remove
Required
Other necessary materials not provided include:
Media per Appendix A
Autoclave
Vortex mixer
Analytical balance, tolerance ± 0.2 g
Stomacher / Masticator machine
Stomacher-type
incubator for use during confirmation if
necessary.
e. Place sealed sample wells on the vortex mixer and vortex at approximately 900 rpm for 5-15 min. If
necessary, adjust rpm to be certain that liquid
overnight at 2–8 °C
on a nutator mixer.
2. Add Protein A/G beads (∼100 µl, prewashed with
PBS) to the mixture and incubate for 1 hour at
2-8 °C on a nutator mixer. Collect the beads by
centrifuging
d. Vortex or shake tube(s) vigorously for 10 minutes at room temperature.
* To obtain high yields, ensure that plasma/buffer solution is mixing vigorously in tube(s). A
vortexing mixer with a
(surface rolling, no splashing) ¤ Violent (surface rolling and splashing)
¤ Vortex is needed ¤ No Vortex ¤ Vortex is not an issue
Comments………...............................................
e. Place sealed sample wells containing Sample Concentration Reagent and sample on the vortex mixer and
vortex at 900 rpm for 10 – 20 min. If necessary, adjust rpm to be certain that liquid does not
samples to a new strip. Return samples to
incubator.
e. Place sealed sample wells on the vortex mixer and vortex at approximately 900 rpm for 10 – 20 min. If
necessary, adjust rpm to be certain that liquid
e. Place sealed sample wells containing Sample Concentration Reagent and sample on the vortex mixer and
vortex at 900 rpm for 10 – 20 min. If necessary, adjust rpm to be certain that liquid does not
Reconstitute the RSE with 5 mL of endotoxin-free water
- Mix intermittently for 30 minutes using a vortex mixer at maximum speed
- Divide stock solution into 50 μL aliquots, into endotoxin-free microcentrifuge
incubator for use during
confirmation if necessary.
5. Place sealed sample wells on the vortex mixer and vortex at approximately 900 rpm for 10–20 min. If
necessary, adjust rpm to be certain that liquid
incubator for use during
confirmation if necessary.
e. Place sealed sample wells on the vortex mixer and vortex at approximately 900 rpm for 10–20 min. If
necessary, adjust rpm to be certain that liquid
wells. Immediately return samples to incubator.
e. Place sealed sample wells on the vortex mixer and vortex at approximately 900 rpm for 10–20 min. If
necessary, adjust rpm to be certain that liquid
strip.
f. Place sealed sample wells containing Concentration Reagent and sample on the vortex mixer and vortex
at 900 rpm for 10 – 20 min. If necessary, adjust rpm to be certain that liquid does not