Full Baffle TUNAIR™ Shake Flask, 2.5L – 4 Pack
- Part number includes a 4-pack of 2.5L Full-Baffle TUNAIR Shake Flasks. Caps and filters are not included.
The TUNAIR™ Shake Flask Systems are a unique and patented flask and closure system, designed for microbiology and biotechnology applications. The full baffle TUNAIR shake flask provides optimum growth conditions for aerobic microorganisms, mammalian cells, and plant cells. They also provide better culture growth and productivity than standard Erlenmeyer flasks. The TUNAIR™’s high oxygen absorption rate is due to the unique baffling and turbo-vane closure design. The TUNAIR™ systems are designed to increase the availability of dissolved oxygen as well as improve cell yields.
The Full Baffle Shake Flask has six baffles that produce a propeller motion. The working volume is 1L.
The flasks are constructed of polypropylene and resistant to most solvents.
All TUNAIR™ flasks and caps can be cleaned by soaking in water with a light detergent solution to loosen dirt and contaminants, then air dry.
Caps and filters are not included in this product number.
Flask Size: 2.5L
Working Volume: 1L
Base Diameter: 6.50” [16.51cm]
Neck Diameter: 3.00” [7.62cm]
Height: 10.75” [27.31cm]
Weight: 0.02 lbs. [0.008Kg]
Full-Baffle (6 Baffles): Propeller Motion
1” Throws: 300-400rpm or possibly higher
2” Throws: 150-200rpm or possibly higher
All TUNAIR flasks and caps are constructed of chemical resistant polypropylene. All flasks and caps are fully autoclavable.
All TUNAIR flasks and caps can be cleaned by soaking in water with a light detergent (i.e. Joy) solution to loosen dirt and contaminants; air dry. All TUNAIR flasks and caps can be autoclaved, if required.
Cell Growth Evaluation of Commonly Used Shake Flasks
TUNAIR™ flasks were compared to conventional flasks using four different types of microorganisms; Escherichia coli, Saccharomyces cerevisiae, Penicillium avellaneum, and Streptomyces chartreusis. The aeration capacities of the shake flasks were determined by the sulfate oxidation method, and the values shown below are presented as oxygen absorption rate (OAR) in mM oxygen/L/Min. The growth rates of E.coli and S.cerevisiae were expressed as optical densities (OD) at 555mM. For S.chartreusis and P.avellaneum growth rates were evaluated by percent sedimentation. For E.coli and S.cerevisiae, the growth rates were determined after an 18-hour incubation period; for S.charteusis, a 24-hour incubation period; and for P.avellaneum, a 72-hour incubation period. Growth and OAR evaluations were carried out with 3-9 replicates and statistically analyzed using Turkey’s w-procedure. See results below.
|OAR Value||OD @ 555mM||% Sedimentation|
|Triple Indented Flasks||2.47||5.97||5.31||19.20||9.50MP|
*Growth Morphology: M, mycelial; P, pellet; MP, mixed mycelial. The mycelial growths mostly adhered to the walls of the flask, which accounted for the low overall sedimentation value.