Neoheteromita globosa Howe et al.

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ATCC recommends that individuals contemplating commercial use of any culture first contact the originating investigator to negotiate an agreement.  Third party distribution of this culture is discouraged, since this practice has resulted in the unintentional spreading of contaminated cultures.

2.   Inoculate a T-25 tissue culture flask containing 10.0 ml of bacterized ATCC medium 802 with 0.1 ml from a predominantly encysted Heteromita globosa culture.

3.   Incubate at 25°C with cap screwed on tightly.

4.   For routine maintenance subculture every 10-14 d.

2.  Adjust the concentration of cells to 2 x 10⁶ - 10⁷/ml in fresh medium.

3.  While cells are centrifuging prepare a 20% (v/v) solution of sterile DMSO in fresh medium.

a) Add 2.0 ml of DMSO to an ice cold 20 x 150 mm screw-capped test tube;

b) Place the tube on ice and allow the DMSO to solidify (~5 min) and then add 8.0 ml of ice cold medium;

c) Invert several times to dissolve the DMSO;

d) Allow to warm to room temperature.

4.  Mix the cell preparation and the DMSO in equal portions. Thus, the final concentration will be 10⁶ - 10⁷ and 10% (v/v) DMSO. The time from the mixing of the cell preparation and DMSO stock solution before the freezing process is begun should be no less than 15 min and no longer than 30 min.

5.  Dispense in 0.5 ml aliquots into 1.0 - 2.0 ml sterile plastic screw-capped cryules (special plastic vials for cryopreservation).

6.   Place the vials in a controlled rate freezing unit.  From room temperature cool at -1°C/min to -40°C.  If the freezing unit can compensate for the heat of fusion, maintain rate at        -1°C/min through the heat of fusion.  At -40°C plunge into liquid nitrogen. Alternatively, place the vials in a Nalgene 1°C freezing apparatus.  Place the apparatus at -80°C for 1.5 to 2 hours and then plunge ampules into liquid nitrogen.  (The cooling rate in this apparatus is approximately -1°C/min.)  

7.  The frozen preparations should be stored in either the vapor or liquid phase of a nitrogen refrigerator. Frozen preparations stored below -130°C are stabile indefinitely. Those stored at temperatures above -130°C are progressively less stabile as the storage temperature is elevated. If frozen material is to be stored at temperatures between -130°C and -70°C the shelf life should be empirically tested, i.e., remove stored material at intervals to determine die-off rate.

8. To establish a culture from the frozen state place an ampule in a water bath set at 35°C. Immerse the ampule to a level just above the surface of the frozen material. Do not agitate the ampule.

9. Immediately after thawing, do not leave in the water bath, aseptically remove the contents of the ampule and inoculate a T-25 tissue culture flask containing 10 ml of bacterized ATCC medium 802.

10.          Incubate with the cap screwed on tightly at 25°C.